Sayet I, Neuilly G, Mironneau J, Mironneau C
Laboratoire de Physiologie Cellulaire et Pharmacologie Moléculaire, Centre National de la Recherche Scientifique 1489, Université de Bordeaux II, France.
J Appl Physiol (1985). 1995 May;78(5):1882-8. doi: 10.1152/jappl.1995.78.5.1882.
Effects of hindlimb suspension, spaceflight, and venous occlusion were examined in isolated strips from rat vena cava by using both [3H]prazosin-binding and contraction responses evoked by norepinephrine. Sensitivity to norepinephrine was decreased without modification of the maximal contractile response. Furthermore, the high K(+)-induced contractions were not affected, suggesting that there was no interference with voltage-dependent Ca2+ channels. The sensitivity of the norepinephrine-induced contraction to prazosin was decreased, and Scatchard analysis of [3H]prazosin binding indicated an increase in the dissociation constant without variation in maximal binding capacity. A similar increase in the dissociation constant was obtained in control rats after pretreatment with 3 microM norepinephrine or 0.1 microM phorbol 12,13-dibutyrate to desensitize the protein kinase C. This effect was completely abolished in the presence of GF-109203X, a selective inhibitor of protein kinase C. Taken together, these data indicate that altered gravity conditions induce a desensitization of alpha 1B-adrenoceptors depending on increased protein kinase C activity. This effect can be mimicked by venous occlusion and may be responsible for reduced contractile responses to norepinephrine.
利用[3H]哌唑嗪结合以及去甲肾上腺素引发的收缩反应,在大鼠腔静脉分离条上研究了后肢悬吊、太空飞行和静脉阻塞的影响。对去甲肾上腺素的敏感性降低,但最大收缩反应未改变。此外,高钾诱导的收缩不受影响,这表明对电压依赖性钙通道没有干扰。去甲肾上腺素诱导的收缩对哌唑嗪的敏感性降低,[3H]哌唑嗪结合的Scatchard分析表明解离常数增加,而最大结合容量无变化。在用3 microM去甲肾上腺素或0.1 microM佛波醇12,13 - 二丁酸预处理以使蛋白激酶C脱敏的对照大鼠中,也获得了类似的解离常数增加。在存在蛋白激酶C的选择性抑制剂GF - 109203X的情况下,这种效应完全消除。综上所述,这些数据表明,重力条件改变会导致α1B - 肾上腺素能受体脱敏,这取决于蛋白激酶C活性的增加。这种效应可被静脉阻塞模拟,可能是对去甲肾上腺素收缩反应降低的原因。