Lippmann W
Experientia. 1978 Apr 15;34(4):441-3. doi: 10.1007/BF01935914.
Alrestatin at 25-1 X 10(-4) M inhibited the accumulation of cyclic AMP induced by prostaglandin E2, but not theophylline, in the rat anterior pituitary in vitro. Somatostatin, at lower concentrations, inhibited both; maximal inhibition of the prostaglandin effect was greater with alrestatin. As cyclic AMP is considered to be a mediator in induced-hormonal release, it appears from the present findings that alrestatin may be of potential use in altering hormonal release.
在体外实验中,25 - 1×10⁻⁴M的阿勒他汀抑制了前列腺素E2诱导的大鼠垂体前叶中环状AMP的积累,但不抑制茶碱诱导的积累。较低浓度的生长抑素对两者都有抑制作用;阿勒他汀对前列腺素作用的最大抑制作用更强。由于环状AMP被认为是诱导激素释放的介质,从目前的研究结果来看,阿勒他汀可能在改变激素释放方面具有潜在用途。