Department of Microbiology and Immunology, Faculty of Pharmacy, Damanhour University, Damanhour, 22511, Egypt.
Biochemistry Department, Faculty of Pharmacy, Delta University for Science and Technology, Gamasa, 11152, Egypt.
Eur J Pharmacol. 2022 Sep 15;931:175172. doi: 10.1016/j.ejphar.2022.175172. Epub 2022 Aug 6.
Diabetic cardiomyopathy is diagnosed by the development of abnormality in the structure and performance of myocardium in diabetic mellitus (DM) patients. Recent studies reported the association between altered gut microbiota and metabolic disorders like diabetes and cardiovascular diseases. Here, we aimed to investigate the gut-heart axis in an experimental animal model where we developed a novel therapeutic combination of dapagliflozin, crocin prebiotic and Lactobacilli probiotic to correct induced diabetic cardiomyopathy.
Diabetes mellitus was induced by Intraperitoneal (i.p) streptozotocin in male rats. The experimental design includes the administration of the tested drugs (Crocin, Dapagliflozin) solely and with Lactobacillus, or in combination therapy with and without Lactobacillus to the diabetic rats for six weeks. Clinical and microscopic evaluation scoring for cardiac tissues were determined. Biochemical markers including blood glucose level, adiponectin, resistin, cardiac injury markers, lipid profile, antioxidant enzymes, pro and anti-inflammatory markers were assessed. In addition, quantitative relative expression of PPARγ and TXINP genes and capsase-3 levels were measured. The change in the microbiota abundance was investigated using real-time PCR.
This study demonstrated the synergistic effect of the triple combination; dapagliflozin, crocin prebiotic, and Lactobacillus fermentum and Lactobacillus delbrueckii probiotic in treating diabetic cardiomyopathy in rats. The triple combination significantly reduced the oxidative, inflammatory, apoptotic activities induced by streptozotocin STZ and helped in restoring the symbiotic gut microbiota.
It is worthy to perform this study in clinical trials as a primary step to include crocin and Lactobacilli in the therapeutic protocols of diabetic cardiomyopathy.
糖尿病性心肌病的诊断依据是糖尿病(DM)患者心肌结构和功能的异常。最近的研究报告称,肠道微生物群的改变与糖尿病和心血管疾病等代谢紊乱有关。在这里,我们旨在研究实验动物模型中的肠道-心脏轴,在该模型中,我们开发了达格列净、藏红花前体和乳杆菌益生菌的新型联合治疗方法,以纠正诱导的糖尿病性心肌病。
雄性大鼠通过腹腔内(i.p)链脲佐菌素诱导糖尿病。实验设计包括单独给予测试药物(藏红花、达格列净)和给予乳杆菌,或联合治疗和不联合乳杆菌给予糖尿病大鼠六周。确定心脏组织的临床和显微镜评估评分。评估生化标志物,包括血糖水平、脂联素、抵抗素、心脏损伤标志物、血脂谱、抗氧化酶、促炎和抗炎标志物。此外,还测量了 PPARγ 和 TXINP 基因的定量相对表达和 caspase-3 水平。使用实时 PCR 研究微生物群丰度的变化。
本研究表明,达格列净、藏红花前体和乳杆菌发酵乳杆菌和乳杆菌德氏乳杆菌益生菌三联组合在治疗大鼠糖尿病性心肌病方面具有协同作用。三联组合显著降低了链脲佐菌素 STZ 诱导的氧化、炎症、凋亡活性,并有助于恢复共生肠道微生物群。
作为在临床试验中进行这项研究的第一步,将藏红花和乳杆菌纳入糖尿病性心肌病的治疗方案是值得的。