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Review

Vegetable Salad Improves Lipid and Glucose Metabolism and Enhances Absorption of Specific Nutrients in Vegetables

1
Department of Public Health Nutrition, Faculty of Public Health, Universitas Indonesia, Depok 16424, Indonesia
2
Asian Nutrition and Food Culture Research Center, Jumonji University, Niiza 352-8510, Japan
3
Jakarta Sales Office, PT Kewpie Indonesia, Jakarta Selatan 12520, Indonesia
4
R&D Division, Kewpie Corporation, Tokyo 182-0002, Japan
5
Department of Food and Nutrition, Jumonji University, Niiza 352-8510, Japan
*
Author to whom correspondence should be addressed.
Foods 2024, 13(22), 3591; https://doi.org/10.3390/foods13223591
Submission received: 16 October 2024 / Revised: 2 November 2024 / Accepted: 7 November 2024 / Published: 10 November 2024
(This article belongs to the Special Issue The Health Benefits of Fruits and Vegetables—3rd Edition)

Abstract

:
Vegetables are low in energy and rich in vitamins, minerals, and dietary fiber; various health benefits associated with their intake have been reported. Salads are one of the most convenient ways to consume vegetables and can be made simply by pouring mayonnaise, dressing, olive oil, or other condiments over a selection of vegetables. There are also many reports on the ways in which vegetable intake can improve health. However, there is no comprehensive review summarizing the health functions of vegetables when consumed as a salad. The effects of vegetable salads on amounts of vegetable intake, lifestyle-related diseases, and the absorption of specific nutrients through mayonnaise, as well as the effects of the order in which vegetable salad and carbohydrates are consumed, have been reported. In this review, the health functions of vegetable salad consumption are reported.

1. Introduction

Vegetables are herbaceous plants used in various culinary preparations. They are indispensable foods because they are rich in vitamins, minerals, dietary fiber, and phytochemicals necessary for human survival [1].
As the dietary habits of humans have diversified, the prevalence of lifestyle-related diseases and other diseases has increased; therefore, improving dietary habits is important for maintaining and promoting health [2]. One of the possible causes of poor dietary habits is low vegetable intake. It is recommended that Japanese people consume 350 g of vegetables daily, but the vegetable intake of Japanese adults is only ~280 g [3,4]. Although a vegetable intake of 250 g is recommended for Indonesian people, the average daily intake in 2020 was 143 g, falling short of the recommended vegetable intake in both countries [5]. The Indonesian Health Survey in 2023 showed that 96.7% of people consume less fruit and vegetables than recommended [6].
Increased vegetable intake reduces body weight, metabolic syndrome, and the risk of coronary artery disease (Figure 1) [7]. Metabolic syndrome is a complication caused by increased visceral fat, irregular diet, excessive food intake, and a lack of exercise and causes glucose intolerance, hypertension, and dyslipidemia, which are risk factors for arteriosclerotic illness [8]. The consumption of vegetable fiber reduces the risk of these diseases by reducing carbohydrate and lipid absorption [9,10,11]. Because vegetables also contain potassium, which improves hypertension [12,13], vegetable intake may help prevent metabolic syndrome-related diseases. Low-density lipoprotein (LDL) oxidation via reactive oxygen species is one of the causes of atherosclerotic illnesses [14], and vegetables are rich in antioxidant components such as polyphenols and vitamin C [15]. A reduced risk of bone fractures [16,17] and improved cognitive function [18,19,20] have been reported to be associated with vegetable and fruit consumption. In Japan, factors contributing to the need for nursing care include metabolic syndrome, frailty, and dementia [21]. The difference between healthy and average life expectancies is ~10 years in many Asian countries, meaning that long-term care is necessary for that duration [22]. One of the reasons for this difference is low vegetable intake. Such intake is expected to contribute to an increase in healthy life expectancy.
Although vegetables promote health, they are difficult to eat due to their flavor and physical properties and often require preparation to be palatable [23]. However, depending on the cooking method, the nutrients they contain may be reduced. For example, vitamin C in carrots decreases during heating (Figure 2) [24].
Salads are a simple and delicious way to consume vegetable nutrients by pouring mayonnaise, dressing, olive oil, or other seasonings over vegetables [25]. In this review article, we summarized the health benefits of consuming vegetable salads, especially those that can contribute to improving outcomes regarding lifestyle-related disease and enhance the absorption of the nutrients in vegetables.

2. Improvement in Body Weight and Serum Cholesterol Concentration Through Vegetable Salad Consumption

Health problems associated with poor dietary habits, such as obesity, metabolic syndrome, diabetes, hypertension, stroke, and coronary heart disease, are becoming more serious. The dietary fiber intake among Indonesian people is 10 g, which is quite low [26]. A lack of fiber is a risk factor for metabolic syndrome [27]. This study considered the possibility that this is due to inadequate fiber intake (i.e., insufficient vegetable intake). A previous study examined the effects of consuming 400 g of vegetables daily [26]. The study was a parallel group comparison trial in which 60 postmenopausal Indonesian women were randomly paired into two groups (vegetable and control groups). Subjects consumed 400 g of vegetables and 20 g/200 g vegetables with mayonnaise, roasted sesame dressing, traditional peanut sauce, or chili sauce daily for 21 days. We served 400 g of vegetables daily in a salad that varied from day to day. Daily variations included three of the following vegetables: carrot, green beans, cucumber, corn, cauliflower, tomato, lettuce, cabbage, pumpkin, beansprouts, mustard greens, Chinese cabbage, broccoli, squash, and chayote. The results showed significant reductions in the total cholesterol (TC), LDL cholesterol, high-density lipoprotein (HDL) cholesterol, body weight, and body mass index (BMI) in the vegetable group compared to the baseline (p < 0.05). After 21 days, there was a significant decrease in energy, lipid, and carbohydrate intake (p < 0.05) and a significant increase in vegetable and fiber intake (p < 0.05). The changes in the LDL cholesterol and body weight are shown in Figure 3 [26]. These results indicated that consuming a healthy diet that includes 400 g of vegetables daily may improve diet, weight management, and lipid profiles
The above study reported a decrease in the incidence of coronary artery disease as vegetable intake increased, as shown in Figure 1 [7], and the consumption of 300 g of vegetables per day was found to reduce the risk of coronary artery disease by 20% compared to no consumption, but the risk remained, even with a higher intake [7]. Increasing vegetable intake has been reported to improve metabolic syndrome in children, adults, and elderly persons [28,29,30,31].
A study on the relationship between vegetable intake and body weight reported an inverse correlation between vegetable intake and body weight [32].
Although the above study examined a salad intake of approximately 400 g/day, it suggests that using mayonnaise or dressing to increase vegetable intake may be effective in preventing metabolic syndrome.

3. Inhibition of Postprandial Blood Sugar (PPBS) Levels Increases by Consuming Vegetable Salad Before Rice

Consuming vegetable salad before carbohydrates moderates the fluctuation of PPBS concentrations and is the so-called “vegetable-first” effect [33,34,35]. Considering that the effect of eating vegetables first is the effect of dietary fiber, this study also evaluated the effect of vegetable salad extract (i.e., with solids removed) consumed before carbohydrates on PPBS concentrations [36].
A single intake crossover method was used for 13 healthy males aged >20 (washout of 1 week). The subjects had their blood sampled while hungry after an overnight fast and were asked to consume meals in three different orders: rice–vegetable salad, vegetable salad–rice, and vegetable salad extract–rice. The subjects were fed 150 g of rice, 175 g of cabbage-based vegetable salad, and 45 g of roasted sesame dressing. Blood samples were taken 30, 45, 60, 90, and 120 min after the consumption of the test diet to measure serum glucose and insulin concentrations (Figure 4). The serum glucose concentrations were significantly lower in vegetable salad–rice than rice–vegetable salad at 45 and 60 min. No significant differences were found between vegetable salad extract–rice and vegetable salad–rice or rice–vegetable salad. The serum insulin levels were significantly lower in vegetable salad–rice than rice–vegetable salad at 90 min. No significant differences were found between vegetable salad extract–rice and vegetable salad–rice or rice–vegetable salad. The results indicated that the consumption of vegetable salad before rice suppresses the increase in serum glucose concentration. The vegetable-first effect could not be explained solely by the effect of dietary fiber, as the vegetable salad extract reduced increases in blood glucose and insulin levels, although the effect was weak. As a consideration, in addition to the effect of dietary fiber, the effects of polyphenols, dressing (oil and vinegar), and chewing may have combined to suppress the increase in blood glucose levels [37,38,39].
In a recent report, it was shown that consuming potato salad before a rice meal suppresses the increase in PPBS levels [40]. The effect of cooking and cooling on the potato salad increased the amount of resistant starch, confirming that potato salad suppresses the increase in PPBS levels compared to steamed potatoes [41].

4. Increased Vegetable Intake and Improved Diabetes Indicators with Mayonnaise and Dressing Use

In Vietnam, an important factor in type 2 diabetes is not obesity but rather low vegetable and fiber intake [42,43,44,45]. Dietary fiber helps control blood glucose levels and can be used in the diets of people with diabetes. Vegetables are the main source of fiber in Vietnamese cuisine, but their intake is very low. This study attempted to increase vegetable and fiber intake with dressings and mayonnaise and evaluated their effects on glucose metabolism [46]. Sixty people with type 2 diabetes were randomly divided into intervention and control groups by creating 30 pairs according to their gender, age, BMI, and years of type 2 diabetes. Both groups received basic nutrition education on vegetables. The intervention group was further instructed to use roasted sesame dressing and egg yolk-type mayonnaise (the usage of the mayonnaise and dressing was not known, as the subjects were allowed to consume freely).
The study period was 2 weeks. The control and intervention groups had 300 and 450 g vegetable intake, respectively. At the end of the study, blood fructosamine levels in the intervention group were significantly lower than before the intake (p < 0.05) but not in the control group (p > 0.05).
Although this study did not specify the type of vegetables consumed, the fiber intake was about 8 g in the control group and 12 g in the intervention group [46]. Some agents found in GLV may cause a decrease in the incidence of cardiovascular diseases (CVDs). The first meta-analysis study focusing solely on GLVs (cruciferous vegetables such as cauliflower, cabbage, cress, bok choy, broccoli, kale, collard greens, and similar GLVs and their roots) found that high daily GLV intake significantly reduces the incidence of several CVDs [47]. GLV consumption decreases bile acid recirculation, utilizing cholesterol to synthesize bile acids, reducing fat absorption, and ultimately decreasing the risk of heart diseases [48]. GLVs also contain nitrates that, when consumed regularly, produce sufficient blood and tissue levels of nitrite and nitric oxide groups to compensate for disturbances in endogenous nitric oxide synthesis [49]. GLVs are also high in magnesium, which can lower the risk of CVD [50]. Molecular studies have shown that trace elements and some antioxidants in GLVs lower the risk of cancer through mechanisms that modulate free radical attack on nucleic acids, proteins, and polyunsaturated fatty acids [51].

5. Mayonnaise Promotes Carotenoid Absorption

Carotenoids in carrot and broccoli are difficult to absorb without modification [52,53]. Because mayonnaise is often consumed with vegetables, studies have been conducted on mayonnaise consumption and vegetable nutrient absorption. Egg yolk-type mayonnaise and broccoli (boiled) together enhance lutein and zeaxanthin absorption compared to broccoli consumed on its own [52]. Egg yolk-type mayonnaise and edible vegetable oils and lipids used in mayonnaise increase postprandial serum β-carotene concentrations compared to carrots consumed alone (Figure 5) [53]. It is thought that β-carotene cannot be synthesized in the human body [54], so β-carotene levels in the blood are derived from dietary sources, indicating that mayonnaise enhances carotenoid absorption.
Regarding the absorption-enhancing effect of mayonnaise consumption on carotenoids, in vitro studies have shown that mayonnaise enhances β-carotene dissolution into the oil layer compared to oil alone in the gastric model. This is due to the emulsifying effect of egg yolk (especially egg yolk lecithin) in mayonnaise [55], and sweet mayonnaise with added sugar enhances β-carotene absorption from fruits [56]. When moderately hypercholesterolemic Japanese men ate one chicken egg daily, their serum lutein and zeaxanthin concentrations increased and LDL oxidation was inhibited [57].
Considering the above, as the carotenoid absorption enhancement effect of egg yolk-type mayonnaise is due to the effect of egg yolk and vegetable oil, carotenoid absorption is greater with mayonnaise than with vegetable oil [55]. It has also been surmised that this effect could be obtained with other types of mayonnaise, such as the whole-egg type.

6. Calcium Absorption Enhancement Using Mayonnaise

Although vegetables contain a large amount of calcium, it is not well absorbed due to oxalic acid, which inhibits calcium absorption and other factors present in vegetables [58,59,60,61]. It has been reported that, after dairy products, the second largest source of calcium intake among Japanese people is vegetables [4]. Spinach, in particular, is known to be high in oxalic acid [62].
Because mayonnaise is an acidic food that contains vinegar, the calcium in the vegetables dissolves into acetic acid and increases absorption [62]. Therefore, this study evaluated the effect of mayonnaise on calcium absorption in rats. This calcium absorption-enhancing effect was higher than that of acetic acid [63].
The vinegar contained in mayonnaise influences the calcium absorption-promoting effect of mayonnaise. Acetic acid, the main ingredient in vinegar, can dissolve calcium. However, because mayonnaise enhances calcium absorption more than vinegar, it is assumed that it contains ingredients other than vinegar that enhance calcium absorption. The active ingredients in mayonnaise are not clear and will be the subject of future studies.

7. Effect of Serum Cholesterol Concentrations of Mayonnaise Consumption

Mayonnaise is made from vegetable oils, egg yolk, and acetic acid. In Japan, its ingredients are strictly regulated by the Japanese Agricultural Standards [64]. Dressings and creamy salad dressings are generally referred to as “mayonnaise-type” products [64]. Mayonnaise is mainly affected by edible vegetable oil because of its high vegetable oil content. Edible vegetable oils commonly used in mayonnaise are soybean or rapeseed oil, which contain high amounts of oleic and linoleic acids [24]. Because these oleic and linoleic acids lower serum cholesterol levels [65], it is possible that mayonnaise could also lower serum cholesterol. In contrast, the raw material contains egg yolks. The recommended daily intake of 15 to 20 g of egg yolk-type mayonnaise contains 22.5 to 30 mg of cholesterol [24,52]. The effects of mayonnaise consumption on serum cholesterol in healthy subjects or dyslipidemic patients are summarized in Table 1. This shows that the intervention with mayonnaise that contains egg yolk and soybean oil could decrease TC and LDL cholesterol levels. Soybean oil is an emulsifier used in mayonnaise to increase its viscosity and stability [66].
In healthy subjects, consuming 15 g of egg yolk-type mayonnaise (rapeseed oil-based) daily for 12 weeks did not affect serum TC or LDL cholesterol concentrations [67]. A 70-day study of healthy Chinese youths who ate 15 g of egg yolk-type mayonnaise (soybean oil) daily resulted in a significant increase in serum TC concentrations compared to the baseline, but only by 2.9%. It did not affect LDL cholesterol concentrations [68]. Since seasonal variations in serum total cholesterol concentrations have been reported to be 3.9 mg/dL in men [69], we consider this to be a non-problematic increase [69]. In hypercholesterolemic subjects, consuming 15 g of egg yolk-type mayonnaise (rapeseed oil-based) daily for 12 weeks significantly reduced serum TC and LDL cholesterol concentrations compared to the baseline [70]. When Malaysian hypercholesterolemia subjects were given palm or soybean oil-based egg yolk-type mayonnaise in a 4-week crossover study, palm and soybean oil-based mayonnaise lowered serum TC and LDL cholesterol concentrations. The degree of decline was greater for soybean oil-based mayonnaise [71]. In a study in which hypercholesterolemic subjects consumed whole-egg mayonnaise (as a control group for a phytosterol ester-containing mayonnaise-type study), total serum cholesterol and LDL cholesterol concentrations were not affected [72]. It is unclear why whole-egg mayonnaise did not lower serum TC and LDL cholesterol concentrations. Egg white protein lowers serum cholesterol concentrations. However, because the effect can be expected with at least ~8 g of egg white protein ingested daily [73], the effect cannot be expected by the small amount contained in mayonnaise. Cholesterol-lowering effects have also been reported for egg yolk lecithin, but the amount in mayonnaise is so small that it has been thought to have no effect [74,75]. The effect of mayonnaise on serum cholesterol concentrations is the result of edible vegetable oil, but the study did not appear to show any effect of edible vegetable oil. However, the details of the type of edible vegetable oil are unknown because it is not mentioned in the study [72]. Based on the above, 15 to 20 g of mayonnaise daily does not affect serum TC and LDL cholesterol concentrations in healthy and dyslipidemic subjects and can be safely consumed.
In recent years, there have been mayonnaise-type dressings that do not use eggs [66,76,77,78,79], mayonnaise made with egg yolks from which cholesterol has been removed with supercritical CO2 fluid [80], and mayonnaise-type dressings containing plant sterols that lower blood cholesterol levels [81,82,83]. For those concerned about the energy content of mayonnaise, low-energy mayonnaise-type dressings are available [84,85]; for those concerned about blood pressure, mayonnaise made with flaxseed oil, rich in α-linolenic acid, which lowers blood pressure, is also available [86,87].
Table 1. The effects of mayonnaise consumption on serum cholesterol in healthy subjects or dyslipidemic patients.
Table 1. The effects of mayonnaise consumption on serum cholesterol in healthy subjects or dyslipidemic patients.
StudySubjectsTest MayonnaiseDesignDurationMain Outcome
(% vs. Before Intake)
Reference
Tohgi N et al.
(1997)
Healthy (n = 9)Egg yolk type
Canola oil base
15 g/day
Open trial12 weeksTC: No change
LDL-C: No change
[67]
Xu WB et al.
(2012)
Healthy (n = 47)Egg yolk type
Soybean oil base
15 g/day
Open trial70 daysTC: 2.9%
LDL-C: No change
[68]
Matsuoka R et al.
(2001)
Mildly hypercholesterolemic
(n = 10)
Egg yolk type
Canola oil base
15 g/day
Open trial12 weeksTC: −6.3%
LDL-C: −8.4%
[70]
Karupaiah T et al.
(2016)
Normal and mildly hypercholesterolemic
(n = 34)
Egg yolk type
Soybean oil or
palm oil
20 g/day
Cross-over4 weeksPalm oil base:
TC: −2.7%
LDL-C: −4.5%
Soybean oil base:
TC: −7.7%
LDL-C: −9.5%
[71]
Ishizaki T et al.
(2003)
Normal and mildly hypercholesterolemic
(n = 29)
Whole-egg type
Oil unknown
15 g/day
RCT3 monthsTC: No change
LDL-C: No change
[72]
TC: total cholesterol; LDL-C: LDL cholesterol; RCT: randomized controlled study.

8. Discussion

This review showed that vegetable salad increases vegetable intake, improves lipid and glucose metabolism, and enhances carotenoid and calcium absorption from vegetables.
Fruit and vegetable consumption is associated with decreased all-cause mortality and reduced cancer and cardiovascular mortality. Vegetables may have a stronger association with mortality than fruits [88].
In terms of preventing cardiovascular mortality, the effects of vegetable salad consumption on weight loss and metabolic syndrome prevention appear to be due to dietary fiber. As dietary fiber remains in the stomach longer [89], vegetable consumption is expected to make people feel full and reduce the intake of meals high in carbohydrates and lipids. Dietary fiber suppresses carbohydrate and lipid absorption. There are also benefits of chewing and consuming vegetables. Regarding the effect of mastication, cabbage consumption increases the number of times one has to chew compared to rice, boiled eggs, fish, and sausages [90]. The more chewing is performed, the more saliva is secreted [91]. Vegetable dietary fiber can hold water; when mixed with saliva through chewing, it becomes gelatinous and viscous [92]. The high viscosity of gastric contents slows carbohydrate absorption [93]. Epidemiological studies that examined the relationship between chewing ability and diabetes reported that groups with a strong chewing ability had a reduced risk of diabetes compared to groups with a weak chewing ability [94]. More frequent chewing increases insulin secretion and suppresses increases in PPBS concentrations [95]. The consumption of olive oil and rice together suppresses increases in PPBS concentrations in a concentration-dependent manner, although the difference is insignificant [38].
In terms of cancer, a study in Italy showed that the dietary pattern of salad vegetables had a protective effect against HER (human epidermal growth factor receptor)-2-positive cancers, much stronger than HER-2-negative cancers [96]. An important finding is that the dietary pattern of salad vegetables protects mainly against a specific breast cancer subtype [96]. A study in the United States showed that soluble CD44 (cluster of differentiation 44), a simple and inexpensive marker of cancer stem cells, increased in oral cancer patients who ate more green salad [97]. This was the first study to show that increased green salad intake is associated with improved progression-free and overall survival and lower CD44 levels in mouthwash from oral cancer cases with long-term follow-ups. Eating salad is one way for patients to increase vegetable consumption to prolong their survival [97]. Furthermore, dietary fiber reduces the risk of gastric, colorectal, and breast cancers, suggesting that vegetable consumption may help prevent cancer [98,99,100,101,102]. In addition, vegetables have been reported to contain many other bioactive substances and nutrients. Dietary fiber, abundant in vegetables, improves bowel movements, and the same effect can be seen in the consumption of vegetable salads [103,104]. Dietary fiber is known to improve the intestinal environment [105]. It has been reported that dietary fiber improves the intestinal environment, upgrades the colonic mucus barrier, and enhances immune function, thereby reducing susceptibility to pathogens [106,107]. In addition, antioxidant components such as polyphenols and carotenoids, which are included in vegetables, have also been reported to improve the intestinal environment [108,109]. Rocket salad also contains lactic acid bacteria, which have been reported to improve the intestinal environment [110,111]. However, the effect of vegetable salad consumption on improving the intestinal environment has not been reported; therefore, we will expect this to be investigated in future studies.
Vegetables contain a lot of antioxidant components such as carotenoids, vitamin C, vitamin E, and polyphenols (flavonoids, etc.) [24,112]. It has also been reported that salad seasonings such as herbs and vinegar have antioxidant capacities [112]. In this review, we have shown that mayonnaise promotes carotenoid absorption from carrots and broccoli [52,53]. For this reason, it is considered that antioxidant activity in humans is also caused by the ingestion of antioxidants as a salad. It has also been reported that a high intake of vegetables reduces oxidative stress in humans [113]. Because oxidation in vivo has become a risk factor for arteriosclerotic diseases, cancer, and Alzheimer’s disease [14,114,115], salad is considered to have the potential to prevent these diseases.
Vegetables also contain many other nutrients. In Japan, numerous foods with function claims that are ingredients contained in vegetables and used as active ingredients have been submitted and accepted [116]. Table 2 summarizes the ingredients related to vegetables extracted from the search results for “fresh foods” on the foods with function claims search site [116]. Since functional foods in Japan can be submitted with evidence of active components, it is necessary to confirm the effects of vegetables per se in the future, since RCTs are often not conducted on the vegetables themselves. Furthermore, a subject for future study would involve determining how the function of such vegetable components is altered when incorporated into a salad.
In an American study, subjects who ate salads had a better intake of dietary fiber, total fat, unsaturated fatty acids, vitamins A, B6, C, E, and K, folate, choline, magnesium, potassium, and sodium [117]. The number of subjects was significantly higher for the total food ingredients of vegetables, green vegetables, nuts, whole fruits, total protein foods, seafood, vegetable proteins, fatty acids, refined grains, and added sugars [117]. The consumption of salads, raw vegetables, and salad dressings was positively associated with increased levels of the following serum micronutrients: folic acid, vitamins C and E, lycopene, and α- and β-carotene. Each serving of salad had a vitamin C content of >100% of the dietary recommendations [118].
Overall, vegetable salad products can be an alternative healthy food [119]. Based on the above, although salad is a food that contains diverse ingredients, the dietary fiber in vegetables and the vinegar and edible vegetable oils and lipids contained in mayonnaise and dressings contribute mainly to health functions.
The results of a study conducted on Indonesian students showed that vegetable salad is well received in terms of taste, aroma, and presentation [119]. Although vegetable intake is recommended in many countries, it is likely that the intake does not meet the recommended amounts in many cases. Although vegetables contain components involved in health promotion, it is assumed that their intake may be avoided due to the complexity of their preparation and their flavor [120].
Salads are easy to prepare and a tasty way to consume vegetables. However, there may be cases where raw vegetables cannot be consumed for safety reasons. In this case, using mayonnaise or dressing on warm vegetables can also be a tasty and healthy way to consume vegetables.
Vegetable intake alone does not provide protein, but adding eggs, cheese, or chicken to a vegetable salad does. Eggs contain many nutrients but not vitamin C and fiber, and they are thought to provide a balanced diet when consumed with salad. In contrast, because mayonnaise and dressings use edible vegetable oils and lipids as ingredients, there is an apprehension that their excessive consumption may lead to a high energy intake, so they must be used in moderation.

9. Conclusions

This review focuses on the functions that vegetable salads serve in terms of health, particularly those consumed with mayonnaise or dressing. It has been reported that vegetable salads function in two ways: first, increased vegetable intake is effective in terms of helping to prevent lifestyle-related diseases by improving glucose metabolism, obesity, and lipid metabolism; second, salad seasonings are effective in promoting the absorption of the carotenoids and calcium contained in vegetables.
Future research into the health functions of these functional vegetable ingredients would further enhance the health value of vegetables and vegetable salads. This review will contribute to the maintenance and improvement of health through the intake of salads.

Author Contributions

Conceptualization, D.M.U. and R.M.; writing—original draft preparation, D.M.U., I.K.-S., T.M., H.U., Y.T., M.O., W.W., R.M., S.K. and M.S.; writing—review and editing, D.M.U. and S.Y.; supervision, S.Y. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

No new data were created or analyzed in this study.

Acknowledgments

We thank Kazunori Utsunomiya for providing technical advice on this experiment.

Conflicts of Interest

D.M.U., I.K.-S., S.K., M.S. and S.Y. declare no conflicts of interest. T.M., H.U., Y.T., M.O., W.W. and R.M. are employees of Kewpie Corporation. There are no other patents, products in development, or marketed products to declare. Kewpie Corporation and PT Kewpie Indonesia have no conflicts of interest with this research.

Abbreviations

BMIbody mass index
CDcluster of differentiation
CVDcardiovascular disease
GLVgreen leaf vegetable
HDLhigh-density lipoprotein
HERhuman epidermal growth factor
IAUCincremental area under the curve
LDLlow-density lipoprotein
PPBSpostprandial blood sugar
RCTrandomized controlled study
SEMstandard error of the mean
TCtotal cholesterol

References

  1. Slavin, J.L.; Lloyd, B. Health benefit of fruit and vegetable. Adv. Nutr. 2012, 3, 506–516. [Google Scholar] [CrossRef] [PubMed]
  2. Ford, E.S.; Bergmann, M.M.; Boeing, H.; Capewell, S. Healthy lifestyle behaviors and all-cause mortality among adults in the United States. Prev. Med. 2012, 55, 23–27. [Google Scholar] [CrossRef] [PubMed]
  3. Health Japan 21 Analysis and Assessment Project, National Institute of Health and Nutrition, Health Japan 21 (the Second Term). Available online: https://www.nibiohn.go.jp/eiken/kenkounippon21/en/kenkounippon21/ (accessed on 10 October 2024).
  4. National Institute of Health and Nutrition, The National Health and Nutrition Survey (NHNS) Japan, 2019 Summary. Available online: https://www.nibiohn.go.jp/eiken/kenkounippon21/download_files/eiyouchousa/2019.pdf (accessed on 10 October 2024).
  5. IPB University Report, Indonesia Vegetable Intake Study, Executive Summary. Available online: http://njppp.jp/wp/wp-content/uploads/ec28b2b7666cb3d52c198d75646311bd.pdf (accessed on 10 October 2024).
  6. Indonesia Health Survey 2023, Ministry of Health Republic of Indonesia. Available online: https://www.kemkes.go.id/id/survei-kesehatan-indonesia-ski-2023 (accessed on 10 October 2024). (In Indonesian).
  7. Aune, D.; Giovannucci, E.; Boffetta, P.; Fadnes, L.T.; Keum, N.; Norat, T.; Greenwood, D.C.; Riboli, E.; Vatten, L.J.; Tonstad, S. Fruit and vegetable intake and the risk of cardiovascular disease, total cancer, and all-cause mortality—A systematic review and dose-response meta-analysis of prospective studies. Int. J. Epidemiol. 2017, 46, 1029–1056. [Google Scholar] [CrossRef] [PubMed]
  8. Alemany, M. The metabolic syndrome, a human disease. Int. J. Mol. Sci. 2024, 25, 2251. [Google Scholar] [CrossRef] [PubMed]
  9. Shirouchi, B.; Kawamura, S.; Matsuoka, R.; Baba, S.; Nagata, K.; Shiratake, S.; Tomoyori, H.; Imaizumi, K.; Sato, M. Dietary guar gum reduces lymph flow and diminishes lipid transport in thoracic duct-cannulated rats. Lipids 2011, 56, 789–793. [Google Scholar] [CrossRef]
  10. Wei, B.; Liu, Y.; Lin, X.; Fang, Y.; Cui, J.; Wan, J. Dietary fiber intake and risk of metabolic syndrome. Clin. Nutr. 2018, 37, 1935–1942. [Google Scholar] [CrossRef]
  11. Chen, J.P.; Chen, G.C.; Wang, X.P.; Qin, L.; Bai, Y. Dietary fiber and metabolic syndrome: Meta-analysis and review of related mechanisms. Nutrients 2017, 10, 24. [Google Scholar] [CrossRef]
  12. McLean, R.M.; Wang, N.X. Potassium. Adv. Food Nutr. Res. 2021, 96, 89–121. [Google Scholar]
  13. Fillippini, T.; Naska, A.; Kasdagli, M.I.; Torres, D.; Lopes, C.; Carvalho, C.; Moreira, P.; Malavolti, M.; Orsini, N.; Whelton, P.K.; et al. Potassium intake and blood pressure: Dose response meta-analysis of randomized controlled trials. J. Am. Heart Assoc. 2020, 9, e015719. [Google Scholar] [CrossRef]
  14. Steinberg, D.; Parthasarathy, S.; Carew, T.E.; Khoo, J.C.; Witztum, J.L. Beyond cholesterol. Modifications of low-density lipoprotein that increase its atherogenicity. N. Engl. J. Med. 1989, 320, 915–924. [Google Scholar]
  15. Kosewski, G.; Kowalówka, M.; Drzymała-Czyż, S.; Przysławski, J. The impact of culinary processing, including sous-vide, on polyphenols, vitamin C content and antioxidant status in selected vegetables—Methods and results: A critical review. Foods 2023, 12, 2121. [Google Scholar] [CrossRef] [PubMed]
  16. Zeraattalab-Motlagh, S.; Ghoreishy, S.M.; Arab, A.; Mahmoodi, S.; Hemmati, A.; Mohammadi, H. Fruit and vegetable consumption and the risk of bone fracture: A Grading of Recommendations, Assessment, Development, Evaluations (GRADE)-assessed systematic review and dose-response meta-analysis. JBMR Plus 2023, 7, e10840. [Google Scholar] [CrossRef] [PubMed]
  17. Rizzoli, R.; Biver, E.; Brennan-Speranza, T.C. Nutritional intake and bone health. Lancet Diabetes Endocrinol. 2021, 9, 606–621. [Google Scholar] [CrossRef] [PubMed]
  18. Carrillo, J.Á.; Zafrilla, M.P.; Marhuenda, J. Cognitive function and consumption of fruit and vegetable polyphenols in a young population: Is there a relationship? Foods 2019, 8, 507. [Google Scholar] [CrossRef]
  19. F Fangfang, H.; Qiong, W.; Shuai, Z.; Xiao, H.; Jingya, Z.; Guodong, S.; Yan, Z. Vegetable and fruit intake, its patterns, and cognitive function: Cross-sectional findings among older adults in Anhui. China. Nutr. Health Aging 2022, 26, 529–536. [Google Scholar] [CrossRef]
  20. Huang, L.; Zhao, C.; Gao, M.; Tao, Y.; Chen, X.; Chen, H.; Li, F.; Zheng, Y.; Lu, M.; Ma, Y.; et al. Associations of vegetable and fruit with cognitive function and its decline: Two longitudinal studies. J. Nutr. Health Aging 2024, 28, 100223. [Google Scholar] [CrossRef]
  21. Ministry of Health, Labour and Welfare, Government of Japan, Summary Report of Comprehensive Survey of Living Conditions 2019. Available online: https://www.mhlw.go.jp/english/database/db-hss/dl/report_gaikyo_2019.pdf (accessed on 10 October 2024).
  22. World Health Organization. Life Expectancy and Healthy Life Expectancy, Data by Country. Available online: https://apps.who.int/gho/data/view.main.SDG2016LEXv?lang=en (accessed on 10 October 2024).
  23. Kumagai, K.; Kuramori, M. Effects of Dietary Habits and Parents’ Awareness of Dietary Life on Vegetable Intake of Elementary School Children. Jpn. J. Nutr. Diet. 1996, 54, 251–258. (In Japanese) [Google Scholar]
  24. Ministry of Education, Culture, Sports, Science and Technology, Government of Japan, Standard Tables of Food Composition in Japan 2015 (7th Revised Version). Available online: https://www.mext.go.jp/en/policy/science_technology/policy/title01/detail01/1374030.htm (accessed on 10 October 2024).
  25. Nishida, T. A well-balanced diet that enhances QOL and the role of salads and salad dressing. J. Integr. Study Diet. Habits 2022, 33, 72–78. (In Japansese) [Google Scholar] [CrossRef]
  26. Kartiko Sari, I.; Utari, D.M.; Kamoshita, S.; Oktaviana, D.; Sakai, S.; Nishiyama, H.; Masuda, Y.; Yamamoto, S. Increasing vegetable intake 400 g/day to control body weight and lipid profile in overweight hyperlipidemia menopausal women. J. Public Health Res. 2020, 9, 1733. [Google Scholar] [CrossRef]
  27. Veluvali, A.; Snyder, M. Dietary fiber deficiency in individuals with metabolic syndrome: A review. Curr. Opin. Clin. Nutr. Metab. Care 2023, 26, 564–569. [Google Scholar] [CrossRef]
  28. Hosseinpour-Niazi, S.; Bakhshi, B.; Betru, E.; Mirmiran, P.; Darand, M.; Azizi, F. Prospective study of total and various types of vegetables and the risk of metabolic syndrome among children and adolescents. World J. Diabetes 2019, 10, 362–375. [Google Scholar] [CrossRef] [PubMed]
  29. Papaioannou, K.G.; Kadi, F.; Nilsson, A. Benefits of Fruit and Vegetable Consumption on Prevalence of Metabolic Syndrome Are Independent of Physical Activity Behaviors in Older Adults. Nutrients 2022, 14, 263. [Google Scholar] [CrossRef] [PubMed]
  30. Matsumoto, M.; Suganuma, H.; Shimizu, S.; Hayashi, H.; Sawada, K.; Tokuda, I.; Ihara, K.; Nakaji, S. Skin Carotenoid Level as an Alternative Marker of Serum Total Carotenoid Concentration and Vegetable Intake Correlates with Biomarkers of Circulatory Diseases and Metabolic Syndrome. Nutrients 2020, 12, 1825. [Google Scholar] [CrossRef] [PubMed]
  31. Lim, M.; Kim, J. Association between fruit and vegetable consumption and risk of metabolic syndrome determined using the Korean Genome and Epidemiology Study (KoGES). Eur. J. Nutr. 2020, 59, 1667–1678. [Google Scholar] [CrossRef]
  32. Nour, M.; Lutze, S.A.; Grech, A.; Allman-Farinelli, M. The Relationship between Vegetable Intake and Weight Outcomes: A Systematic Review of Cohort Studies. Nutrients 2018, 10, 1626. [Google Scholar] [CrossRef]
  33. Maruyama, C.; Kikuchi, N.; Masuya, Y.; Hirota, S.; Araki, R.; Maruyama, T. Effects of green-leafy vegetable intake on postprandial glycemic and lipidemic responses and α-tocopherol concentration in normal weight and obese men. J. Nutr. Sci. Vitaminol. 2013, 59, 264–271. [Google Scholar] [CrossRef]
  34. Imai, S.; Fukui, M.; Kajiyama, S. Effect of eating vegetables before carbohydrates on glucose excursions in patients with type 2 diabetes. J. Clin. Biochem. Nutr. 2014, 54, 7–11. [Google Scholar] [CrossRef]
  35. Kanamoto, I.; Inoue, Y.; Moriuchi, T.; Yamada, Y.; Imura, H.; Sato, S. Effect of differences in low Glycemic Index Food Intake Sequence on Plasma Glucose Profile. J. Jpn. Diab. Soc. 2010, 53, 96–101. (In Japanese) [Google Scholar]
  36. Tanaka, T.; Sakamoto, H.; Matsuoka, R.; Utsunomiya, K. Ingestion of vegetable salads before rice inhibits the increase in postprandial serum glucose levels in healthy subjects. Biosci. Biotech. Biochem. 2023, 87, 1212–1218. [Google Scholar] [CrossRef]
  37. Kim, Y.; Keogh, J.B.; Clifton, P.M. Polyphenols and glycemic control. Nutrients 2016, 8, 17. [Google Scholar] [CrossRef]
  38. Uenaka, S.; Yagi, M.; Takabe, W.; Yonei, Y. The effects of food materials on postprandial hyperglycemia. Glycative Stress. Res. 2020, 7, 220–231. [Google Scholar]
  39. Endo, M.; Matsuoka, T. The efficacy of vinegar on the suppression of postprandial glucose elevation. J. Jpn. Diab. Soc. 2011, 54, 192–199. (In Japanese) [Google Scholar]
  40. Kamijo, F.; Yoshimura, Y.; Takeda, Y.; Matsuoka, R.; Utsunomiya, K. Effects of the order of intake of potato salad and rice on postprandial blood glucose level in Japanese subjects. In Proceedings of the 70th Annual Meeting of Japanese Society of Nutrition and Dietetics, Nagoya, Japan, 1–3 September 2023. [Google Scholar]
  41. Yoshimura, Y.; Yoshida, Y.; Kamijo, F.; Takeda, Y.; Matsuoka, R.; Utsunomiya, K. Mixing potatoes with mayonnaise and cooling them suppresses postprandial blood glucose level in Japanese subjects. In Proceedings of the 70th Anniversary Annual Meeting of The Japanese Society for Food Science and Technology, Kyoto, Japan, 24–26 August 2023. [Google Scholar]
  42. Yamamoto, S.; Le, D.S.N.T.; Hsu, T.F.; Huang, K.C.; Nguyen, V.H.; Wong, Y.; Huang, P.C. Vietnamese may develop type 2 diabetes with smaller increases in body mass index and waist circumference than Taiwanese. Int. J. Diabetol. Vasc. Dis. Res. 2013, 1, 1–5. [Google Scholar]
  43. Duc Son, L.N.T.; Hanh, T.T.M.; Kusama, K.; Kunii, D.; Sakai, T.; Hung, N.T.K.; Yamamoto, S. Anthropometric characteristics, dietary patterns and risk of type 2 diabetes mellitus in Vietnam. J. Am. Coll. Nutr. 2005, 24, 229–234. [Google Scholar] [CrossRef]
  44. Le Nguyen, T.D.; Tran, T.M.; Kusama, K.; Ichikawa, Y.; Nguyen, T.K.; Yamamoto, S. Vietnamese type 2 diabetic subjects with normal BMI but high body fat. Diabetes Care 2003, 26, 1941–1947. [Google Scholar]
  45. Quang, B.T.; Phuong Pham Tran, P.P.; Thanh, C.N.; Thi, N.B.; Dinh, T.D.; Quang, T.T.; Tuan, L.D.; Thuy, N.B.T.; Anh, N.N. High incidence of type 2 diabetes in a population with normal range body mass index and individual prediction nomogram in Vietnam. Diabet. Med. 2022, 39, e14680. [Google Scholar] [CrossRef]
  46. Thao, T.P.; Linh, N.T.; Nishiyama, H.; Sakai, S.; Shimura, F.; Yamamoto, S. Higher vegetable intake improved blood glucose level in Vietnamese with type 2 diabetes mellitus. Int. J. Clin. Nutr. Diet. 2017, 3, 124. [Google Scholar] [CrossRef]
  47. P Pollock, R.L. The effect of green leafy and cruciferous vegetable intake on the incidence of cardiovascular disease: A meta-analysis. JRSM Cardiovasc. Dis. 2016, 5, 2048004016661435. [Google Scholar] [CrossRef]
  48. Kahlon, T.S.; Chiu, M.M.; Chapman, M.H. Steam cooking significantly improves in vitro bile acid binding of collard greens, kale, mustard greens, broccoli, green bell pepper, and cabbage. Nutr. Res. 2008, 6, 351–357. [Google Scholar] [CrossRef]
  49. Milkowski, A.; Garg, H.K.; Coughlin, J.R.; Bryan, N.S. Nutritional epidemiology in the context of nitric oxide biology: A risk-benefit evaluation for dietary nitrite and nitrate. Nitric Oxide 2010, 22, 110–119. [Google Scholar] [CrossRef]
  50. Yiqing, S.; Ford, E.S.; Manson, J.E.; Liu, S. Relations of magnesium intake with metabolic risk factors and risks of type 2 diabetes, hypertension, and cardiovascular disease: A critical appraisal. Curr. Nutr. Food Sci. 2005, 1, 231–243. [Google Scholar]
  51. Philpott, M.; Ferguson, L.R. Immunonutrition and cancer. Mutat. Res. 2004, 551, 29–44. [Google Scholar] [CrossRef] [PubMed]
  52. Takeda, S.; Masuda, Y.; Usuda, M.; Marushima, R.; Ueji, T.; Hasegawa, M.; Maruyama, C. Effects of mayonnaise on postprandial serum lutein/zeaxanthin and beta-carotene concentrations in humans. J. Nutr. Sci. Vitaminol. 2009, 55, 479–485. [Google Scholar] [CrossRef] [PubMed]
  53. Marushima, R.; Takeuchi, A.; Masuda, Y.; Kunou, M.; Hasegawa, M.; Maruyama, C. Effect of mayonnaise on promoting β-carotene absorption in healthy adults. In Proceedings of the 59th Annual Meeting of Japan Society of Nutrition and Food Science, Tokyo, Japan, 13–15 May 2005. [Google Scholar]
  54. Ferreira, Y.A.M.; Jamar, G.; Estadella, D.; Pisani, L.P. Role of carotenoids in adipose tissue through the AMPK-mediated pathway. Food Funct. 2023, 14, 3454–3462. [Google Scholar] [CrossRef]
  55. Takeda, S.; Kimura, M.; Marushima, R.; Takeuchi, A.; Takizawa, K.; Ogino, Y.; Masuda, Y.; Kunou, M.; Hasegawa, M.; Maruyama, C. Mayonnaise contributes to increasing postprandial serum β-carotene concentration through the emulsifying property of egg yolk in rats and humans. J. Nutr. Sci. Vitaminol. 2011, 57, 209–215. [Google Scholar] [CrossRef]
  56. Li, C.; Masuda, Y.; Usuda, M.; Kimura, M.; Wang, W.; Xu, W.; Xi, Y. Effects of sweet mayonnaise intake on β-carotene absorption in rats. Food Sci. 2015, 36, 188–192. (In Chinese) [Google Scholar]
  57. Kishimoto, Y.; Taguchi, C.; Saita, E.; Suzuki-Sugihara, N.; Nishiyama, H.; Wang, W.; Masuda, Y.; Kondo, K. Additional consumption of one egg per day increases serum lutein plus zeaxanthin concentration and lowers oxidized low-density lipoprotein in moderately hypercholesterolemic males. Food Res. Int. 2017, 99, 944–949. [Google Scholar] [CrossRef]
  58. Uenishi, K.; Ezawa, I.; Kajimoto, M.; Tsuchiya, F. Calcium Absorption from Milk, Fish (Pond Smelt, Sardine) and Vegetables (Komatsuna-green, Jew’s Marrow, Saltwort) in Japanese Young Women. J. Jap. Soc. Food Nutr. 1998, 51, 259–266. (In Japanese) [Google Scholar] [CrossRef]
  59. Heaney, R.P.; Weaver, C.M. Calcium absorption from kale. Am. J. Clin. Nutr. 1990, 51, 656–657. [Google Scholar] [CrossRef]
  60. Heaney, R.P.; Weaver, C.M.; Recker, R.R. Calcium absorbability from spinach. Am. J. Clin. Nutr. 1988, 47, 707–709. [Google Scholar] [CrossRef]
  61. Kelsay, J.L.; Behall, K.M.; Prather, E.S. Effect of fiber from fruits and vegetables on metabolic responses of human subjects, II. Calcium, magnesium, iron, and silicon balances. Am. J. Clin. Nutr. 1979, 32, 1876–1880. [Google Scholar] [CrossRef] [PubMed]
  62. Kikunaga, S.; Takahashi, M. Determination of Oxalic Acid in Vegetables by Isotachophoresis. J. Jap. Soc. Food Nutr. 1985, 38, 123–128. (In Japanese) [Google Scholar] [CrossRef]
  63. Ji, S.J.; Masuda, Y.; Kimura, M.; Wang, W.; Li, C.; Xi, Y. Effects of mayonnaise on calcium absorption in rats. J. Shand. Agric. Univ. 2019, 35, 959–963. (In Chinese) [Google Scholar]
  64. Kimura, T.; Tanaka, T.; Umezu, T.; Ariizumi, M. New technological development for functional mayonnaise. Jpn. J. Food Eng. 2011, 12, 113–115. (In Japanese) [Google Scholar] [CrossRef]
  65. Mattson, F.H.; Grundy, S.M. Comparison of effects of dietary saturated, monounsaturated, and polyunsaturated fatty acid on plasma lipids and lipoproteins in man. J. Lipid Res. 1985, 26, 194–202. [Google Scholar] [CrossRef]
  66. Zanjani, M.M.; Yousefi, M.; Ehsani, A. Challenges and approaches for production of a healthy and functional mayonnaise sauce. Food Sci. Nutr. 2019, 7, 2471–2484. [Google Scholar] [CrossRef]
  67. Tohgi, N.; Nonaka, K. Effect of mayonnaise intake on serum lipid and apolipoprotein profiles. J. New Remedies Clin. 1997, 46, 1279–1282. (In Japanese) [Google Scholar]
  68. Xu, W.B.; Masuda, Y.; Usuda, M.; Matsuoka, R.; Kimura, M.; Wu, J.H.; Chen, J.; Wang, X.W.; Xi, Y.C. Effect of mayonnaise intake on blood lipid profile in humans. Food Sci. 2012, 33, 301–304. (In Chinese) [Google Scholar]
  69. Ockene, I.S.; Chiriboga, D.E.; Stanek, E.J., 3rd; Harmatz, M.G.; Nicolosi, R.; Saperia, G.; Well, A.D.; Freedson, P.; Merriam, P.A.; Reed, G.; et al. Seasonal variation in serum cholesterol levels: Treatment implications and possible mechanisms. Arch. Intern. Med. 2004, 164, 863–870. [Google Scholar] [CrossRef]
  70. Matsuoka, R.; Masuda, Y.; Takamiya, M.; Kawamura, M.; Hirayama, S.; Inukai, S.; Hasegawa, M.; Tohgi, N. Effect of mayonnaise on serum lipid concentrations in hyperlipidemic subjects. J. Jpn. Soc. Clin. Nutr. 2001, 23, 21–25. (In Japanese) [Google Scholar]
  71. Karupaiah, T.; Chuah, K.A.; Chinna, K.; Matsuoka, R.; Masuda, Y.; Sundram, K.; Sugano, M. Comparison of soybean oil- and palm olein-based mayonnaise on the plasma lipid and lipoprotein profiles in human subjects: A double-blind randomized controlled trial with cross-over design. Lipids Health Dis. 2016, 15, 131. [Google Scholar] [CrossRef] [PubMed]
  72. Ishizaki, T.; Wakabayashi, M.; Tanimoto, H.; Shima, A.; Yabune, M.; Kajimoto, O.; Hiroshige, I. Effects of long-term intake of mayonnaise containing phytosterol ester on blood cholesterol concentration in Japanese with borderline or mild cholesterolemia. J. Clin. Biochem. Nutr. 2003, 33, 75–82. [Google Scholar] [CrossRef]
  73. Matsuoka, R.; Kamachi, K.; Usuda, M.; Masuda, Y.; Kunou, M.; Tanaka, A.; Utsunomiya, K. Minimal effective dose of lactic-fermented egg white on visceral fat in Japanese men: A double-blind parallel-armed pilot study. Lipids Health Dis. 2019, 18, 102. [Google Scholar] [CrossRef] [PubMed]
  74. Imaizumi, K.; Sakono, M.; Sugano, M.; Shigematsu, Y.; Hasegawa, M. Influence of saturated and polyunsaturated egg yolk phospholipids on hyperlipidemia in rats. Agric. Biol. Chem. 1989, 53, 2469–2474. [Google Scholar]
  75. Ikeda, I.; Matsuoka, R.; Hamada, T.; Mitsui, K.; Imabayashi, S.; Uchino, A.; Sato, M.; Kuwano, E.; Itamura, T.; Yamada, K.; et al. Cholesterol esterase accelerates intestinal cholesterol absorption. Biochim. Biophys. Acta 2001, 1571, 34–44. [Google Scholar] [CrossRef]
  76. Caporaso, N.; Genovese, A.; Burke, R.; Barry-Ryan, C.; Sacchi, R. Effect of olive mill wastewater phenolic extract, whey protein isolate and xanthan gum on the behavior of olive O/W emulsions using response surface methodology. Food Hydrocoll. 2016, 61, 66–76. [Google Scholar] [CrossRef]
  77. Rahmati, K.; Mazaheri Tehrani, M.; Daneshvar, K. Soy milk as an emulsifier in mayonnaise: Physico-chemical, stability and sensory evaluation. J. Food Sci. Technol. 2014, 51, 3341–3347. [Google Scholar] [CrossRef]
  78. Chetana, R.; Bhavana, K.P.; Babylatha, R.; Geetha, V.; Suresh Kumar, G. Studies on eggless mayonnaise from rice bran and sesame oils. J. Food Sci. Technol. 2019, 56, 3117–3125. [Google Scholar] [CrossRef]
  79. Karshenas, M.; Goli, M.; Zamindar, N. The effect of replacing egg yolk with sesame-peanut defatted meal milk on the physicochemical, colorimetry, and rheological properties of low-cholesterol mayonnaise. Food Sci. Nutr. 2018, 6, 824–833. [Google Scholar] [CrossRef]
  80. Froning, G.W.; Wehling, R.L.; Cuppett, S.L.; Pierce, M.M.; Niemann, L.; Siekman, D.K. Extraction of cholesterol and other lipids from dried egg yolk using supercritical carbon dioxide. J. Food Sci. 1990, 55, 95–98. [Google Scholar] [CrossRef]
  81. Matsuoka, R.; Masuda, Y.; Takeuchi, A.; Marushima, R.; Onuki, M. Minimal effective dose of plant sterol on serum cholesterol concentration in Japanese subjects and safety evaluation of plant sterol supplemented in mayonnaise. J. Oleo Sci. 2004, 53, 17–27. (In Japanese) [Google Scholar] [CrossRef]
  82. Matsuoka, R.; Masuda, Y.; Takeuchi, A.; Marushima, R.; Hasegawa, M.; Sakamoto, A.; Hirata, H.; Kajimoto, O.; Homma, Y. A double-blind, placebo-controlled study on the effects of mayonnaise containing free plant sterol on serum cholesterol concentration; safety evaluation for normocholesterolemic and mildly hypercholesterolemic Japanese subjects. J. Oleo Sci. 2004, 53, 79–88. (In Japanese) [Google Scholar] [CrossRef]
  83. Matsuoka, R. Property of phytosterols and development of its containing mayonnaise-type dressing. Foods 2022, 11, 1141. [Google Scholar] [CrossRef] [PubMed]
  84. Tohgi, N.; Koyama, K.; Kono, S.; Nonaka, K. Effect of low-calorie mayonnaise intake on serum lipid and apolipoprotein profiles. J. New Remedies Clin. 1997, 46, 921–924. (In Japanese) [Google Scholar]
  85. Tohgi, N.; Koyama, K.; Kono, S.; Nonaka, K. Effect of long-term intake of low-calorie mayonnaise on serum lipid and apolipoprotein profiles. J. New Remedies Clin. 1997, 46, 540–573. (In Japanese) [Google Scholar]
  86. Takeuchi, H.; Sakurai, C.; Noda, R.; Sekine, S.; Murano, Y.; Wanaka, K.; Kasai, M.; Watanabe, S.; Aoyama, T.; Kondo, K. Antihypertensive effect and safety of dietary alpha-linolenic acid in subjects with high-normal blood pressure and mild hypertension. J. Oleo Sci. 2007, 56, 347–360. [Google Scholar] [CrossRef]
  87. K Kubota, T.; Matsuoka, R. Emulsion containing α-linoleic acid-rich oil suppresses the rise in blood pressure in spontaneously hypertensive rats. Jpn. Pharmacol. Ther. 2019, 47, 49–55. [Google Scholar]
  88. Oyebode, O.; Dseau, V.G.; Walker, A.; Mindell, J. Fruit and vegetable consumption and all-cause, cancer and CVD mortality: Analysis of Health Survey for England data. J. Epidemiol. Community Health 2014, 68, 856–862. [Google Scholar] [CrossRef]
  89. Yu, K.; Ke, M.Y.; Li, W.H.; Zhang, S.Q.; Fang, X.C. The impact of soluble dietary fibre on gastric emptying, postprandial blood glucose and insulin in patients with type 2 diabetes. Asia Pac. J. Clin. Nutr. 2014, 23, 210–218. [Google Scholar]
  90. Seto, Y.; Yamada, M.; Sawada, T.; Fujimoto, K. Effectiveness of ingesting shredded cabbage to fulfil the 350-g vegetable consumption quota. J. Cook. Sci. Jpn. 2014, 47, 90–96. (In Japanese) [Google Scholar]
  91. Kowata, H.; Harada, T.; Matsukubo, T.; Takaesu, Y. Influence of texture of processed foods on parotid salivary secretion and mastication. J. Jpn. Soc. Nutr. Food Sci. 1987, 40, 299–305. (In Japanese) [Google Scholar] [CrossRef]
  92. Kay, R.M. Dietary fiber. J. Lipid Res. 1982, 23, 221–242. [Google Scholar] [CrossRef] [PubMed]
  93. Jenkins, D.J.; Wolever, T.M.; Leeds, A.R.; Gassull, M.A.; Haisman, P.; Dilawari, J.; Goff, D.V.; Metz, G.L.; Alberti, K.G. Dietary fibres, fibre analogues, and glucose tolerance: Importance of viscosity. Br. Med. J. 1978, 1, 1392–1394. [Google Scholar] [CrossRef] [PubMed]
  94. Yamazaki, T.; Yamori, M.; Asai, K.; Nakano-Araki, I.; Yamaguchi, A.; Takahashi, K.; Sekine, A.; Matsuda, F.; Kosugi, S.; Nakayama, T.; et al. Mastication and risk for diabetes in a Japanese population: A cross-sectional study. PLoS ONE 2013, 8, e64113. [Google Scholar] [CrossRef]
  95. Sato, A.; Ohtsuka, Y.; Yamanaka, Y. Morning mastication enhances postprandial glucose metabolism in healthy young subjects. Tohoku J. Exp. Med. 2019, 249, 193–201. [Google Scholar] [CrossRef]
  96. Sant, M.; Allemani, C.; Sieri, S.; Krogh, V.; Menard, S.; Tagliabue, E.; Nardini, E.; Micheli, A.; Crosignani, P.; Muti, P.; et al. Salad vegetables dietary pattern protects against HER-2-positive breast cancer: A prospective Italian study. Int. J. Cancer 2007, 121, 911–914. [Google Scholar] [CrossRef]
  97. Bell, E.B.; Reis, I.M.; Cohen, E.R.; Almuhaimid, T.; Smith, D.H.; Alotaibi, F.; Gordon, C.; Fernandez, C.G.; Goodwin, W.H.; Franzmann, E.J. Green salad intake is associated with improved oral cancer survival and lower soluble CD44 levels. Nutrient 2021, 13, 372. [Google Scholar] [CrossRef]
  98. Zhang, Z.; Xu, G.; Ma, M.; Yang, J.; Liu, X. Dietary fiber intake reduces risk for gastric cancer: A meta-analysis. Gastroenterol. 2013, 145, 113–120. [Google Scholar] [CrossRef]
  99. Aune, D.; Chan, D.S.; Lau, R.; Vieira, R.; Greenwood, D.C.; Kampman, E.; Norat, T. Dietary fiber, whole grains, and risk of colorectal cancer: Systematic review and dose-response meta-analysis of prospective studies. BMJ 2011, 343, d6617. [Google Scholar] [CrossRef]
  100. Ma, Y.; Hu, M.; Zhou, L.; Ling, S.; Li, Y.; Kong, B.; Huang, P. Dietary fiber intake and risk of proximal and distal colon cancer: A meta-analysis. Medicine 2018, 97, e11678. [Google Scholar] [CrossRef]
  101. Aune, D.; Chan, D.S.M.; Greenwood, D.C.; Vieira, A.R.; Navarro Rosenblatt, D.A.; Vieira, R.; Norat, T. Dietary fiber and breast cancer risk: A systematic review and meta-analysis of prospective studies. Ann. Oncol. 2012, 23, 1394–1402. [Google Scholar] [CrossRef] [PubMed]
  102. Dong, J.Y.; He, K.; Wang, P.; Qin, L.Q. Dietary fiber intake and risk of breast cancer: A meta-analysis of prospective cohort studies. Am. J. Clin. Nutr. 2011, 94, 900–905. [Google Scholar] [CrossRef] [PubMed]
  103. Yang, J.; Wang, H.P.; Zhou, L.; Xu, C.F. Effects of dietary fiber on constipation: Meta-analysis. World J. Gastroenterol. 2012, 18, 7378–7383. [Google Scholar] [CrossRef] [PubMed]
  104. Dukas, L.; Willett, W.C.; Giovannucci, E.L. Association between physical activity, fiber intake, and other lifestyle variables and constipation in a study of women. Am. J. Gastroenterol. 2003, 98, 1790–1796. [Google Scholar] [CrossRef]
  105. Cui, J.; Lian, Y.; Zhao, C.; Du, H.; Han, Y.; Gao, W.; Xiao, H.; Zheng, J. Dietary Fibers from Fruits and Vegetables and Their Health Benefits via Modulation of Gut Microbiota. Compr. Rev. Food Sci. Food Saf. 2019, 18, 1514–1532. [Google Scholar] [CrossRef]
  106. Desai, M.S.; Seekatz, A.M.; Koropatkin, N.M.; Kamada, N.; Hickey, C.A.; Wolter, M.; Pudlo, N.A.; Kitamoto, S.; Terrapon, N.; Muller, A.; et al. A Dietary Fiber-Deprived Gut Microbiota Degrades the Colonic Mucus Barrier and Enhances Pathogen Susceptibility. Cell 2016, 167, 1339–1353. [Google Scholar] [CrossRef]
  107. Wastyk, H.C.; Fragiadakis, G.K.; Perelman, D.; Dahan, D.; Merrill, B.D.; Yu, F.B.; Topf, M.; Gonzalez, C.G.; Van Treuren, W.; Han, S.; et al. Gut-microbiota-targeted diets modulate human immune status. Cell 2021, 184, 4137–4153. [Google Scholar] [CrossRef]
  108. Frankenfeld, C.L.; Hullar, M.A.J.; Maskarinec, G.; Monroe, K.R.; Shepherd, J.A.; Franke, A.A.; Randolph, T.W.; Wilkens, L.R.; Boushey, C.J.; Le Marchand, L.; et al. The Gut Microbiome Is Associated with Circulating Dietary Biomarkers of Fruit and Vegetable Intake in a Multiethnic Cohort. J. Acad. Nutr. Diet. 2022, 122, 78–98. [Google Scholar] [CrossRef]
  109. Shabbir, U.; Rubab, M.; Daliri, E.B.-M.; Chelliah, R.; Javed, A.; Oh, D.-H. Curcumin, Quercetin, Catechins and Metabolic Diseases: The Role of Gut Microbiota. Nutrients 2021, 13, 206. [Google Scholar] [CrossRef]
  110. Mantegazza, G.; Gargari, G.; Duncan, R.; Consalez, F.; Taverniti, V.; Riso, P.; Guglielmetti, S. Ready-To-Eat Rocket Salads as Potential Reservoir of Bacteria for the Human Microbiome. Microbiol. Spectr. 2023, 11, e0297022. [Google Scholar] [CrossRef]
  111. Mantegazza, G.; Duncan, R.; Telesca, N.; Gargari, G.; Perotti, S.; Riso, P.; Guglielmetti, S. Lactic acid bacteria naturally associated with ready-to-eat rocket salad can survive the human gastrointestinal transit. Food Microbiol. 2024, 118, 104418. [Google Scholar] [CrossRef] [PubMed]
  112. Ninfali, R.; Mea, G.; Giorgini, S.; Rocchi, M.; Bacchiocca, M. Antioxidant capacity of vegetables, spices and dressings relevant to nutrition. Br. J. Nutr. 2005, 93, 257–266. [Google Scholar] [CrossRef] [PubMed]
  113. Rink, S.M.; Mendola, P.; Mumford, S.L.; Poudrier, J.K.; Browne, R.W.; Wactawski-Wende, J.; Perkins, N.J.; Enrique F Schisterman, E.F. Self-report of fruit and vegetable intake that meets the 5 a day recommendation is associated with reduced levels of oxidative stress biomarkers and increased levels of antioxidant defense in premenopausal women. J. Acad. Nutr. Diet. 2013, 113, 776–785. [Google Scholar] [CrossRef] [PubMed]
  114. Chen, Z.; Zhong, C. Oxidative stress in Alzheimer’s disease. Neurosci. Bull. 2014, 30, 271–281. [Google Scholar]
  115. Jelic, M.D.; Mandic, A.D.; Maricic, S.M.; Srdjenovic, B.U. Oxidative stress and its role in cancer. J. Cancer. Res. Ther. 2021, 17, 22–28. [Google Scholar] [CrossRef]
  116. Consumer Affairs Agency, Government of Japan. Data Base of Food with Functional Claims. Available online: https://www.fld.caa.go.jp/caaks/cssc01/ (accessed on 10 October 2024). (In Japanese).
  117. Hoy, K.; Sebastian, R.S.; Goldman, J.; Enns, C.W.; Moshfegh, A. Consuming vegetable-based salad is associated with higher nutrient intakes and diet quality among US adults, What We Eat in America, National Health and Nutrition Examination Survey 2011–2014. J. Acad. Nutr. Diet. 2019, 119, 2085–2095. [Google Scholar] [CrossRef]
  118. Su, L.J.; Arab, L. Salad and raw vegetable consumption and nutritional status in the adult US population: Results from the Third National Health and Nutrition Examination Survey. J. Am. Diet. Assoc. 2006, 106, 1394–1404. [Google Scholar] [CrossRef]
  119. Lisanias, H.; Laukapitang, L.; Tessy, C. Vegetable salad as a healthy food alternative: Organoleptic test method. J. Abdimas Nusant. 2023, 1, 28–34. [Google Scholar] [CrossRef]
  120. Landry, M.J.; Burgermaster, M.; van den Berg, A.E.; Asigbee, F.M.; Vandyousefi, S.; Ghaddar, R.; Jeans, M.R.; Yau, A.; Davis, J.N. Barriers to Preparing and Cooking Vegetables Are Associated with Decreased Home Availability of Vegetables in Low-Income Households. Nutrients 2020, 12, 1823. [Google Scholar] [CrossRef]
Figure 1. Correlation between vegetable intake and coronary heart disease incidence [7].
Figure 1. Correlation between vegetable intake and coronary heart disease incidence [7].
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Figure 2. Changes in the nutrients in carrots (fresh) during cooking, set as 100% [24].
Figure 2. Changes in the nutrients in carrots (fresh) during cooking, set as 100% [24].
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Figure 3. Effects of 400 g/day vegetable intake on body weight and LDL cholesterol level in Indonesian women [26]. Orange: control group (normal diet); blue: vegetable diet. Mean ± SEM (standard error of the mean) of 30 subjects. *: p < 0.05 vs. before intake.
Figure 3. Effects of 400 g/day vegetable intake on body weight and LDL cholesterol level in Indonesian women [26]. Orange: control group (normal diet); blue: vegetable diet. Mean ± SEM (standard error of the mean) of 30 subjects. *: p < 0.05 vs. before intake.
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Figure 4. Postprandial serum glucose and insulin levels and their IAUCs (incremental areas under the curve) in subjects fed 3 types of diets [36]. ■: vegetable salad–rice (blue), ●: vegetable salad extract–rice (yellow), ◆: rice–vegetable salad (red). Mean ± SEM of 13 subjects. # Significant difference vs. rice–vegetable salad group based on Wilcoxon signed-rank test and Bonferroni correction.
Figure 4. Postprandial serum glucose and insulin levels and their IAUCs (incremental areas under the curve) in subjects fed 3 types of diets [36]. ■: vegetable salad–rice (blue), ●: vegetable salad extract–rice (yellow), ◆: rice–vegetable salad (red). Mean ± SEM of 13 subjects. # Significant difference vs. rice–vegetable salad group based on Wilcoxon signed-rank test and Bonferroni correction.
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Figure 5. IAUC of serum β-carotene level in subjects fed 3 types of diet [53]. Yellow: carrot; blue: carrot + vegetable oil; red: carrot + mayonnaise. Mean ± SEM of 19 subjects. Different letters show a significant difference with Tukey’s test.
Figure 5. IAUC of serum β-carotene level in subjects fed 3 types of diet [53]. Yellow: carrot; blue: carrot + vegetable oil; red: carrot + mayonnaise. Mean ± SEM of 19 subjects. Different letters show a significant difference with Tukey’s test.
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Table 2. Vegetables extracted from the search results for “fresh foods” on the foods with function claims on the search site [116].
Table 2. Vegetables extracted from the search results for “fresh foods” on the foods with function claims on the search site [116].
Functional ComponentVegetables Containing Functional IngredientsFunctionalityEstimated Daily Intake of Functional Ingredients
GABATomatoFunction of maintaining memory and spatial cognition as part of cognitive function100 mg
PaprikaFunction of reducing temporary stress28 mg
SowingAbility to lower blood pressure20 mg
CabbageAbility to lower blood pressure in people with high blood pressure12.3 mg
Broccoli
Paprika
Kale
Soybean moyashi
Bean seedling
Soy isoflavoneSoybean moyashiFunction of helping maintain the components of bones23.3 mg
Function of maintaining skin moisture in middle-aged and elderly women who tend to have dry skin30 mg
LycopeneTomatoFunction of helping protect the skin from UV irritation16 mg
Ability to increase HDL cholesterol15 mg
LDL cholesterol-lowering function22 mg
InulinGarlic, chrysanthemum, chicory, burdock rootAbility to regulate physical conditions5 g
Ability to reduce postprandial glucose levels0.75 g
Function of suppressing the elevation of blood triglycerides after meals8.1 g
QuercetinCoconutFunction of helping maintain a positive mood50 mg
Sulfora glucosinolateBroccoliFunction of lowering elevated blood levels of hepatic enzymes (ALT)24 mg
Broccoli sprout
Scale plout
BroccoliAbility to increase skin moisture and relieve dryness20 mg
Broccoli sprout
Scale plout
Corin ester (acetylcholine) from eggplantSowingAbility to lower blood pressure in people with high blood pressure2.3 mg
Xanthophylls from paprikaPaprikaFunction of helping protect the skin from UV irritation9 mg
Function of helping reduce body fatness and improve BMI9 mg
LuteinSpinachFunction of protecting the eye from light-induced stimulation10 mg
KaleFunction of protecting the eye from light-induced stimulation10 mg
PumpkinFunction of protecting the eye from light-induced stimulation10 mg
KomatsunaFunction of improving contrast sensitivity (clear vision to reduce blurring)6 mg
Dietary fiber derived from tomatoTomatoAbility to reduce postprandial glucose levels1.6 g
Function of suppressing the elevation of blood triglycerides after meals1.6 g
6-gingerol, 6-gingaolGingerFunction of maintaining body temperature at peripheral sites2.35 mg
β-caroteneGreen/yellow vegetableFunction of reducing nasal discomfort caused by house dust or dust4.7 mg
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Utari, D.M.; Kartiko-Sari, I.; Miyazaki, T.; Umezawa, H.; Takeda, Y.; Oe, M.; Wang, W.; Kamoshita, S.; Shibasaki, M.; Matsuoka, R.; et al. Vegetable Salad Improves Lipid and Glucose Metabolism and Enhances Absorption of Specific Nutrients in Vegetables. Foods 2024, 13, 3591. https://doi.org/10.3390/foods13223591

AMA Style

Utari DM, Kartiko-Sari I, Miyazaki T, Umezawa H, Takeda Y, Oe M, Wang W, Kamoshita S, Shibasaki M, Matsuoka R, et al. Vegetable Salad Improves Lipid and Glucose Metabolism and Enhances Absorption of Specific Nutrients in Vegetables. Foods. 2024; 13(22):3591. https://doi.org/10.3390/foods13223591

Chicago/Turabian Style

Utari, Diah Mulyawati, Indri Kartiko-Sari, Toshitaka Miyazaki, Hiroko Umezawa, Yumi Takeda, Mariko Oe, Wei Wang, Sumiko Kamoshita, Motomi Shibasaki, Ryosuke Matsuoka, and et al. 2024. "Vegetable Salad Improves Lipid and Glucose Metabolism and Enhances Absorption of Specific Nutrients in Vegetables" Foods 13, no. 22: 3591. https://doi.org/10.3390/foods13223591

APA Style

Utari, D. M., Kartiko-Sari, I., Miyazaki, T., Umezawa, H., Takeda, Y., Oe, M., Wang, W., Kamoshita, S., Shibasaki, M., Matsuoka, R., & Yamamoto, S. (2024). Vegetable Salad Improves Lipid and Glucose Metabolism and Enhances Absorption of Specific Nutrients in Vegetables. Foods, 13(22), 3591. https://doi.org/10.3390/foods13223591

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