期刊
CHINESE JOURNAL OF INTEGRATIVE MEDICINE
卷 28, 期 6, 页码 531-537出版社
SPRINGER
DOI: 10.1007/s11655-022-3307-3
关键词
non-alcoholic fatty liver disease; Shilajit; adipokines; cytokines; glucose; insulin; dietary supplement; Ayurvedic medicine
资金
- Kerman University of Medical Science, Kerman, Iran
This study aimed to evaluate the effect of Shilajit, an Ayurvedic medicine, on the serum changes in cytokines and adipokines caused by non-alcoholic fatty liver disease (NAFLD). The results showed that Shilajit can protect against NAFLD by modulating the levels of cytokines and adipokines, reducing insulin resistance, and improving blood glucose levels.
Objective To evaluate the effect of Shilajit, a medicine of Ayurveda, on the serum changes in cytokines and adipokines caused by non-alcoholic fatty liver disease (NAFLD). Methods After establishing fatty liver models by feeding a high-fat diet (HFD) for 12 weeks, 35 Wistar male rats were randomly divided into 5 groups, including control (standard diet), Veh (HFD + vehicle), high-dose Shilajit [H-Sh, HFD + 250 mg/(kg center dot d) Shilajit], low-dose Shilajit [L-Sh, HFD + 150 mg/(kg center dot d) Shilajit], and pioglitazone [HFD + 10 mg/(kg center dot d) pioglitazone] groups, 7 rats in each group. After 2-week of gavage administration, serum levels of glucose, insulin, interleukin 1beta (IL-1 beta), IL-6, IL-10, tumor necrosis factor-alpha (TNF-alpha), adiponectin, and resistin were measured, and insulin resistance index (HOMA-IR) was calculated. Results After NAFLD induction, the serum level of IL-10 significantly increased and serum IL-1 beta, TNF-alpha levels significantly decreased by injection of both doses of Shilajit and pioglitazone (P<0.05). Increases in serum glucose level and homeostasis model of HOMA-IR were reduced by L-Sh and H-Sh treatment in NAFLD rats (P<0.05). Both doses of Shilajit increased adiponectin and decreased serum resistin levels (P<0.05). Conclusion The probable protective role of Shilajit in NAFLD model rats may be via modulating the serum levels of IL-1 beta, TNF-alpha, IL-10, adipokine and resistin, and reducing of HOMA-IR.
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