Jacob L S, Tallarida R J
Arch Int Pharmacodyn Ther. 1977 Jan;225(1):166-76.
Isolated rabbit thoracic aorta which is pharmacologically contracted will relax when exposed to ultraviolet light. The relaxation is reversible in that the tension is restored when the light source is removed. The purpose of this investigation was to study further the phenomenon of photorelaxation on vascular smooth muscle. Restoration kinetics were examined for two cases: 1) norepinephrine alone 2) norepinephrine plus phenoxylbenzamine. The photo-induced relaxation in the presence of the irreversible blocker phenoxybenzamine produced a more rapid restoration than the photo-induced relaxation in strips contracted with norepinephrine alone. Angiotensin, which is not blocked by phenoxybenzamine, produced no change in the restoration characteristics of a perturbation on the angiotensin-induced contractions. Strips treated with glycerin, a process which removes storage sites for Ca++, are responsive to exogenous administration of Ca++ but demonstrate no photorelaxation. These results lend supportive evidence to the hypothesis that ultraviolet radiation interferes with the drug-receptor complex.
药理学收缩的离体兔胸主动脉在暴露于紫外线时会松弛。这种松弛是可逆的,即当光源移除时张力会恢复。本研究的目的是进一步研究血管平滑肌的光松弛现象。对两种情况的恢复动力学进行了检查:1)单独使用去甲肾上腺素 2)去甲肾上腺素加酚苄明。在存在不可逆阻滞剂酚苄明的情况下,光诱导的松弛比单独用去甲肾上腺素收缩的条带中的光诱导松弛产生更快的恢复。血管紧张素不受酚苄明的阻断,对血管紧张素诱导的收缩的扰动的恢复特性没有影响。用甘油处理的条带,这一过程会去除钙离子的储存位点,对外源性钙离子给药有反应,但没有光松弛现象。这些结果为紫外线辐射干扰药物 - 受体复合物这一假说提供了支持性证据。