Extracellular matrix remodelling in rat heart in an unpredictable chronic mild stress model associated with diabetes

IF 0.7 4区 生物学 Q4 BIOLOGY Indian journal of experimental biology Pub Date : 2023-07-31 DOI:10.56042/ijeb.v61i08.2286
Houcine Dab, S. Hamed, W. Hodroj, L. Zourgui
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Abstract

The coexistence of depression and diabetes is a serious challenge in cardiovascular disease. However, extracellular matrix (ECM) under stress model associated or not with diabetes remains unknown. This study aims to investigate the involvement of diabetes and unpredictable chronic mild stress (UCMS) on ECM remodelling. Rats were exposed to UCMS, diabetes or combined treatment. mRNA expression of matrix metalloproteinases (MMP-2 and MMP-9), plasminogen activator (t-PA) and inhibitor (PAI-1) was examined by Q-RT-PCR. ECM was determined by ELISA. MMP-2 and MMP-9 mRNA was lower in diabetes ( P <0.05). UCMS increased MMP-2 and MMP-9 compared to control and diabetic group. Compared to the control and diabetes groups, MMP-2 and MMP-9 mRNA was significantly increased in the combined treatment group. UCMS increased MMP-2 expression in the diabetic group ( P <0.01). Compared to control, gelatinase activity was higher in diabetes and UCMS ( P <0.05). Combined diabetes and UCMS significantly increased gelatinase activity compared to T2D and UCMS groups. Collagen, hydroxyproline and fibronectin content were significantly increased in diabetes and combined groups. UCMS combined with diabetes exacerbated diabetes-induced MMPs and fibronectin deposition. In conclusion, comorbidity between diabetes and UCMS may exacerbate ECM remodelling. These findings will be useful in understanding diabetes-induced cardiovascular disease.
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在与糖尿病相关的不可预测的慢性轻度应激模型中大鼠心脏的细胞外基质重塑
抑郁症和糖尿病并存是心血管疾病面临的严峻挑战。然而,细胞外基质(ECM)在应激模型下是否与糖尿病相关仍然未知。本研究旨在探讨糖尿病和不可预测的慢性轻度应激(UCMS)对ECM重塑的影响。大鼠暴露于UCMS、糖尿病或联合治疗。用Q-RT-PCR检测基质金属蛋白酶(MMP-2和MMP-9)、纤溶酶原激活剂(t-PA)和抑制剂(PAI-1)的mRNA表达。采用ELISA法测定ECM。糖尿病组MMP-2和MMP-9mRNA表达较对照组和糖尿病组明显降低(P<0.05)。与对照组和糖尿病组相比,联合治疗组MMP-2和MMP-9mRNA显著增加。UCMS增加了糖尿病组MMP-2的表达(P<0.01)。与对照组相比,糖尿病和UCMS的明胶酶活性更高(P<0.05)。与T2D和UCMS组相比,合并糖尿病和UCMS显著增加了明胶酶活性。糖尿病组和合并糖尿病组的胶原、羟脯氨酸和纤连蛋白含量显著增加。UCMS联合糖尿病加重了糖尿病诱导的MMPs和纤连蛋白沉积。总之,糖尿病和UCMS之间的共病可能会加剧ECM重塑。这些发现将有助于理解糖尿病引起的心血管疾病。
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来源期刊
CiteScore
1.57
自引率
33.30%
发文量
84
审稿时长
6 months
期刊介绍: This journal, started in 1963, publishes full papers, notes and reviews in cell biology, molecular biology, genetic engineering, endocrinology, reproductive biology, immunology, developmental biology, comparative physiology, radiation biology, chronobiology, microbiology, pharmacology, toxicology and other biological fields including instrumentation and methodology. The papers having experimental design involving alteration and/or manipulation in biological system(s) providing insight into their functioning are considered for publication. Studies involving higher animals, human beings and of clinical nature are not encouraged for publication in the journal.
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