Balduini W, Costa L G
Department of Environmental Health, University of Washington, Seattle 98195.
Brain Res. 1990 Apr 2;512(2):248-52. doi: 10.1016/0006-8993(90)90633-M.
The in vitro effects of ethanol (EtOH) on muscarinic receptor-stimulated phosphoinositide metabolism were measured in cerebral cortex slices of adult and 7-day-old rats. EtOH (500 mM) caused a significant decrease (32-43%) of maximal accumulation of [3H]inositol phosphates (InsPs) induced by carbachol, and a 2-fold increase in its EC50 in 7-day-old rats, but had no effect in adult rats. The effect of EtOH on [3H]InsPs accumulation in neonatal rats was significant at a concentration as low as 150 mM. The inhibitory effect of EtOH was maximal in cerebral cortex and hippocampus and lower in cerebellum, while no effect was observed in the brainstem. While carbachol- and acetylcholine-stimulated phosphoinositide metabolism were inhibited by EtOH, EtOH had no effect on norepinephrine-, histamine-, and serotonin-stimulated phosphoinositide hydrolysis. These results are qualitatively and quantitively similar to those previously found following in vivo administration of EtOH to developing and to adult rats, suggesting that the muscarinic receptor-stimulated phosphoinositide metabolism might represent a target for EtOH-induced developmental neurotoxicity.
在成年大鼠和7日龄大鼠的大脑皮层切片中测定了乙醇(EtOH)对毒蕈碱受体刺激的磷酸肌醇代谢的体外影响。乙醇(500 mM)导致卡巴胆碱诱导的[3H]肌醇磷酸(InsPs)最大积累量显著降低(32 - 43%),并且在7日龄大鼠中其半数有效浓度(EC50)增加了2倍,但对成年大鼠没有影响。乙醇对新生大鼠[3H]InsPs积累的影响在低至150 mM的浓度时就很显著。乙醇的抑制作用在大脑皮层和海马中最大,在小脑中较低,而在脑干中未观察到影响。虽然卡巴胆碱和乙酰胆碱刺激的磷酸肌醇代谢受到乙醇抑制,但乙醇对去甲肾上腺素、组胺和5-羟色胺刺激的磷酸肌醇水解没有影响。这些结果在定性和定量上与先前对发育中的大鼠和成年大鼠进行乙醇体内给药后发现的结果相似,表明毒蕈碱受体刺激的磷酸肌醇代谢可能是乙醇诱导的发育性神经毒性的一个靶点。