藏红花水提取物对亚慢性应激大鼠血糖调节以及肝Agt和TNF-α基因表达的影响

Advanced Biomedical Research Pub Date : 2023-05-15 eCollection Date: 2023-01-01 DOI:10.4103/abr.abr_51_22
Yeganeh Yazdani, Maryam Radahmadi, Roshanak Roustazade
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摘要

背景:压力和藏红花似乎以不同的方式影响血糖调节机制和胰岛素抵抗。研究了藏红花水提取物对亚慢性应激状态下大鼠血清葡萄糖水平、血清胰岛素水平、β细胞功能稳态模型评估(HOMA-B)、胰岛素抵抗稳态模型评估(HOMA-IR)、肾上腺重量、肝脏血管紧张素原(Agt)和肿瘤坏死因子-α(TNF-α)基因表达的影响:将42只雄性大鼠分为6组:对照组、束缚应激组(每天6小时,共7天)、藏红花(30和60 mg/kg)处理组(共7天)和应激后藏红花(30和60 mg/kg)处理组(共7天)。对血糖和胰岛素水平、肝脏 Agt 和 TNF-α 基因表达、HOMA-IR、HOMA-B 和肾上腺重量进行了测量:结果:亚慢性应激一周恢复后,高血糖、高胰岛素血症和胰岛素抵抗并不明显。该组肝脏 Agt 和 TNF-α mRNA 水平显著升高。服用藏红花可增强非应激受试者的肝脏 Agt mRNA。此外,应激-藏红花组的血清葡萄糖水平、胰岛素抵抗和肝脏 Agt 基因表达均显著增加。只有应激藏红花 60 组的肝脏 TNF-α 基因表达有所降低:结论:亚慢性应激后的藏红花治疗不仅没有改善糖耐量,反而增强了胰岛素抵抗。结论:亚慢性应激后使用藏红花治疗不仅不能改善糖耐量,反而会增强胰岛素抵抗,这表明藏红花和亚慢性应激在促进肾素-血管紧张素系统活性方面存在相互作用。此外,藏红花还能降低亚慢性应激后 TNF-α 基因的表达。藏红花和亚慢性应激对肝Agt基因表达的协同刺激作用导致了胰岛素抵抗和高血糖。
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Effects of Aqueous Saffron Extract on Glucoregulation as Well as Hepatic Agt and TNF-α Gene Expression in Rats Subjected to Sub-Chronic Stress.

Background: Stress and saffron seem to affect glucoregulation mechanisms and insulin resistance in different ways. Impacts of the aqueous saffron extract were investigated on serum glucose levels, serum insulin levels, the homeostatic model assessment of β-cell function (HOMA-B), the homeostatic model assessment of insulin resistance (HOMA-IR), adrenal weight, and hepatic gene expression of angiotensinogen (Agt) and tumor necrosis factor-α (TNF-α) in rats under sub-chronic stress.

Materials and methods: Forty-two male rats were divided into six groups: control, restraint stress (6h/day for seven days), saffron (30 and 60 mg/kg) treatments for seven days, and post-stress saffron (30 and 60 mg/kg) treatments for seven days. The serum glucose and insulin levels, hepatic gene expressions of Agt and TNF-α, HOMA-IR, HOMA-B, and adrenal gland weight were measured.

Results: One-week recovery following sub-chronic stress led to non-significant hyperglycemia, hyperinsulinemia, and insulin resistance. The hepatic Agt and TNF-α mRNA levels increased significantly in this group. Saffron administration led to enhanced hepatic Agt mRNA in the non-stressed subjects. In addition, serum glucose levels, insulin resistance, and hepatic Agt gene expression significantly increased in stress-saffron groups. The hepatic TNF-α gene expression was reduced only in the stress-saffron 60 group.

Conclusion: Saffron treatment after sub-chronic stress not only did not improve glucose tolerance but also enhanced insulin resistance. It indicated the interaction of saffron and sub-chronic stress to promote renin-angiotensin system activity. In addition, the saffron treatment decreased TNF-α gene expression after sub-chronic stress. The synergistic stimulating effect of saffron and sub-chronic stress on gene expression of hepatic Agt led to insulin resistance and hyperglycemia.

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