Tianjin Medical Journal ›› 2023, Vol. 51 ›› Issue (11): 1187-1192.doi: 10.11958/20230110

• Experimental Research • Previous Articles     Next Articles

Influence of miR-139-5p on cognitive dysfunction in rats with chronic cerebral hypoperfusion by targeting RIPK1/RIPK3/MLKL signal pathway

SHI Wenqian(), ZHAO Meiying, HUANG Jie, HE Gui, WANG Guiqing()   

  1. Department of Geriatrics, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, China
  • Received:2023-02-01 Revised:2023-03-29 Published:2023-11-15 Online:2023-11-07
  • Contact: E-mail:b0517012200@126.com

Abstract:

Objective To investigate the influence of miR-139-5p on cognitive dysfunction in chronic cerebral hypoperfusion (CCH) rats by targeting receptor-interacting protein kinase-1 (RIPK1)/receptor-interacting protein kinase-3 (RIPK3)/mixed lineage kinase domain-like protein (MLKL) signal pathway. Methods Sixty SPF SD rats were randomly divided into the sham operation group, the model group, the miR-NC group, the miR-139-5p mimic group and the miR-139-5p mimic+RIPK1 inhibitor Nec-1 group (miR-139-5p mimic+Nec-1 group), with 12 rats in each group. Except the sham group, the other groups used permanent ligation of bilateral common carotid arteries to construct rat CCH model. New object recognition experiment and Morris water maze were used to evaluate the cognitive function of rats. Enzyme linked immunosorbent assay (ELISA) was used to detect levels of glutathione peroxidase (GSH-Px), superoxide dismutase (SOD), malondialdehyde (MDA), inflammatory factor tumor necrosis factor (TNF)-α and interleukin-6 (IL-6) in rat hippocampus. Real-time quantitative PCR (qPCR) was used to detect the expression of miR-139-5p, RIPK1, RIPK3, MLKL mRNA in rat hippocampus. Western blot method was used to detect the protein expression levels of RIPK1, RIPK3, MLKL, synaptophysin (SYP), postsynaptic density protein 95 (PSD95) and α-synuclein (α-SYN). Double luciferase reporter gene experiment was used to verify the relationship between miR-139-5p and RIPK1. Results Compared with the sham group, the resolution coefficient, target quadrant residence time, levels of miR-139-5p, GSH-Px, SOD and the protein expression levels of SYP and PSD95 decreased obviously in hippocampus of the model group rats (P<0.05). The escape latency extended, and levels of MDA, TNF-α and IL-6 in hippocampus increased. The mRNA and protein expression of RIPK1, RIPK2, MLKL, the protein expression of α-SYN increased obviously (P<0.05). Compared with the model group and the miR-NC group, the expression trends of related indexes were opposite to the above in the miR-139-5p mimic group (P<0.05). Nec-1 further promoted the recovery of cognitive function in CCH rats by up-regulating the expression of miR-139-5p (P<0.05). MiR-139-5p negatively regulated the expression of RIPK1. Conclusion The up regulation of miR-139-5p may alleviate the cognitive dysfunction of CCH rats by targeting the inhibition of RIPK1/RIPK3/MLKL signaling pathway.

Key words: cognitive dysfunction, RIPK1/RIPK3/MLKL pathway, MicroRNA-139-5p, chronic cerebral hypoperfusion

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