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细胞内钙拮抗剂HA 1004对豚鼠的抗支气管收缩活性。

Antibronchoconstrictor activity of the intracellular calcium antagonist HA 1004 in guinea pigs.

作者信息

Chapman R W, Tozzi S, Kreutner W

机构信息

Department of Allergy and Inflammation, Schering-Plough Corporation, Bloomfield, N.J.

出版信息

Pharmacology. 1988;37(3):187-94. doi: 10.1159/000138462.

DOI:10.1159/000138462
PMID:2906438
Abstract

HA 1004 is a calcium antagonist vasodilator that inhibits contraction in vascular smooth muscle and lowers arterial blood pressure. The effects of HA 1004 on guinea pig airway smooth muscle contraction were compared to the effects of the calcium antagonists, verapamil and nifedipine and the bronchodilator, albuterol. In vitro, HA 1004, verapamil, nifedipine and albuterol inhibited Ca2+-induced contractions of the depolarized guinea pig trachea. HA 1004 and albuterol also relaxed the basal tracheal tone, whereas verapamil and nifedipine were inactive. The bronchorelaxant activity of HA 1004 was not blocked by propranolol. In vivo, intravenous administration of HA 1004, verapamil, nifedipine and albuterol effectively blocked bronchoconstriction induced by intravenous histamine and methacholine. HA 1004 also reversed a histamine-induced bronchospasm, as did albuterol, verapamil and nifedipine. Intratracheal administration of HA 1004 and albuterol inhibited histamine-induced bronchoconstriction without effecting blood pressure, whereas intratracheal administration of verapamil and nifedipine caused a significant reduction of blood pressure at their pulmonary active doses. These results show that HA 1004 has the ability to relax airway smooth muscle, inhibit contractile responses in the guinea pig airways, and there is separation of its cardiovascular and pulmonary effects when HA 1004 is administered directly to the lungs. The results are discussed in terms of the regulatory enzymes and sources of calcium that are involved in airway smooth muscle contraction.

摘要

HA 1004是一种钙拮抗剂血管扩张剂,可抑制血管平滑肌收缩并降低动脉血压。将HA 1004对豚鼠气道平滑肌收缩的作用与钙拮抗剂维拉帕米和硝苯地平以及支气管扩张剂沙丁胺醇的作用进行了比较。在体外,HA 1004、维拉帕米、硝苯地平和沙丁胺醇均抑制去极化豚鼠气管的Ca2 +诱导的收缩。HA 1004和沙丁胺醇还可松弛气管基础张力,而维拉帕米和硝苯地平则无此作用。HA 1004的支气管舒张活性不受普萘洛尔的阻断。在体内,静脉注射HA 1004、维拉帕米、硝苯地平和沙丁胺醇可有效阻断静脉注射组胺和乙酰甲胆碱诱导的支气管收缩。HA 1004还可逆转组胺诱导的支气管痉挛,沙丁胺醇、维拉帕米和硝苯地平也有此作用。气管内给予HA 1004和沙丁胺醇可抑制组胺诱导的支气管收缩而不影响血压,而气管内给予维拉帕米和硝苯地平在其肺部有效剂量时可导致血压显著降低。这些结果表明,HA 1004具有松弛气道平滑肌、抑制豚鼠气道收缩反应的能力,并且当直接将HA 1004给予肺部时,其心血管和肺部作用是分离的。根据参与气道平滑肌收缩的调节酶和钙来源对结果进行了讨论。

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