Significant myocardial pathology and increase of alpha 1-adrenergic receptor number affecting the arrhythmogenic condition in cases with ventricular tachycardia.

Heart and vessels. Supplement Pub Date : 1990-01-01
M Hasumi, M Hiroe, N Fujita, S Hasumi, T Toyosaki, H Nagao, S Hosoda, T Kasajima, M Sekiguchi
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Abstract

To study the pathogenesis of idiopathic ventricular tachycardia with left bundle branch block morphology (LBBB-VT), histopathological findings in 34 patients and adrenergic receptor (AR) density obtained by micro-autoradiography in 11 patients were analyzed, using endomyocardial biopsy samples. According to the ventricular volume, we divided the patients into 3 groups. Group A patients (n = 8) were diagnosed as having arrhythmogenic right ventricular dysplasia (ARVD) showing right ventricular enlargement, group B patients (n = 7) showed decreased left ventricular function and/or enlarged left ventricle, and group C (n = 19) included patients with idiopathic ventricular tachycardia (VT) without enlargement or dysfunction of either ventricle. Histologically, there was a high incidence of significant pathology showing myocardial hypertrophy, degeneration, abnormal branching, and interstitial fibrosis in all groups (group A, 100%; group B, 86%; group C, 56%). There was a higher incidence of fatty tissue infiltration in groups A (100%), B (71%), C (48%) than in the control groups. As for AR, specific grains of alpha 1- and beta-AR were 23.0, and 18.3 (grains/25 x 25 mm square) respectively, in patients with LBBB-VT. The number of alpha 1 grains in patients with LBBB-VT was apparently higher than in the control group, sick sinus syndrome (SSS; 11.2), and the beta-AR density in the LBBB-VT group was the same as in the control group (SSS; 15.4). We concluded that the significant pathology in cases with VT might affect the arrhythmogenic condition. Moreover, these results suggested that the increase in the number of alpha 1-AR might have a great influence in idiopathic VT.

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室性心动过速心肌病理及α 1-肾上腺素能受体数目增加对致心律失常的影响。
为探讨特发性室性心动过速左束支阻滞形态(LBBB-VT)的发病机制,本文采用心内膜活检标本,对34例患者的组织病理表现和11例患者的显微放射自显影结果进行分析。根据心室容积将患者分为3组。A组患者(n = 8)诊断为心律失常性右室发育不良(ARVD),表现为右心室增大,B组患者(n = 7)表现为左心室功能下降和/或左心室增大,C组患者(n = 19)为特发性室性心动过速(VT),两心室均无增大或功能障碍。组织学上,各组心肌肥大、变性、异常分支、间质纤维化的发生率均较高(a组,100%;B组,86%;C组,56%)。a组脂肪组织浸润率(100%)、B组(71%)、C组(48%)均高于对照组。对于AR, LBBB-VT患者α - 1-和β -AR特异性颗粒分别为23.0粒和18.3粒(粒/25 × 25 mm方)。LBBB-VT患者α - 1颗粒数量明显高于对照组,病窦综合征(SSS;11.2), LBBB-VT组β - ar密度与对照组相同(SSS;15.4)。我们认为,室性心动过速的显著病理变化可能影响心律失常的发生。此外,这些结果提示α 1-AR数量的增加可能对特发性VT有很大的影响。
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