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Review

Is Stevia rebaudiana Bertoni a Non Cariogenic Sweetener? A Review

by
Gianmaria Fabrizio Ferrazzano
1,*,†,
Tiziana Cantile
1,2,†,
Brunella Alcidi
1,†,
Marco Coda
1,†,
Aniello Ingenito
1,†,
Armando Zarrelli
3,4,†,
Giovanni Di Fabio
3,† and
Antonino Pollio
5,†
1
Department of Neuroscience, Reproductive and Oral Sciences, Section of Paediatric Dentistry, University of Naples, Federico II, Naples 80131, Italy
2
Bambino Gesù Hospital, Division of Dentistry and Orthodontics, Rome 00165, Italy
3
Department of Chemical Sciences, Complesso Universitario di Monte Sant’Angelo, Cupa Nuova Cintia, 21-80126-Napoli, University of Naples, Federico II, Naples 80126, Italy
4
Inter-University Consortium “SannioTech”, Apollosa (BN) 82030, Italy
5
Department of Biology, Complesso Universitario di Monte Sant’Angelo, Cupa Nuova Cintia, 21-80126-Napoli, University of Naples, Federico II, Naples 80126, Italy
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2016, 21(1), 38; https://doi.org/10.3390/molecules21010038
Submission received: 6 November 2015 / Revised: 14 December 2015 / Accepted: 21 December 2015 / Published: 26 December 2015
(This article belongs to the Special Issue 20th Anniversary of Molecules—Recent Advances in Medicinal Chemistry)
Browse Figures
Versions Notes

Abstract

:
Stevia rebaudiana Bertoni is a small perennial shrub of the Asteraceae (Compositae) family that is native to South America, particularly Brazil and Paraguay, where it is known as “stevia” or “honey leaf” for its powerful sweetness. Several studies have suggested that in addition to their sweetness, steviosides and their related compounds, including rebaudioside A and isosteviol, may offer additional therapeutic benefits. These benefits include anti-hyperglycaemic, anti-hypertensive, anti-inflammatory, anti-tumor, anti-diarrheal, diuretic, and immunomodulatory actions. Additionally, critical analysis of the literature supports the anti-bacterial role of steviosides on oral bacteria flora. The aim of this review is to show the emerging results regarding the anti-cariogenic properties of S. rebaudiana Bertoni. Data shown in the present paper provide evidence that stevioside extracts from S. rebaudiana are not cariogenic. Future research should be focused on in vivo studies to evaluate the effects on dental caries of regular consumption of S. rebaudiana extract-based products.

1. Introduction

In the United States, dental caries is the most common chronic disease in children, and it is increasing in prevalence among two- to five-year-olds [1,2]. Nevertheless, caries prevalence varies from population to population. In developing countries, such as the Philippines, an early childhood caries prevalence of up to 85% has been reported for disadvantaged groups [3]. In the Western world, studies have reported that the prevalence of dental caries at three years of age was 15.4%, but strong associations were found with socioeconomic status and ethnicity [4,5].
A significant improvement in dental caries levels worldwide may be attained by the implementation of caries preventive strategies, paying special attention to high-risk groups that are represented by people with low economic-social status in developed countries and people who lives in less developed countries [6,7].
Therefore, current research is focused on the elaboration of a new methodology against dental caries that is based on the identification and the characterization of natural active compounds that have anti-caries activity, reduce cariogenic microflora pathogenicity and/or remineralize dental hard tissues [8,9,10,11,12].

2. Dental Caries Pathogenesis and Its Relation with Alimentary Factors

Sugars are recognized as the most important dietary factor in the development of dental caries. Furthermore, the role of acid fermented products of sugars in enamel dissolution by the action of bacteria, such as Streptococcus mutans and Lactobacillus casei [13], is clear. Upon fermentation by oral bacteria, sucrose molecules are transformed into energy and high quantities of acidic substances that increase the concentration of hydrogen ions, by lowering the pH, and dissolve enamel, the cementum, and dentin [14]. Thus, frequent exposure to this carbohydrates creates conditions for caries onset by promoting demineralization.
As an additional virulence mechanism, cariogenic bacteria populating the dental biofilm produce exopolysaccharides that are able to create a protective environment against the physiological antibacterial mechanisms of the mouth [15].
Since these microorganisms are the most prominent factors in the dental caries process, modifying their metabolism by reducing the production of lactic acid in the oral cavity will provide additional justification for the prevention of dental caries [16]. Numerous studies show that the form in which sugars are ingested and the frequency of their consumption are directly related to the prevalence of caries [17]. Sugars also contribute to the increase in an elevated number of health problems such as obesity and dysmetabolic diseases [18,19].

2.1. Development of Natural Sweeteners in Food Factory Research

As mentioned previously, there is a definite relationship between the dietary consumption of sucrose and the incidence of dental caries. Therefore, intensive research for a low calorie, non-cariogenic sweetener has been performed to provide an alternative compound to sugar for use in food and drugs, and several artificial sweeteners have been introduced by the food industry to sweeten food and beverages. Research for alternatives to sucrose have resulted in the development of synthetic sweeteners, many of which are considered safe for teeth, such as aspartame, saccharin, cyclamate, xylitol, and mannitol [17]. These sweeteners have also been used as sugar substitutes for caries-active patients.
However, in addition to their benefits, animal studies have proven that artificial sweeteners cause weight gain, brain tumours, bladder cancer, and many other health hazards [17]. Thus, research must continue to identify natural foods and components that protect against dental caries, particularly those that have practical dietary application and can help make dietary advice effective.
The ideal product would be calorie-free, non-carcinogenic, non-mutagenic, not heat degradable, economical to produce, and it would provide sweetness with no unpleasant aftertaste. However, obtaining these properties in a single product has been extremely challenging.
Since ancient times, active compounds from plant origins have been used as medicines for various diseases and microbial infections.
Recent research has also been oriented towards the discovery and evaluation of novel, potentially non-cariogenic, sweeteners from nature. Several highly sweet plant constituents are commercially utilized in foods and beverages as non-cariogenic sucrose substitutes in Japan and in some other Asian, European, and American countries, including the diterpene glycoside, stevioside, a steviol glycoside extracted from Stevia rebaudiana (Bertoni).

2.2. The Genus Stevia: Botanical and Ethnobotanical Remarks, with an Emphasis on S. rebaudiana Bertoni

Stevia Cav. is a genus of herbaceous and shrubby plants distributed exclusively in the American Continent, from the Southern United States to Central and South America. More than 200 species belong to this genus, which is taxonomically placed in the Tribe Eupatoriae of the family Asteraceae [20]; most species are distributed between Mexico (approximately 100) and Brazil (approximately 40). The members of Stevia occupy a range of habitats, from mountain forests (above 1000 m) to the borders of rivers and dry valleys [21], preferring semi-humid and cold climates [22]. Stevia species present a very similar morphology of inflorescence, which is composed of five small tubular flowers with numerous hairs on the inner surface of the white corollas.
In Central and South America, numerous Stevia species, such as S. salicifolia Cav. and S. lucida Lag., have long been known for their ethnopharmacological uses, ranging from anti-helminthic to anti-rheumatic and anti-inflammatory applications. Certain species are also used as an emetic (S. rhombifolia HBK), for the treatment of cardiac conditions (S. cardiatica Perkins) or as anti-diarrheal (S. balansae Hieron, S. trifida), whereas diuretic properties have been attributed to S. eupatoria (Spreng.) Willd. and S. pilosa Lag. [23]. Apparently, S. rebaudiana (Bertoni) Bertoni, which originated from Northeastern Paraguay, is a unique species containing the glycosides stevioside and rebaudioside A, responsible for the sweet taste of the leaves [24]. It is a perennial shrub, spontaneously growing in the subtropical, mesothermal and humid habitats of South America (Figure 1) [25]. The plant is rhizomatous, with a well-developed root system; the stem is erect and woody, with tiny hairs in the lower part; and the slightly pubescent leaves are sessile, with a dentate margin in the upper part of the plant and entirely at the bottom. S. rebaudiana is not common in its type locality, but it is cultivated at least in three continents (Figure 2), particularly in Asia, from China to Thailand [26].
In Paraguay, S. rebaudiana flowers from January to March, whereas in the Northern Hemisphere, the flowering time is between September and December. In its native habitat, the plant occurs mainly in sandy soils; under cultivation, however, the growth and flowering of S. rebaudiana depend on solar radiation, photoperiod, temperature and water availability of the soil [27]. When cultivated under long-day conditions, S. rebaudiana increases the foliar area and the concentration of sweetening glycosides in the leaves [28]. S. rebaudiana, often referred to as the sweet herb of Paraguay, has been widely used in many countries, including China, Japan, Korea, Brazil, and Paraguay, either as a substitute for sucrose in foods and beverages or as a household sweetening agent [29]. The plant is rich in carbohydrates (62% dry weight, dw), protein (11% dw), crude fibre (16% dw), minerals (K, Ca, Na, Mg, Cu, Mn, Fe, Zn), and essential amino acids [30].
Molecules 21 00038 g001 550
Figure 1. Countries of South America where S. rebaudiana grows spontaneously.
Figure 1. Countries of South America where S. rebaudiana grows spontaneously.
Molecules 21 00038 g001
Molecules 21 00038 g002 550
Figure 2. Regions of the world where it is possible to cultivate S. rebaudiana.
Figure 2. Regions of the world where it is possible to cultivate S. rebaudiana.
Molecules 21 00038 g002

2.3. S. rebaudiana Chemical Constituents and Extraction Procedures

The extracted active ingredient of S. rebaudiana is a white crystalline substance, and it has been used for centuries to sweeten food and beverages by the indigenous people of South America.
The compounds responsible for the natural sweetness of S. rebaudiana leaves include diverse diterpenoid glycosides derived from a steviol skeleton. These steviol glycosides also exhibit low calorific value, which is interesting for promising therapeutic applications, particularly for the treatment of disturbances in sugar metabolism.
Recently, several modern techniques have been introduced for the extraction of commercially-important stevioside metabolites from the plant. These methods were optimized in terms of temperature, duration of the process, stability and quantity of molecules extracted, whereas the conventional methods of extraction (Soxhlet extraction, hot or cold maceration, and hydro distillation) were less desirable from both an economic and an extractive standpoint (Table 1) [31,32,33].
Table
Table 1. Different extraction methods of steviosides from air dried crushed leaves of S. rebaudiana.
Table 1. Different extraction methods of steviosides from air dried crushed leaves of S. rebaudiana.
Extraction MethodProblems/Advantages/DisadvantagesRef.
Water extraction processOptimization in terms of pH, temperature, pressure, duration.[31]
Water leachingTime and labor consumption.[32]
Ethanol leachingMore rapid than water leaching, keeping the same extraction recovery.[32]
Supercritical fluid extraction (SFE)Low solvation power for polar stevioside, need to use a co-solvent. Optimization in terms of pressure and temperature.[32]
Pressurized fluid extraction (PFE)Multiple rate, lower solvent consumption, enhanced mass transfer and increased solvation power. Limited to thermally stable analytes.[32]
Pressurized hot water extraction (PHWE)/subcritical water extractionExtraction of nonpolar compounds with water, environmentally-friendly and economically-beneficial alternative to harmful organic solvents.[32]
Microwave assisted extractionOptimization in terms of solvent and solvent volume. Extraction of compounds of commercial importance in less time, with lesser solvent and causing comparatively lesser harm to the environment.[33]
Soxhlet extractionOptimization in terms of time, solvent, and solvent volume.[33]
Cold macerationOptimization in terms of time, solvent, and solvent volume.[33]
Microwave-assisted extraction uses pressurized and/or supercritical fluids or microwaves to reduce extraction time. Moreover, in microwave assisted extraction, the typical solvent volume used ranges from 10 to 30 mL per gram of plant sample, much less than that required in conventional extraction methods (Table 1) [33].
Steviosides are soluble in water, the optimal solvent, and water is the most efficient polar solvent in regard to its dielectric constant to absorb microwave energy, dissipate it in the external environment and finally promote the exudation of steviosides from the cells of leaves. Methanol and water can be used for extraction under pressure as well. Methanol is the best solvent in the temperature range of 110 to 160 °C [32]. Another important aspect is the time required for the extraction, which can vary from 16 to 24 h for Soxhlet extraction to just minutes, possibly longer, with a microwave assisted extraction.
The leaves have a stevioside contents between 4% and 20% of their dry weight, in according on the cultivar and growing conditions. The maximum amount was observed in microwave assisted extraction of S. rebaudiana leaves, while the minimum was obtained by cold maceration of the leaf powder, using water as the solvent for both methods [33].
The three major constituents of the leaf extract of S. rebaudiana were stevioside, rebaudioside A, and rebaudioside C (from 3% to 17%, by weight) [34,35]. Other compounds present at lower concentration are: steviolbioside, rebaudiosides B, D, E, F, and steviolmonoside [36,37].
Molecules 21 00038 g003 550
Figure 3. Sweetness of the most common artificial and natural sweeteners.
Figure 3. Sweetness of the most common artificial and natural sweeteners.
Molecules 21 00038 g003
Stevioside, the main sweet component in the leaves of S. rebaudiana (Bertoni) Bertoni tastes approximately 300 times sweeter than sucrose. The structures of the sweet components of S. rebaudiana, which occur primarily in the leaves, are provided in Figure 3.
Isolated steviosides can be purified using various methods including column chromatography, TLC and HPLC methods. Finally the isolated compounds were analyzed and characterized using analytical methods such as UV, FTIR, MS, and NMR analyses.

2.4. Medicinal and Alimentary Uses of S. rebaudiana Glycosides

There are three types of S. rebaudiana-based products: the regular products, which consist mainly of a stevioside; the Reva A products, which consist mainly of rebaudioside A; and the sugar metastasis product. In the regular products, the content ratio of stevioside to rebaudioside ranges from 7:3 to 8:2, while in Reva A, this ratio is approximately 1:3. Since rebaudioside has a very sweet taste, the quality of sweetness for Reva A products is higher than regular ones [38]. Steviosides offer several advantages over other non-caloric sucrose substitutes: they are heat-stable, resistant to acid hydrolysis and non-fermentable [39].
Further studies have suggested that in addition to sweetness, steviosides and their related compounds, including rebaudioside A and isosteviol (a metabolic component of stevioside), may also offer therapeutic benefits. These benefits include: anti-hyperglycaemic, anti-hypertensive, anti-oxidant [40], anti-tumor [41,42], anti-diarrheal, diuretic, gastro- [43] and renal-protective [44], anti-viral [45], and immunomodulatory [46,47] actions. (Table 2 and Table 3).
Table
Table 2. Medicinal uses of Stevia species [48,49].
Table 2. Medicinal uses of Stevia species [48,49].
SpeciesMedicinal Uses
S. balansae Hieron.Intestinal affections
S. cardiatica PerkinsCardiac affections
S. connata Lag.Gastric affections
S. elatior H. B. KVulnerary, Dermatologic affections
S. eupatoria (Spreng.) Willd.Renal affections
S. glandulosa Hook. & Arn.Antipyretic, Cold
S. lucida Lag.Anti-inflammatory, Anti-dolorific, Flue, Vulnerary
S. macbridei B. L. Rob.Gynecologic affections
S. nepetifolia H. B. K.Gynecologic affections
S. pilosa Lag.Antipyretic, Intestinal affections, Renal affections
S. plummense A. GrayVulnerary
S. puberula Hook.Gastric affections
S. rebaudiana (Bert.) BertoniGynecologic affections, Anti-diabetic
S. rhombifolia KunthGastric affections
S. salicifolia Cav.Anti-rheumatic, Intestinal affections, Cold
S. serrata Cav.Vulnerary, Anti-cough
S. subpubescens Lag.Anti-dolorific, Gynecologic affections, Gastric affections
S. trifida Lag.Gastrointestinal affections
Table
Table 3. Medicinal uses of Stevia species.
Table 3. Medicinal uses of Stevia species.
Medicinal PropertiesRef.
Anti-hyperglycemic/Anti-diabetic[40]
Anti-Inflammatory[47]
Antimicrobial[41]
Antioxidant[40]
Antitumor[42]
Antiviral[45]
Immunomodulatory[46]
Gastroprotective activity[43]
Renal protective[44]
Fengyang et al. [50] examined the anti-inflammatory proprieties of stevioside and discovered that stevioside exerts its anti-inflammatory effect by inhibiting the activation of NF-κB and mitogen-activated protein kinase signaling and the release of pro-inflammatory cytokines (Table 2 and Table 3).
The effects of stevioside and its metabolite, steviol, on human colon carcinoma cell lines were studied from Boonkaewwan et al. [51] in 2008. Their results demonstrated two biological effects of steviol in the colon: the stimulation of Cl(−) secretion and the attenuation of TNF-alpha stimulated IL-8 production.
The anti-hyperglycaemic and blood pressure-reducing effects of S. rebaudiana were investigated in 2003 by Jeppesen et al. [52] in a long-term study of type 2 diabetic Goto-Kakizaki (GK) rats. According to their results, stevioside may determine an increasing of insulin secretion, inducting genes involved in glycolysis. It can also: improve the nutrient-sensing mechanisms, rise cytosolic long-chain fatty acyl-coenzyme A (CoA), and control down-regulation of phosphodiesterase 1 (PDE1). They concluded that stevioside demonstrates a dual positive effect: both antihyperglycemic and blood pressure-lowering actions.
As mentioned above, the steviol glycoside is currently used in several countries as a sweetener, and it has been extensively tested to demonstrate that its use is safe for humans. In 2002, S. rebaudiana ranked second in the sales of herbal supplements in the USA.
According to the Joint FAO/WHO Expert Committee on Food Additives (JECFA, 2004), the consumption of S. rebaudiana has been generally regarded as safe [53].
Aqueous extracts of S. rebaudiana leaves have been approved since 2008 by the JECFA as sugar substitutes in many foods and beverages in the Western and Far East Asian countries. However, JECFA has requested additional information to change the temporary accepted daily intake (ADI) of 0–2 mg·kg−1·day−1 for steviol glycoside. The European Union approved stevia additives in 2011 [54].
A review of several internet databases and websites was conducted to identify literature related to the antimicrobial effects of stevioside extract and its role in caries prevention and dental health promotion. The keywords that were used individually or in combination included: dental caries, sweeteners, non-caloric sweeteners, stevia, stevioside, and antimicrobial activity.

2.5. Caries Prevention Activity of S. rebaudiana Extracts and Steviol Glycosides

Presently, S. rebaudiana is the only species of the genus with recognized antibiotic properties. The antimicrobial effects of S. rebaudiana have been ascribed to the presence of stevioside and related compounds, but their role in caries prevention and dental health promotion is not fully understood. In 2010, Mohire and Yadav [55] conducted a four week clinical study in patients with oro-dental problems to develop a chitosan-based polyherbal toothpaste (including S. rebaudiana extract). They also evaluated its plaque-reducing ability and efficacy in the reduction of dental pathogens using chlorhexidine gluconate (0.2% w/v) mouthwash as the positive control.
The study involved 18 subjects who were divided into three groups. The groups were treated as follows: Group-I, placebo, toothpaste without chitosan and herbal ingredients; Group-II, positive control, CHX (0.2% w/v) mouthwash; and Group-III, test (Polyherbal), toothpaste with chitosan, eugenol, and Pterocarpus marsupium (PM), S. rebaudiana, and Glycyrrhiza glabra aqueous extracts. Authors determined the total microbial count in order to obtain the reduction, in percentage, of oral bacterial count during the treatment period.
At the end of the study, the herbal extracts were shown to possess satisfactory antimicrobial activity against most of the dental pathogens. The chitosan-containing polyherbal toothpaste significantly reduced the plaque index from 70% to 47% and the bacterial count from 85% to 29%.
The authors concluded that chitosan-based polyherbal toothpaste represented a promising novel oral hygiene product compared with the currently available oral hygiene products. Nevertheless, in this study, the role of S. rebaudiana in reducing antimicrobial count is not clear: this effect, in fact, could be the result of synergic action of all active principles involved in the toothpaste.
In 2013, Giacaman et al. [56] investigated the cariogenic and enamel demineralization potential of several sweeteners in an artificial caries model.
Bovine enamel slabs were utilized as the culture medium for S. mutans UA159 biofilm that were exposed to different sweeteners in powder or tablet form, as including S. rebaudiana extracts, sucralose, saccharin, aspartame, and fructose, three times a day for five minutes The caries-positive and caries-negative controls were 10% sucrose and 0.9% NaCl, respectively. After five days, the biomass, bacterial counts, and intra- and extracellular polysaccharides of the biofilm were assessed. Surface microhardness was measured before and after the experiment to evaluate enamel demineralization, which was expressed as percentage of surface hardness loss (%SHL). The results of this study suggest less cariogenic effects and enamel demineralization for all tested sweeteners except sucrose. Compared to sucrose, S. rebaudiana extracts, sucralose and saccharin reduced the number of viable cells (p < 0.05), and all sugar alternative sweeteners reduced extracellular polysaccharide formation. Nevertheless the primary limitation of this study is that the artificial substrate does not allow a biofilm formation rate comparable with a real clinical situation.
In 2012, Gamboa and Chaves [57] evaluated the antibacterial activity of S. rebaudiana leaf extracts against cariogenic bacteria. They prepared extracts from dried leaves in hexane, methanol, ethanol, ethyl acetate, and chloroform, and they evaluated, using well diffusion method, the antibacterial capability of the five extracts for 16 bacterial strains of the genera Streptococcus (n = 12) and Lactobacillus (n = 4).Lactobacilli were the most sensitive, with an inhibition zone between 12.3 and 17.33 mm. Moreover, Blauth de Slavutzky [58] conducted an in vivo study to evaluate the accumulation of dental plaque after rinsing with a solution of 10% sucrose four times daily for five days and compared it to rinsing with the same frequency using a 10% solution of S. rebaudiana extract, which was prepared with 100 g of stevia boiled for 2 h in 3 L of distilled water. Consequently, it was demonstrated that S. rebaudiana, after rinsing, reduced dental plaque between 57%–82% less than sucrose solution, when measured by Silness-Löe index and 10%–40% less when measured by O’Leary index of plaque.
In 2014, Brambilla et al. [16] evaluated the effect of S. rebaudiana extracts on in vitro S. mutans biofilm formation and the in vivo pH of plaque. Three separate 10% solutions of stevioside, rebaudioside A and sucrose were prepared. The microbological count in vivo was measured using a MTT assay. Twenty volunteers rinsed with each solution for one minute and then the plaque Ph was analyzed seven times after the rinses. Higher in vitro S. mutans biofilm formation was observed with the sucrose solution (p < 0.01). After 5, 10, 15, and 30 min, the in vivo sucrose rinse produced a statistically significantly lower pH value compared to the S. rebaudiana extracts (F = 99.45, p < 0.01). Therefore, S. rebaudiana extracts can also be considered non-acidogenic [16].
In 1992, Das et al. [59] tested stevioside and rebaudioside A for cariogenicity in albino Sprague-Dawley rats. The authors divided sixty rat pups colonized with S. sobrinus into four groups and fed them their basal diets with added stevioside, rebaudioside A or sucrose as follows: group 1, 30% sucrose; group 2, 0.5% stevioside; group 3, 0.5% rebaudioside A; and group 4, no additional chemicals. Significant differences resulted in sulcal caries scores and S. sobrinus counts between group 1 and the other three groups. In fact, there was no significant difference between the stevioside, rebaudioside A and no-addition groups. Thus, neither stevioside nor rebaudioside A were cariogenic under the conditions of the study, whose primary limitation is the use of a not human sample.
Zanela et al. [60] investigated the effect of daily mouth-rinse use on dental plaque accumulation and on salivary S. mutans in 200 children in 2002. The solutions used were: a placebo solution composed of mentholated deionized water (group I); 0.12% chlorhexidine gluconate associated to 0.05% sodium fluoride (group II); 0.2% chlorhexidine digluconate (group III); and 0.5% stevioside mixed with 0.05% sodium fluoride at pH 3.4 (group IV). To verify the accumulation of plaque, it was assessed the Löe index method at the beginning and end of the experiment. Moreover, the analysis of cariogenic streptococci was accomplished on three saliva samples collected at three different times: before the first mouth-rinse, 24 h after the first mouth-rinse and one week after the last mouth-rinse. The mouth-rinsing routine was performed daily for 4 weeks.
The solution used by group III was the least accepted by children. Furthermore, as solution II was utilized by group II, it caused mild dental pigmentation. There were no statistically significant differences in the levels of S. mutans, most likely due to the low initial levels observed in each of the four groups (Table 4).
Table
Table 4. Caries prevention activity of S. rebaudiana extracts and steviol glycosides.
Table 4. Caries prevention activity of S. rebaudiana extracts and steviol glycosides.
SourceType of StudyResultsRef.
S. rebaudiana aqueous extractIn vivoReduction of plaque index by 70.47%.[56]
S. rebaudiana aqueous extractsIn vitroReduction of extracellular polysaccharide formation.[57]
S. rebaudiana methanol and ethanol extractsIn vitroInhibition of growth of Lactobacilli.[58]
S. rebaudiana aqueous extractsIn vivoReduction of plaque index.[59]
S. rebaudiana aqueous extractsIn vitro and in vivoS. rebaudiana extracts are non-acidogenic.[16]
Solution containing 0.5% Stevioside and Rebaudioside AIn vivoDental plaque reduction was not evident using stevioside mouth rinses.[61]
Stevioside extractsIn vitroStevioside and rebaudioside A are not cariogenic.[60]

3. Future Research

Despite advances made in the fluoridation of water and in the dispersal of oral hygiene standards, dental caries still remains a major health problem, affecting all countries worldwide. Because the current therapeutic strategies to prevent dental diseases are not entirely void of side effects, it should be necessary to develop new alternative approaches for clinical bacterial control. Recent research has demonstrated that plant extracts may be a suitable alternative treatment for caries [61,62,63,64,65]. Several plants products have been studied for their capability to contrast dental plaque formation, but a very limited number of these natural products has found therapeutic application, such as compounds rich in polyphenols [62].
Data shown in present review evidence that stevioside extracts from S. rebaudiana are not cariogenic in adult population. However, future research should be focused on in vivo studies to evaluate the effects of regular consumption of S. rebaudiana extract-based products on dental caries both in adult and pediatric population.

Author Contributions

G. Ferrazzano and A. Pollio proposed the study, A. Ingenito edited the manuscript. T. Cantile, B. Alcidi and M. Coda A. wrote the paragraphs related to medical and anti-caries activity of Stevia Rebaudiana Bertoni. Pollio wrote botanical and ethnobotanical paragraphs of the manuscript. A. Zarrelli and G. Di Fabio wrote chemical paragraphs and related tables and figures of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Bourgeois, D.M.; Llodra, J.C. Global burden of dental condition among children in nine countries participating in an international oral health promotion programme, 2012–2013. Int. Dent. J. 2014, 64, 27–34. [Google Scholar] [CrossRef] [PubMed]
  2. Dye, B.A.; Tan, S.; Smith, V.; Lewis, B.G.; Barker, L.K.; Thornton-Evans, G.; Eke, P.I.; Beltrán-Aguilar, E.D.; Horowitz, A.M.; Li, C.H. Trends in oral health status: United States, 1988–1994 and 1999–2004. Vital Health Stat. 2007, 248, 1–92. [Google Scholar]
  3. Cariño, K.M.; Shinada, K.; Kawaguchi, Y. Early childhood caries in northern Philippines. Commun. Dent. Oral Epidemiol. 2003, 31, 81–89. [Google Scholar] [CrossRef]
  4. Ferro, R.; Besostri, A.; Meneghetti, B.; Olivieri, A.; Benacchio, L.; Tabaccanti, S.; Mazzoleni, S.; Favero, G.; Stellini, E. Oral health inequalities in preschool children in North-Eastern Italy as reflected by caries prevalence. Eur. J. Paediatr. Dent. 2007, 8, 13–18. [Google Scholar] [PubMed]
  5. Ferrazzano, G.F.; Scaravilli, M.S.; Ingenito, A. Dental and periodontal health status in Campanian children and relation between caries experience and socio-economic behavioural factors. Eur. J. Paediatr. Dent. 2006, 7, 174–178. [Google Scholar] [PubMed]
  6. Ferrazzano, G.F.; Sangianantoni, G.; Cantile, T.; Ingenito, A. Relationship between social and behavioural factors and caries experience in schoolchildren in Italy. Oral Health Prev. Dent. 2015. [Google Scholar] [CrossRef]
  7. Folayan, M.O.; Kolawole, K.A.; Oziegbe, E.O.; Oyedele, T.; Oshomoji, O.V.; Chukwumah, N.M.; Onyejaka, N. Prevalence, and early childhood caries risk indicators in preschool children in suburban Nigeria. BMC Oral Health 2015, 15, 72. [Google Scholar] [CrossRef] [PubMed]
  8. Jeon, J.G.; Rosalen, P.L.; Falsetta, M.L.; Koo, H. Natural products in caries research: Current (limited) knowledge, challenges and future perspective. Caries Res. 2011, 45, 243–263. [Google Scholar] [CrossRef] [PubMed]
  9. Ferrazzano, G.F.; Amato, I.; Cantile, T.; Sangianantoni, G.; Ingenito, A. In vivo remineralising effect of GC tooth mousse on early dental enamel lesions: SEM analysis. Int. Dent. J. 2011, 61, 210–216. [Google Scholar] [PubMed]
  10. Ferrazzano, G.F.; Roberto, L.; Amato, I.; Cantile, T.; Sangianantoni, G.; Ingenito, A. Antimicrobialproperties of green tea extract against cariogenic microflora: An in vivo study. J. Med. Food 2011, 14, 907–911. [Google Scholar] [CrossRef] [PubMed]
  11. Ferrazzano, G.F.; Cantile, T.; Quarto, M.; Ingenito, A.; Chianese, L.; Addeo, F. Protective effect of yogurt extract on dental enamel demineralization in vitro. Aust. Dent. J. 2008, 53, 314–319. [Google Scholar] [CrossRef] [PubMed]
  12. Mirpour, M.; Siahmazgi, Z.G.; Kiasaraie, M.S. Antibacterial activity of clove, gall nut methanolic and ethanolic extracts on Streptococcus mutans PTCC 1683 and Streptococcus salivarius. J. Oral Biol. Craniofac. Res. 2015, 5, 7–10. [Google Scholar] [CrossRef] [PubMed]
  13. Sheiham, A.; James, W.P.T. A reappraisal of the quantitative relationship between sugar intake and dental caries: The need for new criteria for developing goals for sugar intake. BMC Public Health. 2014, 14, 863. [Google Scholar] [CrossRef] [PubMed]
  14. Kawashita, Y.; Kitamura, M.; Saito, T. Early childhood caries. Int. J. Dent. 2011, 725320. [Google Scholar] [CrossRef] [PubMed]
  15. Giacaman, R.A.; Contzen, M.P.; Yuri, J.A.; Muñoz-Sandoval, C. Anticaries effect of an antioxidant-rich apple concentrate on enamel in an experimental biofilm-demineralization model. J. Appl. Microbiol. 2014, 117, 846–853. [Google Scholar] [CrossRef] [PubMed]
  16. Brambilla, E.; Cagetti, M.G.; Ionescu, A.; Campus, G.; Lingström, P. An in vitro and in vivo comparison of the effect of Stevia rebaudiana extracts on different caries-related variables: A randomized controlled trial pilot study. Caries Res. 2014, 48, 19–23. [Google Scholar] [CrossRef] [PubMed]
  17. Gupta, P.; Gupta, N.; Pawar, A.P.; Birajdar, S.S.; Natt, A.S.; Singh, H.P. Role of sugar and sugar substitutes in dental caries: A review. ISRN Dent. 2013, 29. [Google Scholar] [CrossRef] [PubMed]
  18. Raben, A.; Vasilaras, T.H.; Møller, A.C.; Astrup, A. Sucrose compared with artificial sweeteners: Different effects on ad libitum food intake and body eight after 10 wk of supplementation in overweight subjects. Am. J. Clin. Nutr. 2002, 76, 721–729. [Google Scholar] [PubMed]
  19. Laville, M.; Nazare, J.A. Diabetes, insulin resistance and sugars. Obes. Rev. 2009, 10, 24–33. [Google Scholar] [CrossRef] [PubMed]
  20. Gentry, A.H. A Field Guide of the Families and Genera of Woody Plants of Northwest South America (Colombia, Ecuador, Peru) with Supplementary Notes on Herbaceus Taxa; The University of Chicago Press: Chicago, IL, USA, 1996; p. 895. [Google Scholar]
  21. Robinson, R.L. Contributions from the Gray Herbarium of Harvard University XC; The Gray Herbarium of Harvard University: Cambridge, MA, USA, 1930; pp. 78–91. [Google Scholar]
  22. Watanabe, K.; Yahara, T.; Denda, T.; Kosuge, K. Chromosomal evolution in the genus Brachyscome (Asteraceae, Astereae): Statistical tests regarding correlation between changes in karyotype and habit using phylogenetic information. J. Plant Res. 1999, 112, 145–146. [Google Scholar] [CrossRef]
  23. Soejarto, D.D.; Compadre, C.M.; Medon, P.J.; Kamath, S.K.; Kinghorn, A.D. Potential sweetening agents of plant origin. II. Field search for sweet-tasting Stevia species. Econ. Bot. 1983, 37, 71–79. [Google Scholar] [CrossRef]
  24. Lemus-Mondaca, R.; Vega-Gálvez, A.; Zura-Bravo, L.; Ah-Hen, K. Stevia rebaudiana Bertoni, source of a high-potency natural sweetener: A comprehensive review on the biochemical, nutritional and functional aspects. Food Chem. 2012, 132, 1121–1132. [Google Scholar] [CrossRef]
  25. Kinghorn, A.D. Stevia: The Genus Stevia; CRC Press: Boca Raton, FL, USA, 2003; p. 224. [Google Scholar]
  26. Chatsudthipong, V.; Muanprasat, C. Stevioside and related compounds: Therapeutic benefits beyond sweetness. Pharmacol. Ther. 2009, 121, 41–54. [Google Scholar] [CrossRef] [PubMed]
  27. Ramesh, K.; Singh, V.; Megeji, N.W. Cultivation of Stevia [Stevia rebaudiana (Bert.) Bertoni]: A comprehensive review. Adv. Agron. 2006, 89, 137–177. [Google Scholar]
  28. Singh, S.D.; Rao, G.P. Stevia: The herbal sugar of 21st Century. Sugar Tech 2005, 7, 17–24. [Google Scholar] [CrossRef]
  29. Soejarto, D.D. Botany of Stevia and Stevia rebaudiana. In Stevia. The genus Stevia, 1st ed.; Kinghorn, A.D., Ed.; Taylor & Francis Inc.: New York, NY, USA, 2002; pp. 18–39. [Google Scholar]
  30. Aminha, S.; Soumya, A.N.; Raju, V.G.; Goud, B.M.; Irfath, M.; Quadri, S.A.P. Isolation and extraction of artificial sweetner (Stevia). World J. Pharm. Res. 2014, 3, 481–486. [Google Scholar]
  31. Rao, A.B.; Reddy, G.R.; Ernala, P.; Sridhar, S.; Ravikumar, Y.V.L. An improvised process of isolation, purification of steviosides from Stevia rebaudiana Bertoni leaves and its biological activity. Int. J. Food Sci. Technol. 2012, 47, 2554–2560. [Google Scholar] [CrossRef]
  32. Pol, J.; Varadova, O.E.; Karasek, P.; Roth, M.; Benesova, K.; Kotlarikova, P.; Caslavsky, J. Comparison of two different solvents employed for pressurized fluid extraction of stevioside from Stevia rebaudiana: Methanol versus water. Anal. Bioanal. Chem. 2007, 388, 1847–1857. [Google Scholar] [CrossRef] [PubMed]
  33. Javad, S.; Naz, S.; Ilyas, S.; Tariq, A.; Aslam, F. Optimization of the microwave assisted extraction and its comparison with different conventional extraction methods for isolation of stevioside from Stevia rebaudiana. Asian J. Chem. 2014, 26, 8043–8048. [Google Scholar]
  34. Kolb, N.; Herrera, J.L.; Ferreyra, D.J.; Uliana, R.F. Analysis of sweet diterpene glycosides from Stevia rebaudiana: Improved HPLC method. J. Agr. Food Chem. 2001, 49, 4538–4541. [Google Scholar] [CrossRef]
  35. Morlock, G.E.; Meyer, S.; Zimmermann, B.F.; Roussel, J.M. High-performance thin-layer chromatography analysis of steviol glycosides in Stevia formulations and sugar-free food products, and benchmarking with (ultra) high-performance liquid chromatography. J. Chromatogr. 2014, 1350, 102–111. [Google Scholar] [CrossRef] [PubMed]
  36. Chaturvedula, V.S.P.; Prakash, I. A new diterpene glycoside from Stevia rebaudiana. Molecules 2011, 16, 2937–2943. [Google Scholar] [CrossRef] [PubMed]
  37. Ohta, M.; Sasa, S.; Inoue, A.; Tamai, T.; Fujita, I.; Morita, K.; Matsuura, F. Characterization of novel steviol glycosides from leaves of Stevia rebaudiana. J. Appl. Glycosci. 2010, 57, 199–209. [Google Scholar] [CrossRef]
  38. Matsukubo, T.; Takazoe, I. Sucrose substitutes and their role in caries prevention. Int. Dent. J. 2006, 56, 119–130. [Google Scholar] [CrossRef] [PubMed]
  39. Giongo, F.C.; Mua, B.; Parolo, C.C.; Carlén, A.; Maltz, M. Effects of lactose-containing stevioside sweeteners on dental biofilm acidogenicity. Braz. Oral Res. 2014, 28, S1806–S8324. [Google Scholar] [CrossRef] [PubMed]
  40. Kelmer, B.A.; Alvarez, M.; Brancht, A. Effects of Stevia rebaudiana natural products on rat liver mithocondria. Biochem. Pharmacol. 1985, 34, 873–882. [Google Scholar]
  41. Jayaraman, S.; Manoharan, M.S.; Illanchezian, S. In-vitro Antimicrobial and antitumor activities of Stevia rebaudiana (Asteraceae) leaf extracts. Trop. J. Pharm. Res. 2008, 7, 1143–1149. [Google Scholar] [CrossRef]
  42. Mizushina, Y.; Akihisa, T.; Ukiya, M.; Hamasaki, Y.; Nakai, C.M.; Kuriyama, I.; Tkeuchi, T.; Sugawara, F.; Yoshida, H. Structural analysis of isosteviol and related compounds as DNA polymerase and DNA topoisomerase inhibitors. Life Sci. 2005, 77, 2127–2140. [Google Scholar] [CrossRef] [PubMed]
  43. Shiozaki, K.; Fujii, A.; Nakano, T.; Yamaguchi, T.; Dato, M. Inhibitory effects of hot water extract of the Stevia stem on the contractile response of the smooth muscle of the guinea pig ileum. Biosci. Biotechnol. Biochem. 2006, 70, 489–494. [Google Scholar] [CrossRef] [PubMed]
  44. Melis, M.S. Chronic administration of aqueous extract of Stevia rebaudiana in rats: Renal effects. J. Ethnopharmacol. 1995, 47, 129–134. [Google Scholar] [CrossRef]
  45. Takahashi, K.; Matsuda, N.; Ohashi, K.; Taniguchi, K.; Nakagomi, O.; Abe, Y.; Mori, S.; Okutani, N.K.; Shigeta, S. Analysis of anti-rotavirus activity of extract from Stevia rebaudiana. Antivir. Res. 2001, 49, 15–24. [Google Scholar] [CrossRef]
  46. Sehar, I.; Kaul, A.; Bani, S.; Pal, H.C.; Saxena, A.K. Immune up regulatory response of a non-caloric natural sweetener, stevioside. Chem. Biol. Interact. 2008, 173, 115–121. [Google Scholar] [CrossRef] [PubMed]
  47. Boonkaewwan, C.; Toskulkao, C.; Vongsakul, M.J. Antinflammatory and immunomodulatory activities of stevioside and its metabolite steviol on THP-1 cells. J. Agric. Food Chem. 2006, 54, 785–789. [Google Scholar] [CrossRef] [PubMed]
  48. Soejarto, D.; Compadre, C.M.; Kinghorn, A.D. Ethnobotanical Notes on Stevia; Botanical Museum Leaflets Harvard University: Cambridge, MA, USA, 1983; pp. 1–25. [Google Scholar]
  49. Soejarto, D.D. Ethnobotany of Stevia and Stevia rebaudiana. In Stevia. The Genus Stevia; Kinghorn, A.D., Ed.; CRC Press: London, UK; New York, NY, USA, 2001; pp. 40–67. [Google Scholar]
  50. Fengyang, L.; Yunhe, F.; Bo, L.; Zhicheng, L.; Depeng, L.; Dejie, L.; Wen, Z.; Yongguo, C.; Naisheng, Z.; Xichen, Z.; Zhengtao, Y. Stevioside suppressed inflammatory cytokine secretion by downregulation of NF-κB and MAPK signalling pathways in LPS-stimulated RAW264.7 cells. Inflammation 2012, 35, 1669–1675. [Google Scholar] [CrossRef] [PubMed]
  51. Boonkaewwan, C.; Ao, M.; Toskulkao, C.; Rao, M.C. Specific Immunomodulatory and Secretory Activities of Stevioside and Steviol in Intestinal Cells. J. Agric. Food Chem. 2008, 56, 3777–3784. [Google Scholar] [CrossRef] [PubMed]
  52. Jeppesen, P.B.; Gregersen, S.; Rolfsen, S.E.; Jepsen, M.; Colombo, M.; Agger, A.; Xiao, J.; Kruhoffer, M.; Orntoff, T.; Hermansen, K. Antihyperglycemic and blood pressure-reducing effects of stevioside in the diabetic Goto-Kakizaki rat. Metabolism 2003, 52, 372–378. [Google Scholar] [CrossRef] [PubMed]
  53. Tandel, K.R. Sugar substitutes: Health controversy over perceived benefits. J. Pharmacol. Pharmacother. 2011, 2, 236–243. [Google Scholar] [CrossRef] [PubMed]
  54. Beck, A.; Cabaret, J.; Halberg, N.; Ivanova-Peneva, S.; Jespersen, L.M. Joint FAO/WHO Expert Committee on Food Additives 2008. Commission Regulation (EU) No 1131/2011 of 11 November 2011 amending Annex II to Regulation (EC) No 1333/2008 of the European Parliament and of the Council with regard to steviol glycosides. Off. J. Eur. Union 2011, 54, 207. [Google Scholar]
  55. Mohire, N.C.; Yadav, A.V. Chitosan-based polyherbal toothpaste: As novel oral hygiene product. Indian J. Dent. Res. 2010, 21, 380–384. [Google Scholar] [CrossRef] [PubMed]
  56. Giacaman, R.A.; Campos, P.; Muñoz-Sandoval, C.; Castro, R.J. Cariogenic potential of commercial sweeteners in an experimental biofilm caries model on enamel. Arch. Oral. Biol. 2013, 58, 1116–1122. [Google Scholar] [CrossRef] [PubMed]
  57. Gamboa, F.; Chaves, M. Antimicrobial potential of extracts from Stevia rebaudiana leaves against bacteria of importance in dental caries. Acta Odontol. Latinoam. 2012, 25, 171–175. [Google Scholar] [PubMed]
  58. De Slavutzky, S.M.B. Stevia and sucrose effect on plaque formation. J. Verbr. Lebensm. 2010, 5, 213–216. [Google Scholar] [CrossRef]
  59. Das, S.; Das, A.K.; Murphy, R.A.; Punwani, I.C.; Nasution, M.P.; Kinghorn, A.D. Evaluation of the cariogenic potential of the intense natural sweeteners stevioside and rebaudioside A. Caries Res. 1992, 26, 363–366. [Google Scholar] [CrossRef] [PubMed]
  60. Zanela, N.L.; Bijella, M.F.; Rosa, O.P. The influence of mouthrinses with antimicrobial solutions on the inhibition of dental plaque and on the levels of mutans streptococci in children. Pesqui. Odontol. Bras. 2002, 16, 101–106. [Google Scholar] [CrossRef] [PubMed]
  61. Ferrazzano, G.F.; Cantile, T.; Roberto, L.; Ingenito, A.; Catania, M.R.; Roscetto, E.; Palumbo, G.; Zarrelli, A.; Pollio, A. Determination of the in vitro and in vivo antimicrobial activity on salivary Streptococci and Lactobacilli and chemical characterisation of the phenolic content of a Plantago lanceolata infusion. Biomed. Res. Int. 2015, 2015. [Google Scholar] [CrossRef] [PubMed]
  62. Ferrazzano, G.F.; Roberto, L.; Catania, M.R.; Chiaviello, A.; De Natale, A.; Roscetto, E.; Pinto, G.; Pollio, A.; Ingenito, A.; Palumbo, G. Screening and scoring of antimicrobial and biological activities of italian vulnerary plants against major oral pathogenic bacteria. Evid. Based Complement. Altern. Med. 2013, 2013. [Google Scholar] [CrossRef] [PubMed]
  63. Palombo, E.A. Traditional medicinal plant extracts and natural products with activity against oral bacteria: Potential application in the prevention and treatment of oral diseases. Evid. Based Complement. Altern. Med. 2011, 2011. [Google Scholar] [CrossRef] [PubMed]
  64. Ferrazzano, G.F.; Amato, I.; Ingenito, A.; de Natale, A.; Pollio, A. Anti-cariogenic effects of polyphenols from plant stimulant beverages (cocoa, coffee, tea). Fitoterapia 2009, 80, 255–262. [Google Scholar] [CrossRef] [PubMed]
  65. Bonifait, L.; Grenier, D. Cranberry polyphenols: Potential benefits for dental caries and periodontal disease. J. Can. Dent. Assoc. 2010, 76, a130. [Google Scholar] [PubMed]

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MDPI and ACS Style

Ferrazzano, G.F.; Cantile, T.; Alcidi, B.; Coda, M.; Ingenito, A.; Zarrelli, A.; Di Fabio, G.; Pollio, A. Is Stevia rebaudiana Bertoni a Non Cariogenic Sweetener? A Review. Molecules 2016, 21, 38. https://doi.org/10.3390/molecules21010038

AMA Style

Ferrazzano GF, Cantile T, Alcidi B, Coda M, Ingenito A, Zarrelli A, Di Fabio G, Pollio A. Is Stevia rebaudiana Bertoni a Non Cariogenic Sweetener? A Review. Molecules. 2016; 21(1):38. https://doi.org/10.3390/molecules21010038

Chicago/Turabian Style

Ferrazzano, Gianmaria Fabrizio, Tiziana Cantile, Brunella Alcidi, Marco Coda, Aniello Ingenito, Armando Zarrelli, Giovanni Di Fabio, and Antonino Pollio. 2016. "Is Stevia rebaudiana Bertoni a Non Cariogenic Sweetener? A Review" Molecules 21, no. 1: 38. https://doi.org/10.3390/molecules21010038

APA Style

Ferrazzano, G. F., Cantile, T., Alcidi, B., Coda, M., Ingenito, A., Zarrelli, A., Di Fabio, G., & Pollio, A. (2016). Is Stevia rebaudiana Bertoni a Non Cariogenic Sweetener? A Review. Molecules, 21(1), 38. https://doi.org/10.3390/molecules21010038

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