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喜来芝在调节非酒精性脂肪肝大鼠抵抗素、脂联素和细胞因子中的保护作用。

Protective Roles of Shilajit in Modulating Resistin, Adiponectin, and Cytokines in Rats with Non-alcoholic Fatty Liver Disease.

机构信息

Physiology Research Center, Kerman University of Medical Sciences, Kerman, 7616914115, Iran.

Endocrinology, and Metabolism Research Center, Kerman University of Medical Sciences, Kerman, 7616914115, Iran.

出版信息

Chin J Integr Med. 2022 Jun;28(6):531-537. doi: 10.1007/s11655-022-3307-3. Epub 2022 Mar 8.

DOI:10.1007/s11655-022-3307-3
PMID:35258780
Abstract

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·d) Shilajit], low-dose Shilajit [L-Sh, HFD + 150 mg/(kg·d) Shilajit], and pioglitazone [HFD + 10 mg/(kg·d) pioglitazone] groups, 7 rats in each group. After 2-week of gavage administration, serum levels of glucose, insulin, interleukin 1beta (IL-1β), IL-6, IL-10, tumor necrosis factor-alpha (TNF-α), 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-1β, TNF-α 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-1β, TNF-α, IL-10, adipokine and resistin, and reducing of HOMA-IR.

摘要

目的

评估希拉杰特(一种阿育吠陀药物)对非酒精性脂肪肝(NAFLD)引起的细胞因子和脂肪因子血清变化的影响。

方法

通过高脂饮食(HFD)喂养 12 周建立脂肪肝模型后,将 35 只雄性 Wistar 大鼠随机分为 5 组,包括对照组(标准饮食)、Veh 组(HFD+载体)、高剂量希拉杰特[H-Sh,HFD+250mg/(kg·d)希拉杰特]、低剂量希拉杰特[L-Sh,HFD+150mg/(kg·d)希拉杰特]和吡格列酮[HFD+10mg/(kg·d)吡格列酮]组,每组 7 只。灌胃 2 周后,测定血清葡萄糖、胰岛素、白细胞介素 1β(IL-1β)、IL-6、IL-10、肿瘤坏死因子-α(TNF-α)、脂联素和抵抗素水平,并计算胰岛素抵抗指数(HOMA-IR)。

结果

NAFLD 诱导后,两剂量希拉杰特和吡格列酮注射均可使血清 IL-10 水平显著升高,血清 IL-1β和 TNF-α水平显著降低(P<0.05)。L-Sh 和 H-Sh 治疗可降低 NAFLD 大鼠血清葡萄糖水平和 HOMA-IR 升高(P<0.05)。两剂量希拉杰特均可增加脂联素,降低血清抵抗素水平(P<0.05)。

结论

希拉杰特可能通过调节血清中 IL-1β、TNF-α、IL-10、脂联素和抵抗素水平,降低 HOMA-IR,在 NAFLD 模型大鼠中发挥保护作用。

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