Startseite Anti-nociceptive and anti-inflammatory effects of Withania somnifera root in fructose fed male rats
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Anti-nociceptive and anti-inflammatory effects of Withania somnifera root in fructose fed male rats

  • Mohammad Reza Shahraki , Zahra Samadi Noshahr EMAIL logo , Hassan Ahmadvand und Alireza Nakhaie
Veröffentlicht/Copyright: 6. Juli 2016

Abstract

Background: Insulin resistance is a metabolic disorder which affects the diabetes mellitus pathophysiology and alters the cell excitability. This study has been designed to evaluate the anti-nociceptive and anti-inflammatory effects of chronic administration of Withania somnifera root (WSR) in fructose drinking water rats.

Methods: An experiment was carried out on 48 Wistar-Albino male rats, weighting 200±30 g, which were divided into six groups (n=8): control group (C), control morphine (CM), W. somnifera group (WS) which received WSR (62.5 mg/g diet), W. somnifera naloxone group (WSN) which received WSR and naloxone, fructose (F) group which received fructose drinking water and FWS group which received fructose-enriched drinking water and WSR during the trial period. A biphasic pain response was induced after intraplantar injection of formalin (50 μL, 1%). Pain behavior was measured using Dubuisson methods. The obtained data were analyzed by SPSS software V. 18, using ANOVA and Tukey test. Results were expressed as mean±SD. Statistical differences were considered significant at p<0.05.

Results: The results showed that the insulin resistance index, blood sugar, insulin, IL-6, TNF-α, and acute and chronic pain score in the F group were significantly increased in comparison with the control group, but these parameters in the FWS group were significantly decreased compared with the F group (p<0.001).

Conclusions: Our findings indicated that chronic oral administration of WSR has analgesic and anti-inflammatory effects in fructose drinking water rats and causes improved insulin resistance index.

Acknowledgments

We are grateful to Dr. Mahnaz Shahrakipour for his kind cooperation.

  1. Author contributions: Shahraki, Samadi, Ahmadvand and Alireza Nakhaie developed the original idea and protocol, collected and analyzed data and wrote the manuscript. All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This study was financially supported by the Deputy Research center at Zahedan University of Medical Sciences.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

1. Di Lorenzo C, Dell’agli M, Colombo E, Sangiovanni E, Restani P. Metabolic syndrome and inflammation: a critical review of in vitro and clinical approaches for benefit assessment of plant food supplements. Evid Based Complement Alternat Med 2013;2013:782461.10.1155/2013/782461Suche in Google Scholar

2. Onat A. Metabolic syndrome: nature, therapeutic solutions and options. Expert Opin Pharmacother 2011;12:1887–900.10.1517/14656566.2011.585462Suche in Google Scholar

3. Bray GA, Nielsen SJ, Popkin BM. Consumption of high-fructose corn syrup in beverages may play a role in the epidemic of obesity. Am J Clin Nutr 2004;79:537–43.10.1093/ajcn/79.4.537Suche in Google Scholar

4. Mamikutty N, Thent ZC, Sapri SR, Sahruddin NN, Mohd Yusof MR, Haji Suhaimi F. The establishment of metabolic syndrome model by induction of fructose drinking water in male Wistar rats. Biomed Res Int 2014;2014:263897.10.1155/2014/263897Suche in Google Scholar

5. Tobey T, Mondon C, Zavaroni I, Reaven G. Mechanism of insulin resistance in fructose-fed rats. Metabolism 1982;31:608–12.10.1016/0026-0495(82)90100-7Suche in Google Scholar

6. Xu H, Barnes GT, Yang Q, Tan G, Yang D, Chou CJ, et al. Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance. J Clin Invest 2003;112:1821–30.10.1172/JCI200319451Suche in Google Scholar

7. Mozaffari-Khosravi H, Ahadi Z, Fallah Tafti M. The effect of green tea versus sour tea on insulin resistance, lipids profiles and oxidative stress in patients with type 2 diabetes mellitus: a randomized clinical trial. Iran J Med Sci 2014;39:424–32.Suche in Google Scholar

8. Bal Y, Adas M, Helvaci A. Evaluation of the relationship between insulin resistance and plasma tumor necrosis factor-alpha, interleukin-6 and C-reactive protein levels in obese women. Bratisl Lek Listy 2010;111:200–4.Suche in Google Scholar

9. Slangen R, Schaper NC, Faber CG, Joosten EA, Dirksen CD, van Dongen RT, et al. Spinal cord stimulation and pain relief in painful diabetic peripheral neuropathy: a prospective two-center randomized controlled trial. Diabetes Care 2014;37:3016–24.10.2337/dc14-0684Suche in Google Scholar PubMed

10. Anwer T, Sharma M, Pillai KK, Iqbal M. Effect of Withania somnifera on insulin sensitivity in non-insulin-dependent diabetes mellitus rats. Basic Clin Pharmacol Toxicol 2008;102:498–503.10.1111/j.1742-7843.2008.00223.xSuche in Google Scholar PubMed

11. Gupta GL, Rana A. Withania somnifera (Ashwagandha): a review. Pharmacogn Rev 2007;1:129.Suche in Google Scholar

12. Shukla K, Dikshit P, Shukla R, Sharma S, Gambhir JK. Hypolipidemic and antioxidant activity of aqueous extract of fruit of Withania coagulans (Stocks) Dunal in cholesterol-fed hyperlipidemic rabbit model. Indian J Exp Biol 2014;52:870–5.Suche in Google Scholar

13. Peana AT, Muggironi G, Spina L, Rosas M, Kasture SB, Cotti E, et al. Effects of Withania somnifera on oral ethanol self-administration in rats. Behav Pharmacol 2014;25:618–28.10.1097/FBP.0000000000000078Suche in Google Scholar PubMed

14. Kyathanahalli CN, Manjunath MJ, Muralidhara. Oral supplementation of standardized extract of Withania somnifera protects against diabetes-induced testicular oxidative impairments in prepubertal rats. Protoplasma 2014;251:1021–9.10.1007/s00709-014-0612-5Suche in Google Scholar PubMed

15. Gupta A, Singh S. Evaluation of anti-inflammatory effect of Withania somnifera root on collagen-induced arthritis in rats. Pharm Biol 2014;52:308–20.10.3109/13880209.2013.835325Suche in Google Scholar

16. Siriwardane AS, Dharmadasa RM, Samarasinghe K. Distribution of Withaferin A, an anticancer potential agent, in different parts of two varieties of Withania somnifera (L.) Dunal. Grown in Sri Lanka. Pak J Biol Sci 2013;16:141–4.10.3923/pjbs.2013.141.144Suche in Google Scholar

17. Orrù A, Marchese G, Casu G, Casu MA, Kasture S, Cottiglia F, et al. Withania somnifera root extract prolongs analgesia and suppresses hyperalgesia in mice treated with morphine. Phytomedicine 2014;21:745–52.10.1016/j.phymed.2013.10.021Suche in Google Scholar

18. Prabu PC, Panchapakesan S, Raj CD. Acute and sub-acute oral toxicity assessment of the hydroalcoholic extract of Withania somnifera roots in Wistar rats. Phytother Res 2013;27:1169–78.10.1002/ptr.4854Suche in Google Scholar

19. Dubuisson D, Dennis SG. The formalin test: a quantitative study of the analgesic effects of morphine, meperidine, and brain stem stimulation in rats and cats. Pain 1978;4:161–74.10.1016/0304-3959(77)90130-0Suche in Google Scholar

20. Kujawska-Łuczak M, Suliburska J, Markuszewski L, Pupek-Musialik D, Jabłecka A, Bogdański P. The effect of L-arginine and ascorbic acid on the visceral fat and the concentrations of metalloproteinases 2 and 9 in high-fat-diet rats. Endokrynol Pol 2015;66:526–32.10.5603/EP.2015.0065Suche in Google Scholar PubMed

21. Lê KA, Tappy L. Metabolic effects of fructose. Curr Opin Clin Nutr Metab Care 2006;9:469–75.10.1097/01.mco.0000232910.61612.4dSuche in Google Scholar PubMed

22. Oudot C, Lajoix AD, Jover B, Rugale C. Dietary sodium restriction prevents kidney damage in high fructose-fed rats. Kidney Int 2013;83:674–83.10.1038/ki.2012.478Suche in Google Scholar PubMed

23. Gao Z, Leng S, Lu F, Xie M, Xu L, Wang K. Effect of berberine on expression of hepatocyte nuclear factor-4alpha in rats with fructose-induced insulin resistance. J Huazhong Univ Sci Technol Med Sci 2008;28:261–5.10.1007/s11596-008-0307-2Suche in Google Scholar PubMed

24. Ruiu S, Longoni R, Spina L, Orrù A, Cottiglia F, Collu M, et al. Withania somnifera prevents acquisition and expression of morphine-elicited conditioned place preference. Behav Pharmacol 2013;24:133–43.10.1097/FBP.0b013e32835f3d15Suche in Google Scholar PubMed

25. Veličković N, Djordjevic A, Vasiljević A, Bursać B, Milutinović DV, Matić G. Tissue-specific regulation of inflammation by macrophage migration inhibitory factor and glucocorticoids in fructose-fed Wistar rats. Br J Nutr 2013;110:456–65.10.1017/S0007114512005193Suche in Google Scholar PubMed

26. Nosálová G, Sivová V, Ray B, Fraňová S, Ondrejka I, Flešková D. Antitussive activity of Withania somnifera and opioid receptors. Adv Exp Med Biol 2015;838:19–25.10.1007/5584_2014_79Suche in Google Scholar PubMed

27. Gupta A, Singh S. Evaluation of anti-inflammatory effect of Withania somnifera root on collagen-induced arthritis in rats. Pharm Biol 2014;52:308–20.10.3109/13880209.2013.835325Suche in Google Scholar PubMed

28. Ahmadvand H. Amelioration of altered antioxidant enzyme activity by Satureja khuzestanica essential oil in alloxan-induced diabetic rats. Chin J Nat Med 2014;12:672–6.10.1016/S1875-5364(14)60102-3Suche in Google Scholar

29. Ahmadvand H, Ghasemi-Dehnoo M. Antiatherogenic, hepatoprotective, and hypolipidemic effects of coenzyme Q10 in alloxan-induced type 1 diabetic rats. ARYA Atheroscler 2014;10:192–8.10.1016/S2222-1808(14)60481-3Suche in Google Scholar

30. Udayakumar R, Kasthurirengan S, Vasudevan A, Mariashibu TS, Rayan JJ, Choi CW, et al. Antioxidant effect of dietary supplement Withania somnifera L. reduces blood glucose levels in alloxan-induced diabetic rats. Plant Foods Hum Nutr 2010;65:91–8.10.1007/s11130-009-0146-8Suche in Google Scholar PubMed

31. Oh JH, Kwon TK. Withaferin A inhibits tumor necrosis factor-alpha-induced expression of cell adhesion molecules by inactivation of Akt and NF-kappaB in human pulmonary epithelial cells. Int Immunopharmacol 2009;9:614–9.10.1016/j.intimp.2009.02.002Suche in Google Scholar PubMed

Received: 2015-5-22
Accepted: 2016-1-30
Published Online: 2016-7-6
Published in Print: 2016-6-1

©2016 by De Gruyter

Artikel in diesem Heft

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  2. Reviews
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  5. Oxidative Stress
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