Neuroscience and Inflammation Unit, Department of Physiology, College of Health Sciences, University of Ilorin, Ilorin, Kwara State, Nigeria.
Internal Medicine Department, Cardiology Unit, LAUTECH Teaching Hospital, Ogbomoso, Oyo State, Nigeria.
J Basic Clin Physiol Pharmacol. 2021 Mar 18;33(2):213-222. doi: 10.1515/jbcpp-2020-0282.
There has been increasing recognition of the significant relationship between the autonomic nervous system and cardiovascular sequel in diabetes mellitus (DM) patients. Diabetic cardiac autonomic neuropathy (DCAN) still poses a treatment challenge in the clinical settings despite several research interventions. This study was designed to investigate the effect of carvedilol on experimentally induced DCAN in type 2 DM rat model.
DCAN was induced in 42 Wistar rats using high fat diet (HFD) for eight weeks, thereafter streptozotocin (STZ) at 25 mg/kg daily for five days. DCAN features were then assessed using non-invasive time and frequency varying holter electrocardiogram (ECG), invasive biomarkers, cardiac histology and cardiac nerve density.
Carvedilol significantly ameliorated the effects of DCAN on noradrenaline (p=0.010) and advanced glycated end products (AGEs) (p<0.0001). Similarly, carvedilol reversed the reduction in levels of antioxidants, sorbitol dehydrogenase (SD) activity (p=0.009) nerve growth factors (p<0.0001) and choline acetyl-transferase (p=0.031) following DCAN induction. Furthermore, heart rate variability (HRV) indices which were also reduced with DCAN induction were also ameliorated by carvedilol. However, carvedilol had no significant effect on cardiac neuronal dystrophy and reduced cardiac nerve densities.
Carvedilol improves physiological HRV indices and biomarkers but not structural lesions. Early detection of DCAN and intervention with carvedilol may prevent progression of autonomic neurologic sequel.
越来越多的人认识到自主神经系统与糖尿病患者心血管后果之间存在显著关系。尽管进行了多项研究干预,糖尿病性心脏自主神经病变(DCAN)在临床实践中仍然是一个治疗挑战。本研究旨在探讨卡维地洛对 2 型糖尿病大鼠模型中实验性诱导的 DCAN 的影响。
使用高脂肪饮食(HFD)诱导 42 只 Wistar 大鼠 8 周,然后用 25mg/kg 的链脲佐菌素(STZ)每天连续 5 天诱导 DCAN。然后使用非侵入性时频变化动态心电图(ECG)、侵入性生物标志物、心脏组织学和心脏神经密度评估 DCAN 特征。
卡维地洛显著改善了 DCAN 对去甲肾上腺素(p=0.010)和晚期糖基化终产物(AGEs)(p<0.0001)的影响。同样,卡维地洛逆转了 DCAN 诱导后抗氧化剂、山梨醇脱氢酶(SD)活性(p=0.009)、神经生长因子(p<0.0001)和胆碱乙酰转移酶(p=0.031)水平的降低。此外,DCAN 诱导后也降低了心率变异性(HRV)指数,卡维地洛也改善了这些指数。然而,卡维地洛对心脏神经元病变和减少的心脏神经密度没有显著影响。
卡维地洛改善生理 HRV 指数和生物标志物,但不能改善结构病变。早期检测 DCAN 并使用卡维地洛干预可能会阻止自主神经病变的进展。