Dave K C, Jindal M N, Kelkar V V, Trivedi H D
Br J Pharmacol. 1979 Jun;66(2):197-201. doi: 10.1111/j.1476-5381.1979.tb13665.x.
1 Isolated duodenum of the rat, exposed to ultraviolet (u.v.) light in the presence of NO2 ions, responded with reversible relaxation. 2 The photorelaxation response did not seem to involve any known receptor mechanisms and was independent of any ganglionic or neuronal influences. 3 Changes in the ionic environment of the tissue showed that NA+ and Ca2+ were essential for the photorelaxation. K+ depolarized-tissue did not show the photoresponse. 4 The presence of the metabolic inhibitors, iodoacetic acid, 2,4-dinitrophenol, sodium fluoride, sodium azide or potassium cyanide, abolished the photorelaxation response. 5 It is proposed that the photorelaxation of the tissue resulted from the liberation of metabolic energy following NO2 ion-dependent absorption of u.v. light energy, which in turn, interfered with the Na+ ion movement across the cell membrane.
将大鼠的离体十二指肠暴露于有NO2离子存在的紫外线下时,会产生可逆性舒张反应。
光舒张反应似乎不涉及任何已知的受体机制,且不受任何神经节或神经元影响。
组织离子环境的变化表明,Na+和Ca2+对光舒张反应至关重要。K+使组织去极化时未表现出光反应。
代谢抑制剂碘乙酸、2,4-二硝基苯酚、氟化钠、叠氮化钠或氰化钾的存在会消除光舒张反应。
有人提出,组织的光舒张反应是由于在NO2离子依赖吸收紫外光能后代谢能量的释放所致,而这反过来又干扰了Na+离子跨细胞膜的移动。