Tsurumi K, Abe A, Fujimura H, Asai H, Nagasaka M
Nihon Yakurigaku Zasshi. 1976;72(1):41-52. doi: 10.1254/fpj.72.41.
PZ-177 was found to have potent analgesic, anti-inflammatory and mild central depressive actions. In the present work, the general pharmacological actions of PZ-177 were tested in order to investigate other significant actions and to determine the side effects. PZ-177 showed no significant pharmacological activities on the respiratory and cardiovascular system, on the renal function, on the autonomic nervous system, on the sugar level and coagulation in blood and on local irritation. Volume and acidity of gastric juice were decreased and turn over was not inhibited in the connective tissure. Thus PZ-177 was considered to have no ulcerogenic action on the gastric mucosa. The compound relaxed the tonus of isolated small intestine, tracheal muscles and uterus and stopped spontaneous movement. Moreover the contraction of those smooth muscles by such spasmogens as acetylcholine, histamine serotonin, BaCl2 and oxytocin was inhibited by PZ-177 and the activity was almost the same with each spasmogen. It was found therefore to have spasmolytic activity and no specific antagonistic action on the chemical mediators. PZ-177 showed also wear relaxant activity on the skeletal muscle. Those actions on the muscles may have a curative effect on inflammation in bronchotracheal and gastrointestinal tracts or on pain with contraction of skeletal muscle. From the above results, it may be considered that PZ-177 is a relatively safe and useful analgesic and anti-inflammatory compound.
发现PZ - 177具有强效镇痛、抗炎及轻度中枢抑制作用。在本研究中,对PZ - 177的一般药理作用进行了测试,以探究其他显著作用并确定其副作用。PZ - 177在呼吸和心血管系统、肾功能、自主神经系统、血糖水平及血液凝固和局部刺激方面未显示出明显的药理活性。胃液的量和酸度降低,结缔组织中的周转率未受抑制。因此,认为PZ - 177对胃黏膜无致溃疡作用。该化合物可使离体小肠、气管肌肉和子宫的张力松弛,并使自发运动停止。此外,PZ - 177可抑制乙酰胆碱、组胺、血清素、氯化钡和催产素等致痉剂引起的这些平滑肌收缩,且对每种致痉剂的活性几乎相同。因此发现它具有解痉活性,对化学介质无特异性拮抗作用。PZ - 177对骨骼肌也显示出松弛活性。这些对肌肉的作用可能对支气管气管和胃肠道炎症或骨骼肌收缩引起的疼痛具有治疗作用。从上述结果来看,可认为PZ - 177是一种相对安全且有用的镇痛和抗炎化合物。