Comparative Histopathologic Evaluation of the Effects of Portulaca oleracea, Omega-3, and Combination of Sodium Selenite and Vitamin E on Hepatic Enzymes of Experimental Diabetic Rats

Main Article Content

Ali Shabestari Asl
Alireza Sadeghi
Muhammad Saeed
Arman Moshavery

Abstract

Introduction: Portulaca oleracea (PO) plant, Omega 3, and Sodium Selenite plus Vitamin E exert antidiabetic effects by compensating for the deficiency in insulin release and enhancing antioxidant status. The purpose of the present study was to comparatively assess the effect of Portulaca oleracea, omega-3, and a combination of Sodium Selenite and Vitamin E on hepatic enzyme activities in streptozotocin-induced diabetic rats.


Materials and methods: A total of 48 adult male Wistar rats (weighing approximately 220 ± 10 g) were injected by a single intraperitoneal injection of streptozotocin (60 mg/kg body weight.) and were randomly assigned to 4 groups, and 4 replicates for each group. Group 1 served as diabetic control, groups 2, 3, and 4 received Portulaca oleracea extract (1.5 mg/kg/day, orally), Omega-3 (500 mg/kg/day, orally), and Sodium Selenite (0.5 mg/kg/day, orally) plus Vitamin E (400 Iu/kg/day, orally), respectively, for 28 days. At the end of the study, blood samples were taken for biochemical investigations.


Results: The levels of blood glucose, AST, ALP, and GGT enzymes in all treatment groups were less than those of the control group. The ALT enzyme activity in rats treated with Portulaca oleracea and Vitamin E plus Selenium was less than in control and omega-3 treatment groups.


Conclusion: Results indicated that Portulaca oleracea is more effective in hepatic enzyme activities of diabetic rats, compared to other treatment groups.

Article Details

How to Cite
Babazadeh, D., Shabestari Asl, A., Sadeghi, A., Saeed, M., & Moshavery, A. (2022). Comparative Histopathologic Evaluation of the Effects of Portulaca oleracea, Omega-3, and Combination of Sodium Selenite and Vitamin E on Hepatic Enzymes of Experimental Diabetic Rats. Small Animal Advances, 1(1), 4–9. https://doi.org/10.58803/saa.v1i1.2
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Original Articles

References

Abedimanesh N, Asghari, S, Mohammadnejad K, Daneshvar Z, Rahmani S, Shokoohi S, Farzaneh AH, Hosseini S H, Jafari Anarkooli I, Noubarani M et al. The anti-diabetic effects of betanin in streptozotocin-induced diabetic rats through modulating AMPK/SIRT1/NF-κB signaling pathway. Nutr Metab (Lond) 2021; 18: 92. DOI: https://doi.org/10.1186/s12986-021-00621-9

Ramakrishna V, and Jailkhani R. Evaluation of oxidative stress in Insulin Dependent Diabetes Mellitus (IDDM) patient. Diagnotice Pathology. 2007; 2: 22. DOI: https://www.doi.org/10.1186/1746-1596-2-22

Davi G, Falco A, and Patrono C. Lipid peroxidation in diabetes mellitus. Antioxidant and Redox Signal. 2005; 7: 256-268. DOI: https://www.doi.org/10.1089/ars.2005.7.256

Liu L, Howe P, Zhou YF, Xu ZQ, Hocart C, and Zhan R. Fatty acids and beta- carotene in australian purslane (Portulaca oleracea) varieties. J Chromatogr. 2000; 893: 127-132. DOI: https://www.doi.org/ 10.1016/s0021-9673(00)00747-0

Kalaivanam KN, Dharmalingam M, and Marcus SR. Lipid peroxidation in type 2 diabetes mellitus, Inter J Diabetes in Developing Countries. 2006; 26: 30-32. DOI: https://www.doi.org/10.4103/0973- 3930.26889

King GL, and Loeken MR. Hyperglycemiainduced oxidative stress in diabetic complications. Histochemistry and Cell biology. 2004; 122: 333- 338. DOI: https://www.doi.org/10.1007/s00418-004-0678-9

Sindhu RK, Koo JR, Roberts C.K, and Vaziri ND. Dysregulation of hepatic superoxide dismutase, catalase and glutathione peroxidase in diabetes: response to insulin and antioxidant therapies. Clin

and experimental hypertension. 2004; 38: 43-53. DOI: https://www.doi.org/10.1081/ceh-120027330

Yalçin O, Karataş F, Erulaş FA, and Ozdemir E. The levels of glutathione peroxidase, vitamin A, E, C and lipid peroxidation in patients with transitional cell carcinoma of the bladder. BJU Inter. 2004; 93: 863-866. DOI: https://www.doi.org/10.1111/j.1464-410X.2003.04729.x

Peerapatdit T, Patchanans N, Likidlilid A, Poldee S, and Sriratanasathavorn C. Plasma lipid peroxidation and antioxidiant nutrients in type 2 diabetic patients. J Med Association of Thailand. 2006; 89: 147-155. Available at: https://www.pubmed.ncbi.nlm.nih.gov/17718256/

Shrilatha B, and Muralidhara. Occurrence of oxidative impairments, response of antioxidant defences and associated biochemical perturbations in male reproductive milieu in the Streptozotocin diabetic rat. Inter J Andrology. 2007; 30: 508-518. DOI: https://www.doi.org/10.1111/j.1365-2605.2007.00748.x

Peuchant E, Brun JL, Rigalleau V, Dubourg L, Thomas MJ, Daniel JY, Leng JJ, and Gin H. Oxidative and antioxidative status in pregnant women with either gestational or type 1 diabetes. Clin Biochem. 2004; 37: 293- 298. DOI: https://www.doi.org/10.1016/j.clinbiochem.2003.12.005

Saravanan R, Viswana P, and Pugalendi KV. Protective effect of urosolic acid on ethanol-Mediated experimental liver damage

in rats. Life Sciences. 2006. 78: 713-718. DOI: https://www.doi.org/10.1016/j.lfs.2005.05.060

Enriquez R, Giri M, Rottiers R, and Christophe A. Fatty acid composition of erythrocyte phospholipids are related to insulin levels, secretion and resistance in obese type 2 diabetics on

Metformin. Clin Chem Acta. 2004; 346: 145-152. DOI: https://www.doi.org/10.1016/j.cccn.2004.02.029

Pasaoglu H, Sancak B, and Bukan N. Lipid peroxidation and resistance to oxidation in patients with type 2 diabetes mellitus, Tohoku J Exp Med. 2004; 203: 211-218. DOI: https://www.doi.org/10.1620/tjem.203.211

Al Shamsi M, Amin A, and Adeghate E. Beneficial effect of Vitamin E on the metabolic parameters of diabetic rats. Mol Cell Bio. 2004; 261: 35–42. DOI: https://www.doi.org/10.1023/b:mcbi.0000028735.79172.9b

Kinalski M, Sledziewski A, Telejko B, Zarzycki W, and Kinalska I. Lipid peroxidation and scavenging enzyme activity in streptozotocininduced diabetes. Acta Diabetol. 2000; 37: 179- 83. DOI: https://www.doi.org/10.1007/s005920070002

Traber MG, and Atkinson J. Vitamin E, antioxidant and nothing

more. Free Radical BioMed. 2007; 43: 4-15. DOI: https://www.doi.org/10.1016/j.freeradbiomed.2007.03.024

Hatfield DL, Berry MJ, and Gladyshev VN. Selenoproteins and selenoproteomes, second ed, New York, Springer. 2006; 99-110. DOI: https://www.doi.org/10.1007/0-387-33827-6_9

Barbosa NB, Rocha JB, Soares JC, Wondracek DC, Goncalves JF, Schetinger MR, and Nogueria CW. Dietary diphenyl diselenide reduces the STZ induced toxicity. Food Chem Toxicology. 2008; 46: 186-194. DOI: https://www.doi.org/10.1016/j.fct.2007.07.014

Erbayraktar Z, Yilmaz O, Artmann AT, Cehreli R, and Coker C. Effects of Selenium supplementation on antioxidant defense and glucose homeostasis in experimental diabetes mellitus. Bio Trace Element Res. 2007; 118: 217-226. DOI: https://www.doi.org/10.1007/s12011-007- 0037-5

Heydari M, Hashempur MH, Daneshfard B, and Mosavat SH. Bioactive Foods as Dietary Intervention for Diabetes Second ed.Bioactive Food as Dietary Interventions for Diabetes. 2019; 49-68 Available at: https://www.sciencedirect.com/topics/medicine-and-dentistry/ portulaca-oleracea

Zheng G, Mo F, Ling C, and et al. Portulaca oleracea L. alleviates liver injury in streptozotocin-induced diabetic mice. Drug Des Devel Ther. 2017;12: 47-55. DOI: https://www.doi.org/10.2147/DDDT.S121084

Gao D, wang Li Q and Fan Y. Hypoglycemic effects and mechanisms of Portulaca oleracea L. in alloxan-induced diabetic rats. J Med Plants Res. 2010; 4: 1996-2003 DOI: https://www.doi.org/10.5897/JMPR10.181

Mohamed-I Kotb, and El-Sayed. Effects of Portulaca oleracea L. seeds in treatment of type-2 diabetes mellitus patients as adjunctive and alternative therapy, J Ethnopharmacology. 2011; 137: 643-651 DOI: https://www.doi.org/10.1016/j.jep.2011.06.020

Abdullah M S and Kusumaningtyas R D. The extraction of purslane (Portulaca oleracea L.) using alcohol solvents 48 % and its utilization as a source of encapsulated omega-3 oil. AIP Conference Proceedings 2197, 080004. 2020 DOI: https://www.doi.org/10.1063/1.5140944

Duncan D B. Multiple range and multiple (F test) Biometrics.1955; 11: 1-42. DOI: https://doi.org/10.2307/3001478

Sachin L, Badole, Subhash L, and Bodhankar l. Interaction of aqueous extract of Pleurotus pulmonarius (Fr)Quel-Champ with acarbose in alloxan induced diabetic mice. J. Appl. Biomed. 2007; 5: 157–166. DOI: https://www.doi.org/10.32725/jab.2007.021

Ramadan BK, Schaalan MF, and Tolba AM. Hypoglycemic and pancreatic protective effects of Portulaca oleracea extract in alloxan induced diabetic rats. BMC Complement Altern Med. 2017; 17:37. DOI: https://www.doi.org/10.1186/s12906-016-1530-1

Samarghandian S, Borji A and Farkhondeh T. Attenuation of Oxidative Stress and Inflammation by Portulaca oleracea in Streptozotocin-Induced Diabetic Rats. J Evid Based Complementary Altern Med. 2017; 22 :562-566. DOI: https://doi.org/10.1177/2156587217692491

Dehghan F, Soori R, Gholami K, and et al. Purslane (Portulaca oleracea) Seed Consumption and Aerobic Training Improves Biomarkers Associated with Atherosclerosis in Women with

Type 2 Diabetes (T2D) Sci Rep. 2016; 6: 37819. DOI: https://www.doi.org/10.1038/srep37819

Parsa H, Shiravand T, Ranjbar K, and Komaki A. The Effect of Exercise Training and Portulaca oleracea on Neurobehavioral Dysfunction

in Type 2 Diabetic Rats. Researchsquare.com. 2021 DOI: https://www.doi.org/10.21203/rs.3.rs-630661/v1

Laurent L. Triple Action Purslane Extract for Healthy Blood Glucose Levels. 2009;Available at http://newhope360.com/botanicals/triple-action-purslane-extract-healthy-blood-glucose-levels.

Ezekwe MO, Omara-Alwala TR, and Membrahtu T. Nutritive characterization of purslane accessions as influenced by planting

date. Plant Foods Hum Nutr. 1999; 54: 183-191. DOI: https://www.doi.org/10.1023/a:1008101620382

Zargari A. Medical plants (in Persian). Fourth ed. Teh Uni Pub. 1990; 3: 130-132.

Hussein MA and Abdel-Gawad SM. In vivo hepato-protective properties of purslane extracts on paracetamol induced liver

damage. Malaysian J Nutr. 2010; 16: 161– 170. Available at: https://www.europepmc.org/article/med/22691863

Roozi H, Mashhadi M, Boojar A, Eidi A, and Khavari-Nejad R. The effect of Portulaca oleracea alkaloids on antidiabetic properties through changes in ceramide metabolism, Egyp J Basic and Applied Sci. 2021; 8: 156-166. DOI: https://www.doi.org/10.1080/2314808X.2021.1877889

Schuman M. Overview of purslane edible and medicinal herb. NNFA Today. 2001; 15: p. 12.

Blevs J, Navas-Acien A, and Guallar E. Serum Selenium and diabetes

in US adults, Diabetes Care. 2007; 30: 829- 834. DOI: https://www.doi.org/10.2337/dc06-1726

Jamilian M, and Ravanbakhsh N. Effects of Vitamin E plus Omega-3 Supplementation on Inflammatory Factors, Oxidative Stress Biomarkers and Pregnancy Consequences in Women with Gestational Diabetes. J Arak Uni Med Sci. 2018; 21: 32-41 Available at: http://www.jams.arakmu.ac.ir/article-1-5638-en.html

Baburao Jain A, and Anand Jain V. Vitamin E, Its Beneficial Role in Diabetes Mellitus (DM) and Its Complications. J Clin Diagn Res. 2012; 6: 1624-1628. DOI: https://www.doi.org/10.7860/JCDR/2012/4791.2625

Balbi ME, Tonin FS, Mendes AM and et al. Antioxidant effects of vitamins in type 2 diabetes: a meta-analysis of randomized controlled trials. Diabetol Metab Syndr. 2018; 10 :18. DOI: https:// www.doi.org/10.1186/s13098-018-0318-5

Thierry C, Gerbi A, Vague P, Pieroni G, Raccah D. Neuroprotective effect of docosahexaenoic acidenriched phospholipids in experimental diabetic neuropathy. Diabetes. 2003; 52: 2578-2585. DOI: https://www.doi.org/10.2337/diabetes.52.10.2578

Tabei SM, Fakher S, Djalali M, Javanbakht MH, Zarei M, Derakhshanian H, Sadeghi MR, Mostafavi E, and Kargar F. Effect of Vitamins A, E, C and omega-3 fatty acids supplementation on the level of catalase

and superoxide dismutase activities in streptozotocin-induced

diabetic rats. Bratisl Lek Listy. 2015; 116: 115-118. DOI: https://www.doi.org/10.4149/bll_2015_022

Naziroğlu M. Protective role of intraperitoneally administered Vitamin E and Selenium in rats anesthetized with enflurane. Biological Trace Element Research.1999; 69: 199-209. DOI:10.1007/BF02783872

Çay M and Naziroğlu M., Effects of intraperitoneally-administered Vitamin E and Selenium on the blood biochemical and haematological parameters in rats. Cell Biochemistry and Function. 1999; 17: 143–148. DOI: https://doi.org/10.1002/(SICI)1099-0844(199906)17:2<143 AID-CBF802>3.0.CO;2-H

Ali SI, Said MM, and Hassan EK. Prophylactic and curative effects of purslane on bile duct ligation-induced hepatic fibrosis in

albino rats. Ann Hepatol. 2011; 10: 340-346. Available at: https://pubmed.ncbi.nlm.nih.gov/21677337/

Ghahramani R, Eidi M, Ahmadian H, Hamidi Nomani M, Abbasi R, Alipour M and et al. Anti-diabetic Effect of Portulaca oleracea (Purslane) Seeds in Alloxan-induced Diabetic Rats. IJML. 2016; 3: 282-289. Available at: http://ijml.ssu.ac.ir/article-1-150-en.html

Zarei A, Changizi Ashtiyani S, and Taheri S. The effects of hydroalcoholic extract of Portulaca oleracea on the serum concentreation of Hepatic enzymes in Rats. Iran South Med J. 2014; 17: 889-899. Available at: http://ismj.bpums.ac.ir/article-1-603-en.html

Abdel Megeid AA, Attia Ael R, Elmarasy SS and Ibrahim AM. Effect of different types of fish on rats suffering from diabetes. J Nutr and Health. 2008 ;19 :257-271. DOI: https://doi.org/10.1177/026010600801900402

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