ASTROM A, SAMELIUS U
Br J Pharmacol Chemother. 1957 Dec;12(4):410-4. doi: 10.1111/j.1476-5381.1957.tb00157.x.
The vasoconstrictor action of 5-hydroxytryptamine (5-HT) in the human placental preparation is about 10 times stronger than that of adrenaline and is antagonized by anti-adrenaline compounds like phentolamine. Both 5-HT and adrenaline are antagonized by yohimbine and chlorpromazine. Specific and strong anti-5-HT action is demonstrated for lysergic acid diethylamide (LSD) and tryptamine. Both LSD and tryptamine in larger doses have a vasoconstrictor action. Mescaline has no certain modifying effect on the action of 5-HT, but itself causes vasoconstriction in large doses. The antihistamine drug phenbenzamine in histamine blocking doses abolishes the action of 5-HT in half the preparations tested. The ganglionic blocking agent trimetaphan in large doses antagonizes the action of 5-HT added subsequently, and also, to a lesser degree, the effect of adrenaline. Hexamethonium and tetraethylammonium bromides are ineffective in this preparation. No certain modifying action of reserpine on subsequently added 5-HT could be demonstrated, and the same was true for heparin even in very high concentrations.
5-羟色胺(5-HT)对人体胎盘制剂的血管收缩作用比肾上腺素强约10倍,且可被酚妥拉明等抗肾上腺素化合物所拮抗。5-HT和肾上腺素均可被育亨宾和氯丙嗪所拮抗。麦角酸二乙胺(LSD)和色胺对5-HT具有特异性且强效的拮抗作用。大剂量的LSD和色胺均具有血管收缩作用。三甲氧苯乙胺对5-HT的作用没有确切的调节作用,但大剂量时自身会引起血管收缩。组胺阻断剂量的抗组胺药苯苄胺在一半的受试制剂中可消除5-HT的作用。大剂量的神经节阻断剂阿方那特可拮抗随后添加的5-HT的作用,对肾上腺素的作用也有较小程度的拮抗。六甲铵和溴化四乙铵在此制剂中无效。未发现利血平对随后添加的5-HT有确切的调节作用,即使是高浓度的肝素也是如此。