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  2. MiR-34a ameliorates arterial blood flow in rats with lower limb arteriosclerosis obliterans via Sirt1 signaling pathway

MiR-34a ameliorates arterial blood flow in rats with lower limb arteriosclerosis obliterans via Sirt1 signaling pathway

  • Cell Mol Biol (Noisy-le-grand). 2024 Mar 31;70(3):248-253. doi: 10.14715/cmb/2024.70.3.37.
Tuo Xu 1 Changwei Zheng 2 Yongkang Wu 3 Zhengde Chen 4 Huilai Miao 5
Affiliations

Affiliations

  • 1 Department of General Surgery, The First Affiliated Hospital, Jinan University, Guangzhou, China. dr_001tuoxu@163.com.
  • 2 Department of Vascular and Thyroid Surgery, The Affiliated Hospital of Guangdong Medical University, Zhanjiang, China. changweixheng20200202@163.com.
  • 3 Department of Vascular and Thyroid Surgery, The Affiliated Hospital of Guangdong Medical University, Zhanjiang, China. dr_yongkangwu0809@163.com.
  • 4 Department of Vascular and Thyroid Surgery, The Affiliated Hospital of Guangdong Medical University, Zhanjiang, China. zhengde_chen9989@163.com.
  • 5 Department of General Surgery, The First Affiliated Hospital, Jinan University, Guangzhou, China. mhl113729173387@163.com.
Abstract

In this study, we investigated the impact of microRNA-34a (miR-34a) on lower limb arteriosclerosis obliterans in rats through the Sirtuin 1 (SIRT1) signaling pathway. Thirty-six Sprague-Dawley rats were divided into normal, model, and miR-34a mimics groups. Rats in the normal group were raised normally, while the model group underwent lower limb arteriosclerosis obliterans induction and received saline injections. The miR-34a mimics group also underwent arteriosclerosis obliterans modeling but received miR-34a mimics injections. Immunohistochemistry revealed significantly increased vascular endothelial growth factor (VEGF) expression in both model and miR-34a mimics groups compared to the normal group, with the miR-34a mimics group showing higher levels. Western blotting indicated elevated SIRT1 protein expression in both non-normal groups, with the miR-34a mimics group exhibiting significantly higher levels. Quantitative polymerase chain reaction (qPCR) demonstrated higher levels of miR-34a, VEGF mRNA, and SIRT1 mRNA in the model group compared to the normal group, but significantly lower levels than the miR-34a mimics group. Enzyme-linked immunosorbent assay (ELISA) showed increased VEGF content in the model group compared to the normal group but decreased compared to the miR-34a mimics group. Hemorrheological detection revealed a reduced PU index in both non-normal groups compared to the normal group, with a significant increase in the miR-34a mimics group compared to the model group. Overall, miR-34a upregulation enhanced VEGF expression in rat blood vessels, ameliorating arterial blood flow in lower limb arteriosclerosis obliterans through the SIRT1 signaling pathway.

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