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Hypoglycemic and hypolipidemic effect of pentaamino acid fullerene C60 derivative in rats with metabolic disorderстатья
- Авторы: Soldatova Yu V., Areshidze D.A., Kozlova M.A., Zhilenkov A.V., Kraevaya O.A., Faingold I.I., Troshin P.A., Kotelnikova R.A.
- Журнал: Journal of Bioenergetics and Biomembranes
- Год издания: 2023
- Издательство: Springer/Plenum Publishers
- Местоположение издательства: New York, USA
- DOI: 10.1007/s10863-023-09961-y
- Аннотация: link -https://link.springer.com/article/10.1007/s10863-023-09961-yPentaamino acid fullerene C60 derivative is a promising nanomaterial, which exhibited antihyperglycemic activity in high-fat diet and streptozotocin-induced diabetic rats. This study investigates the effect of pentaaminoacid C60 derivative (PFD) in rats with metabolic disorders. Rats were assigned to 3 groups (of 10 rats each) as follows: Group 1 (normal control), group 2 included the protamine-sulfate-treated rats (the untreated group of animals with the model metabolic disorder); group 3 (Protamine sulfate + PFD) included the protamine-sulfate-treated model rats that received an intraperitoneal injection of PFD. Metabolic disorder in rats was initiated by protamine sulfate (PS) administration. The PS + PFD group was injected intraperitoneally with PFD solution (3 mg/kg). Protamine sulfate induces biochemical changes (hyperglycemia, hypercholesterolemia, and hypertriglyceridemia) in the blood and morphological lesions in rat liver and pancreas. The potassium salt of fullerenylpenta-N-dihydroxytyrosine in protamine sulfate-induced rats normalized blood glucose level and the serum lipid profile and improved hepatic function markers. Treatment with PFD restored pancreas islets and liver structure of protamine sulfate-induced rats compared to the untreated group. PFD is a promising compound for further study as a drug against metabolic disorders.
- Добавил в систему: Солдатова Юлия Валериевна