毒蕈碱乙酰胆碱受体
自身抗体
内科学
内分泌学
受体
毒蕈碱乙酰胆碱受体M2
毒蕈碱乙酰胆碱受体M3
乙酰胆碱
心房颤动
下调和上调
乙酰胆碱受体
医学
化学
生物
抗体
免疫学
生物化学
基因
作者
Chang Ming Hong,Qiang Sun Zheng,Xiong Tao Liu,Fu Shang,Hongtao Wang,Wen Jiang
出处
期刊:Cardiology
[S. Karger AG]
日期:2008-07-31
卷期号:112 (3): 180-187
被引量:35
摘要
Evidence has shown that autoantibodies against M2 muscarinic acetylcholine receptors may play a role in the development of atrial fibrillation. The goal of this study was to evaluate the effects of anti-M2 receptor autoantibodies on rabbit atria in vivo.Rabbits were immunized monthly with a synthetic peptide corresponding to the M2 receptor. The atrial electrophysiology of the isolated perfused rabbit hearts was studied. Western blots and RT-PCR were performed to determine the expression of the atrial muscarinic receptor and the acetylcholine-activated potassium channel. Atrial tissue was stained with Masson's trichrome stain for fibrosis detection.Autoantibodies were persistently detected in immunized rabbits. M2 rabbits showed a significantly shorter atrial effective refractory period and a longer intra-atrial activation time than control rabbits. Electrical stimuli induced a significantly larger number of repetitive atrial responses in M2 rabbits. The protein levels of the M2 receptor and GIRK4 were upregulated in M2 rabbits. The mRNA levels of GIRK1 and GIRK4 were also upregulated. Histological examination revealed significantly increased diffuse fibrotic deposition in M2 rabbit atria compared with control rabbits.The M2 receptor autoantibody-positive rabbits showed altered atrial electrophysiology, overexpression of the M2 receptor-I(K,ACh) pathway and atrial fibrosis, which indicates that the autoantibodies against M2 receptors may participate in the induction and perpetuation of atrial fibrillation.
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