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Askari, Nahid, jafari, Elham, Bagheri-Hosseinabadi, Zahra, Amiri, Maryam, Khanamani Falahati-pour, Sakineh, Baghery, Fatemeh, Dini, Ali, Mirzaei, Vahid, Khanamani Falahati-pour, Soudeh. (1403). Amelioration of Diabetes and Nonalcoholic Fatty Liver Disease by Pistachio Kernel Protein Hydrolysate in Rats. سامانه مدیریت نشریات علمی, 13(4), 1129-1136. doi: 10.22034/jmpb.2024.364228.1630
Nahid Askari; Elham jafari; Zahra Bagheri-Hosseinabadi; Maryam Amiri; Sakineh Khanamani Falahati-pour; Fatemeh Baghery; Ali Dini; Vahid Mirzaei; Soudeh Khanamani Falahati-pour. "Amelioration of Diabetes and Nonalcoholic Fatty Liver Disease by Pistachio Kernel Protein Hydrolysate in Rats". سامانه مدیریت نشریات علمی, 13, 4, 1403, 1129-1136. doi: 10.22034/jmpb.2024.364228.1630
Askari, Nahid, jafari, Elham, Bagheri-Hosseinabadi, Zahra, Amiri, Maryam, Khanamani Falahati-pour, Sakineh, Baghery, Fatemeh, Dini, Ali, Mirzaei, Vahid, Khanamani Falahati-pour, Soudeh. (1403). 'Amelioration of Diabetes and Nonalcoholic Fatty Liver Disease by Pistachio Kernel Protein Hydrolysate in Rats', سامانه مدیریت نشریات علمی, 13(4), pp. 1129-1136. doi: 10.22034/jmpb.2024.364228.1630
Askari, Nahid, jafari, Elham, Bagheri-Hosseinabadi, Zahra, Amiri, Maryam, Khanamani Falahati-pour, Sakineh, Baghery, Fatemeh, Dini, Ali, Mirzaei, Vahid, Khanamani Falahati-pour, Soudeh. Amelioration of Diabetes and Nonalcoholic Fatty Liver Disease by Pistachio Kernel Protein Hydrolysate in Rats. سامانه مدیریت نشریات علمی, 1403; 13(4): 1129-1136. doi: 10.22034/jmpb.2024.364228.1630

Amelioration of Diabetes and Nonalcoholic Fatty Liver Disease by Pistachio Kernel Protein Hydrolysate in Rats

Journal of Medicinal plants and By-Products
مقاله 23، دوره 13، شماره 4، اسفند 2024، صفحه 1129-1136    اصل مقاله (892.38 K)
نوع مقاله: Research Paper
شناسه دیجیتال (DOI): 10.22034/jmpb.2024.364228.1630
نویسندگان
Nahid Askari1؛ Elham jafari2؛ Zahra Bagheri-Hosseinabadi3؛ Maryam Amiri4؛ Sakineh Khanamani Falahati-pour5؛ Fatemeh Baghery6؛ Ali Dini6؛ Vahid Mirzaei7، 8؛ Soudeh Khanamani Falahati-pour* 6
1Department of Biotechnology, Institute of Sciences and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, Iran
2Pathology and Stem Cell Research Center, Kerman University of Medical Sciences, Kerman, Iran
3Department of Clinical Biochemistry, Faculty of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
4Department of Medical Laboratory Science, Faculty of Paramedical Science, Jiroft University of Medical Sciences, Jiroft, Iran
5Department of Pharmacology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
6Pistachio Safety Research Center, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
7Clinical Research Development Unit, Ali-Ibn Abi-Talib Hospital, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
8Department of Internal Medicine, Faculty of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran
چکیده
Diabetes Mellitus (DM) and Nonalcoholic Fatty Liver Disease (NAFLD) are prevalent conditions that affect the metabolism and can lead to liver injury. They are often associated with obesity and insulin resistance. Protein Hydrolysate of Pistachio Kernel (PHPK) is a natural product obtained from pistachio proteins by enzymatic hydrolysis. It has been reported to have antioxidant, anti-inflammatory, and antidiabetic properties. We investigated the hepatoprotective effects of PHPK in rats with type 1 DM or NAFLD induced by a high-sugar diet. We used 96 male Wistar rats and divided them into four groups: Control, NAFLD, Diabetic, and PHPK-treated (5, 50, 500 mg/kg). We fed the rats with different diets for 8 weeks and then administered PHPK orally for 4 weeks. We collected blood and liver samples for biochemical and histopathological analysis. We found that DM and NAFLD increased the levels of liver enzymes, cholesterol, and triglycerides in the blood and caused hepatic damage, as shown by distorted liver architecture, necrotic hepatocytes, sinusoidal dilatation, and kupffer cell proliferation. PHPK administration reduced the severity of these alterations and improved the liver function and morphology in rats with DM and NAFLD. Our results suggest that PHPK has beneficial effects on DM and NAFLD, indicating its potential as a natural remedy for these disorders. Future research is needed to identify the specific compound(s) responsible for its antidiabetic effects and to elucidate its mechanism of action.
کلیدواژه‌ها
Diabetes Mellitus؛ Non-Alcoholic Fatty Liver Disease؛ Bioactive peptide؛ Pistacia
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