Comparative regulation of ?1-adrenergic receptor mediated contraction in urogenitally derived smooth muscle
Autor: | P. Drescher, Dieter Rauch, Paul O. Madsen, F. Pereira, James A. Will |
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Rok vydání: | 1997 |
Předmět: |
Male
medicine.medical_specialty Time Factors Contraction (grammar) Urology Urogenital System In Vitro Techniques Contractility Phenylephrine Renal Artery Vas Deferens Prostate Epidermal growth factor Internal medicine medicine Animals Humans Receptor Dose-Response Relationship Drug Epidermal Growth Factor business.industry Vas deferens Muscle Smooth medicine.anatomical_structure Endocrinology Rabbits medicine.symptom business Muscle Contraction medicine.drug Muscle contraction |
Zdroj: | Urological Research. 25:S13-S19 |
ISSN: | 1434-0879 0300-5623 |
DOI: | 10.1007/bf00942042 |
Popis: | Contractility of smooth muscle within mammalian urogenital organ systems has an established role in physiological/pathophysiological functioning of the component structures. Our aim was to examine the direct effect of epidermal growth factor (EGF) on smooth muscle tone as well as its indirect effects in regulating alpha1-adrenoceptor-mediated contraction of the prostate, the vas deferens and renal arteries. Tissues were mounted isometrically, under controlled conditions, and changes in tension in response to treatment with phenylephrine (PE) with or without pretreatment with EGF were recorded on a physiological recorder via force transducers. In the rabbit prostate, EGF potentiated the magnitude of contraction to PE. The potentiation appeared to be dependent on cyclo-oxygenase products. In the human prostate, EGF potentiated the contractile response to PE. EGF had no effect on the PE-induced contraction of the rabbit renal artery and vas deferens. EGF alone did not alter smooth muscle tone in any of the above-mentioned tissues. The main finding of this study is the difference in the regulation by EGF of the alpha1-adrenoceptor-mediated response in smooth muscle of the prostate, from that by the vas deferens and renal artery. The reasons for this difference in response remain to be elucidated. This study may form the basis for further investigation into receptor transregulation and its relevance to symptomatic benign prostatic hyperplasia (BPH). |
Databáze: | OpenAIRE |
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