Cell and Molecular Biology Lab, Institute of Zoology, University of the Punjab, Lahore, Pakistan.
Department of Zoology, University of Okara, Okara, Pakistan.
Mol Biol Rep. 2023 Sep;50(9):7145-7154. doi: 10.1007/s11033-023-08600-4. Epub 2023 Jul 5.
The current study was designed to highlight the effects of heterologous platelet-rich plasma (PRP) on deteriorated hepatic tissues and impaired glucose metabolism of alloxan-induced diabetic mice.
30 male mice were divided into a control (CG), PRP (PG), diabetic (DG), and two treated groups (T1G and T2G). PG was given PRP treatment (0.5 ml/kg body weight) twice a week for four weeks. DG, T1G and T2G were given alloxan (150 mg/kg) to induce diabetes. After confirmation, PRP treatment was given to T1G and T2G for two and four weeks respectively while DG was left untreated. Upon completion of the said experimental period, liver samples were taken for histological and gene expression analyses.
The study found that the liver tissue of the DG group showed signs of damage, including hepatocyte ballooning, sinusoid dilatation, and collagen deposition. However, these changes were significantly reduced in both T1G and T2G groups. The expression of several genes related to liver function was also affected, with upregulation of Fbp1 and Pklr, and downregulation of Pck1 in the DG group. PRP treatment restored Fbp1 expression and also increased the expression of glycolytic pathway genes Hk1 and Gck, as well as Wnt signalling pathway genes Wnt2, Wnt4, and Wnt9a in both treated groups.
Current study revealed that heterologous PRP may partly alleviate high glucose levels in diabetics possibly by mediating glucose metabolism via inhibition of Wnt signalling pathway.
本研究旨在强调异种富血小板血浆(PRP)对己烷诱导糖尿病小鼠受损肝组织和葡萄糖代谢受损的影响。
30 只雄性小鼠分为对照组(CG)、PRP 组(PG)、糖尿病组(DG)和两组治疗组(T1G 和 T2G)。PG 每周两次给予 PRP 治疗(0.5ml/kg 体重),共四周。DG、T1G 和 T2G 给予己烷(150mg/kg)诱导糖尿病。确认后,T1G 和 T2G 分别给予 PRP 治疗 2 周和 4 周,而 DG 则未给予治疗。完成上述实验期后,取肝组织进行组织学和基因表达分析。
研究发现,DG 组的肝组织显示出损伤迹象,包括肝细胞气球样变、窦扩张和胶原沉积。然而,这些变化在 T1G 和 T2G 组中均显著减少。与肝功能相关的几个基因的表达也受到影响,DG 组中 Fbp1 和 Pklr 上调,Pck1 下调。PRP 治疗恢复了 Fbp1 的表达,并增加了糖酵解途径基因 Hk1 和 Gck 以及 Wnt 信号通路基因 Wnt2、Wnt4 和 Wnt9a 在两组治疗组中的表达。
本研究表明,异种 PRP 可能通过抑制 Wnt 信号通路来部分缓解糖尿病患者的高血糖水平,可能通过调节葡萄糖代谢。