Djokic T D, Nadel J A, Dusser D J, Sekizawa K, Graf P D, Borson D B
Cardiovascular Research Institute, University of California, San Francisco.
J Pharmacol Exp Ther. 1989 Jan;248(1):7-11.
To evaluate the role of airway neutral endopeptidase (NEP) in the regulation of contraction of airway smooth muscle in response to endogenous tachykinins, we studied the effects of the NEP inhibitor phosphoramidon on contractions of guinea pig bronchial smooth muscle strips induced by either electrical field stimulation (EFS) or by capsaicin. In the presence of atropine (10(-6) M), propranolol (10(-6) M), phentolamine (10(-5) M), indomethacin (10(-6) M) and pyrilamine (5 x 10(-6) M) EFS (biphasic; pulse width, 1.0 msec; frequency 0.5-5 Hz for 30 sec; intensity, 20 V) produced noncholinergic, nonadrenergic muscle contraction in a frequency-dependent fashion (P less than .001). Phosphoramidon potentiated the contractile responses to EFS (P less than .01). Leucine-thiorphan (10(-5) M), another NEP inhibitor, potentiated EFS-induced contraction in a similar fashion as phosphoramidon (186 and 182% of control, respectively; each comparison, P less than .025). Captopril, bestatin, leupeptin and physostigmine (each drug, 10(-5) M) were without effect (P greater than .5, N = 5). Capsaicin (1.5 x 10(-8) M) produced long-lasting atropine-resistant smooth muscle contraction, an effect potentiated by phosphoramidon (10(-5) M (P less than .001). Removal of the epithelium slightly but significantly (P less than .05) increased the contractile responses to capsaicin and to EFS at impulse frequencies of 2 and 5 Hz, and phosphoramidon substantially increased contractions in tissues without epithelium. The trachea, bronchi and lungs each contained significant NEP activity.(ABSTRACT TRUNCATED AT 250 WORDS)
为了评估气道中性内肽酶(NEP)在调节气道平滑肌对内源性速激肽反应的收缩中的作用,我们研究了NEP抑制剂磷酰胺素对电场刺激(EFS)或辣椒素诱导的豚鼠支气管平滑肌条收缩的影响。在存在阿托品(10⁻⁶ M)、普萘洛尔(10⁻⁶ M)、酚妥拉明(10⁻⁵ M)、吲哚美辛(10⁻⁶ M)和吡苄明(5×10⁻⁶ M)的情况下,EFS(双相;脉冲宽度,1.0毫秒;频率0.5 - 5赫兹,持续30秒;强度,20伏)以频率依赖性方式产生非胆碱能、非肾上腺素能肌肉收缩(P <.001)。磷酰胺素增强了对EFS的收缩反应(P <.01)。另一种NEP抑制剂亮氨酸-硫氧吗啡(10⁻⁵ M)以与磷酰胺素类似的方式增强了EFS诱导的收缩(分别为对照的186%和182%;每次比较,P <.025)。卡托普利、贝司他汀、亮抑酶肽和毒扁豆碱(每种药物,10⁻⁵ M)均无作用(P >.5,N = 5)。辣椒素(1.5×10⁻⁸ M)产生持久的阿托品抗性平滑肌收缩,该效应被磷酰胺素(10⁻⁵ M)增强(P <.001)。去除上皮细胞轻微但显著地(P <.05)增加了对辣椒素和2赫兹及5赫兹脉冲频率的EFS的收缩反应,并且磷酰胺素显著增加了无上皮组织的收缩。气管、支气管和肺均含有显著的NEP活性。(摘要截短于250字)