Next Article in Journal
Effect of the Strain Rate on the Fracture Behaviour of High Pressure Pre-Charged Samples
Previous Article in Journal
A Highly Sensitive Impedimetric Metamitron Microsensor Based on All-Solid-State Membrane Using a New Ion-Pair Complex, [3,3′-Co(1,2-closo-C2B9H11)2][C10H11ON4]+
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Proceeding Paper

Momordica and Pycnogenol Can Tolerate Imazamox Induced Toxicity in L929 Cells Line: In Vitro Study †

by
Ali Taghizadehghalehjoughi
1 and
Betul Cicek
2,*
1
Department of Pharmacology and Toxicology, Ataturk University Faculty of Veterinary Medicine, 25100 Erzurum, Turkey
2
Department of Physiology, Ataturk University Faculty of Medicine, 25100 Erzurum, Turkey
*
Author to whom correspondence should be addressed.
Presented at the 2nd International Cell Death Research Congress, Izmir, Turkey, 1–4 November 2018.
Proceedings 2018, 2(25), 1584; https://doi.org/10.3390/proceedings2251584
Published: 11 December 2018
(This article belongs to the Proceedings of The 2nd International Cell Death Research Congress)

Abstract

:
Undesirable side effects that result from the random use of herbicides in developing countries are widespread. Imazamox is a widely used herbicide and has toxic effect on humans. Momordica charantia has been reported to possess many benefits and medicinal properties. Pycnogenol (PYC) is a natural plant extract from the bark of Pinus pinaster Aiton and has potent antioxidant activities. The aim of this study was to evaluate the protective effects of pycnogenol and momardica on induced imazamox toxicity effects on L929 fibroblast cell line. L929 fibroblast cells were cultured in the appropriate culture medium. Toxic concentration of imazamox 250 μM, were administered 30 min prior to momordica and pycnogenol (10−1–10−5 concentration) on L929 fibroblast cell line for 24 h. The cell viability assay was determined by using MTT test. TAC-TOS analysis were used to evaluate antioxidant and oxidant status. According to our study pycnogenol high dose showned protective effect whereas momordica low dose showned protective effect p < 0.05. In current study pycnogenol increased TAC capacity in high dose but in lower dose pycnogenol did not show any promise (p < 0.05). Momordica results showed correlation with MTT result. According to this analyse momordica only in low dose increased anti oxidant capacity and in addition, only in low dose TOS level were decreased (p > 0.05). In conclusion momordica and pycnogenol showed promise to reduced imazamox toxicity.
Keywords:
L929; momordica; imazomox

1. Introduction

In today’s world, the use of herbicide has become so important that their use is inextricably linked with improvement of human welfare. Despite of all the advantages of herbicides, there is worldwide concern about their use because of not specific targeting of herbicides. Imazamox is a member of the imidazolinone class of chemicals including imazapic, imazapyr, imazethapyr, imazamethabenz and imazaquinine, which are part of the Clearfield cropping system [1]. Phenolic compounds found in daily diets have various significant effects on diseases and experimental data are gathering regarding phenolic compounds as natural phytochemical antioxidants important for human health. Momordica charantia also called as bitter melon and kugua is widely cultivated in China, East Africa and South America. This plant has been traditionally used in folk medicine due to its an extensive range of nutritive and pharmacological properties against many diseases. Momordica has major chemical constituents, which are triterpenoids and their glycosides. A growing body of scientific literature has revealed that triterpenoids from Momordica are associated with their free-radical scavenging activity [2]. Pycnogenol (PYC), a family of flavonoids extracted from French maritime pine bark (Pinus pinaster Aiton, synonym Pinus maritima Mill.), which consisting of several types of phenolic compounds, condensed flavonoids and phenolic acids. It has been reported to have diverse beneficial pharmacological effects such as potent antioxidants, ROS scavenging and anti-inflammatory properties [3]. In this study we aimed that investigation of protective effect of pycnogenol and momardica on induced imazamox toxicity on L929 fibroblast cell line.

2. Material and Methods

Cell Culture: L929 fibroblast cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) (Gibco Sigma, St. Louis, MO, USA) supplemented with 10% fetal bovine serum (FBS; Invitrogen, Carlsbad, CA, USA), 100 IU/mL penicillin and 100 μg/mL of streptomycin in 75 cm2 culture flasks. Cells were maintained in a humidified atmosphere with 5% CO2 at 37 °C with medium renewal 2–3 times a week depending on cell density. Determination of Cell Viability: The viability of fibroblast cell was examined by using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay on the microplate reader (Gibco Sigma, St. Louis, MO, USA). Different concentration of imazamox (250 μM), momordica and pycnogenol (10−1–10−5 concentration) was applied on L929 fibroblast cells line for 24 h [4]. TAC and TOS: Spectrophotometric analysis was used for estimation of oxidative stress levels. Total oxidant status and TAC levels were measured after 24 h exposure to treatments. The cell mediums were collected when the experiments were completed. According to the manufacture procedure, TOS (H2O2 Equiv/mmol L-1) absorbance were evaluated at 530 nm and TAC (Trolox Equiv/mmol L-1) at 660 nm was evaluated (Rel assay, Antep, Turkey) [5,6]. Statistically Analysis: The statistical analysis was done by Mann–Whitney U test by using the SPSS 22.0 software (IBM company, Turkey). p < 0.05 was considered as statistically important distinction for whole test.

3. Results

MTT test: To determine cell viability, MTT assay was performed after 24 h exposure of imazamox, momordica and pycnogenol for fibroblast cell culture. (Figure 1).
According to our study pycnogenol high dose showned protective effect whereas momordica low dose showned protective effect p < 0.05. TAC and TOS: In current study pycnogenol increased TAC capacity in high dose but in lower dose pycnogenol did not show any promise (p < 0.05). Momordica results showed correlation with MTT result. According to this analyses momordica only in low dose increased antioxidant capacity and in addition, only in low dose TOS level were decreased (p > 0.05). (Figure 2).

4. Discussion

In conclusion momordica and pycnogenol effectively can be used in greenhouse worker toxicity. There is need to future study in laboratory animals to study chronic toxicity exposure of imazamox. In the present study, moderate necrotic and degenerative changes were detected in 250 µM imazamox reported that both technical grade imazamox [7] as well as an 11.83% formulation of this herbicide caused a slight erythema on the skin [8]. This data has correlation with our data fibroblast degeneration was seen in high dose of imazamox herbicide. In addition, our result show momordica and pycnogenol in possible toxicity can effectively protects skin cels and reduced oxidation status.

Author Contributions

A.T. designed the experiments; A.T. and B.C. performed the experiments; A.T. analyzed the data; A.T. and B.C. wrote the paper.

Acknowledgments

All sources of funding of the study were met by the authors.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Dabrowski, J.M.; Shadung, J.M.; Wepener, V. Prioritizing agricultural pesticides used in South Africa based on their environmental mobility and potential human health effects. Environ Int. 2014, 62, 31–40. [Google Scholar] [CrossRef] [PubMed]
  2. He, Q.; Li, Y.; Li, H.; Zhang, P.; Zhang, A. Hypolipidemic and antioxidant potential of bitter gourd (Momordica charantia L.) leaf in mice fed on a high-fat diet. Pak. J. Pharm. Sci. 2018, 31, 118–128. [Google Scholar]
  3. Packer, L.; Rimbach, G.; Virgili, F. Antioxidant activity and biologic properties of a procyanidin-rich extract from pine (Pinus maritima) bark, pycnogenol. Free Radic. Biol. Med. 1999, 27, 704–724. [Google Scholar] [CrossRef]
  4. Taghizadehghalehjoughi, A.; Hacimuftuoglu, A.; Cetin, M.; Ugur, A.B.; Galateanu, B.; Mezhuev, Y.; Okkay, U.; Taspinar, N.; Taspinar, M.; Uyanik, A.; et al. Effect of metformin/irinotecan-loaded poly-lactic-co-glycolic acid nanoparticles on glioblastoma: In vitro and in vivo studies. Nanomedicine 2018, 13, 1595–1606. [Google Scholar] [CrossRef] [PubMed]
  5. Erel, O. A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation. Clin Biochem. 2004, 37, 277–285. [Google Scholar] [CrossRef]
  6. Erel, O. A new automated colorimetric method for measuring total oxidant status. Clin Biochem. 2005, 38, 1103–1111. [Google Scholar] [CrossRef] [PubMed]
  7. Fischer, J. Skin Irritation Study in Albino Rabbits with AC 299,263 Technical: Lab Project Number: T-0519; New Jersey; American Cyanamid Co.: Wayne, NJ, USA, 1992. [Google Scholar]
  8. Boczon, L. Skin Irritation Study in Albino Rabbits with AC 299,263 1AS Formulation: Lab Project Number: T-0645: A 94-10; New Jersey; American Cyanamid Co.: Wayne, NJ, USA, 1994. [Google Scholar]
Figure 1. In vitro viability ratio of pycnogenol and momordica protective effect on induced imazamox toxicity effect on fibroblast cells (n = 6/group) were shown. * Significant differences at p < 0.05 compared to control group; ** Significant differences at the p < 0.001 compared to control group.
Figure 1. In vitro viability ratio of pycnogenol and momordica protective effect on induced imazamox toxicity effect on fibroblast cells (n = 6/group) were shown. * Significant differences at p < 0.05 compared to control group; ** Significant differences at the p < 0.001 compared to control group.
Proceedings 02 01584 g001
Figure 2. TAC and TOS of pycnogenol and momordica protective effect on induced imazamox toxicity effect on fibroblast cells (n = 6/group) were shown. * Significant differences at p < 0.05 compared to control group; ** Significant differences at the p < 0.001 compared to control group.
Figure 2. TAC and TOS of pycnogenol and momordica protective effect on induced imazamox toxicity effect on fibroblast cells (n = 6/group) were shown. * Significant differences at p < 0.05 compared to control group; ** Significant differences at the p < 0.001 compared to control group.
Proceedings 02 01584 g002
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Taghizadehghalehjoughi, A.; Cicek, B. Momordica and Pycnogenol Can Tolerate Imazamox Induced Toxicity in L929 Cells Line: In Vitro Study. Proceedings 2018, 2, 1584. https://doi.org/10.3390/proceedings2251584

AMA Style

Taghizadehghalehjoughi A, Cicek B. Momordica and Pycnogenol Can Tolerate Imazamox Induced Toxicity in L929 Cells Line: In Vitro Study. Proceedings. 2018; 2(25):1584. https://doi.org/10.3390/proceedings2251584

Chicago/Turabian Style

Taghizadehghalehjoughi, Ali, and Betul Cicek. 2018. "Momordica and Pycnogenol Can Tolerate Imazamox Induced Toxicity in L929 Cells Line: In Vitro Study" Proceedings 2, no. 25: 1584. https://doi.org/10.3390/proceedings2251584

APA Style

Taghizadehghalehjoughi, A., & Cicek, B. (2018). Momordica and Pycnogenol Can Tolerate Imazamox Induced Toxicity in L929 Cells Line: In Vitro Study. Proceedings, 2(25), 1584. https://doi.org/10.3390/proceedings2251584

Article Metrics

Back to TopTop