Bagrov Ia Iu, Manusova N B, Mozhaeva M G, Ostretsova I B, Antipenko A E, Diatlov R V
Fiziol Zh Im I M Sechenova. 1993 Oct;79(10):46-54.
Furosemide increased the hydrosmotic water flow in the frog urinary bladder and promoted the ADH-like effect of inhibitors of phosphodiesterase cAMP, potentiated hydrosmotic effects of theophylline and serosal osmotic hypertonicity but failed to change the effect of pituitrin. Fur reversibly suppressed oxytocin-induced contractions in the rat myometrium, inhibited the activity of the frog urinary bladder PDE cAMP, whereas the activity of the enzyme from the rat medulla and myometrium was activated by saluretic. Incubation of the myometrium strips in Fur resulted in a decrease in the cAMP content of the tissue. The cAMP seems to play an important role both in the myometrium smooth muscle relaxation and in the oxytocin-activated contractions.
呋塞米增加了蛙膀胱的水渗透性水流,并增强了磷酸二酯酶环磷酸腺苷(cAMP)抑制剂的抗利尿激素样作用,增强了茶碱和浆膜渗透压过高的水渗透性作用,但未能改变垂体后叶素的作用。呋塞米可逆性地抑制大鼠子宫肌层中催产素诱导的收缩,抑制蛙膀胱PDE cAMP的活性,而大鼠髓质和子宫肌层中该酶的活性则被促尿钠排泄剂激活。将子宫肌层条带在呋塞米中孵育会导致组织中cAMP含量降低。cAMP似乎在子宫肌层平滑肌松弛和催产素激活的收缩中都起着重要作用。