Patel P, Itoh H, Lederis K, Hollenberg M D
Department of Pharmacology and Therapeutics, Faculty of Medicine, University of Calgary, Alta., Canada.
Can J Physiol Pharmacol. 1988 Oct;66(10):1308-12. doi: 10.1139/y88-214.
To evaluate further the action of epidermal growth factor - urogastrone (EGF-URO) in smooth muscle systems, we examined the effect of the peptide on guinea pig tracheal strips. The cumulative addition of EGF-URO to the organ bath resulted in a concentration-dependent tonic contraction without tachyphylaxis. The half-maximal contraction was obtained at 13 +/- 3 ng/mL EGF-URO (2 nM). The maximum contraction at 100 ng/mL approached 60% of that induced by 1 microM histamine. No significant difference in the EGF-URO-induced contraction was observed in the presence or absence of a functional epithelium. Preincubation with 1 microM indomethacin for 20 min abolished the action of EGF-URO. The contractile effect of EGF-URO was not affected by yohimbine, propranolol, atropine, tetrodotoxin, and esculetin. However, mepacrine caused inhibition by 37 +/- 7% (mean +/- SEM for n = 3). Verapamil (10 microM) inhibited the EGF-induced response by 62 +/- 5% (mean +/- SEM for n = 4); the response was also absent in Ca-free (1 mM EGTA) buffer. However, the response was restored after the readdition of calcium. Our results suggest that EGF-URO can modulate tracheal smooth muscle contractility via a cyclooxygenase product and raise the possibility that EGF-URO might play a role in controlling pulmonary smooth muscle tone in vivo.
为了进一步评估表皮生长因子-尿抑胃素(EGF-URO)在平滑肌系统中的作用,我们检测了该肽对豚鼠气管条的影响。向器官浴槽中累积添加EGF-URO会导致浓度依赖性的强直性收缩,且无快速耐受性。在13±3 ng/mL EGF-URO(2 nM)时可获得半数最大收缩。100 ng/mL时的最大收缩接近1 μM组胺诱导收缩的60%。在有或无功能性上皮的情况下,EGF-URO诱导的收缩无显著差异。用1 μM吲哚美辛预孵育20分钟可消除EGF-URO的作用。EGF-URO的收缩作用不受育亨宾、普萘洛尔、阿托品、河豚毒素和七叶亭的影响。然而,米帕林引起37±7%的抑制(n = 3时的平均值±标准误)。维拉帕米(10 μM)抑制EGF诱导的反应达62±5%(n = 4时的平均值±标准误);在无钙(1 mM EGTA)缓冲液中也无反应。然而,重新添加钙后反应恢复。我们的结果表明,EGF-URO可通过环氧化酶产物调节气管平滑肌收缩力,并增加了EGF-URO可能在体内控制肺平滑肌张力中发挥作用的可能性。