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四种前列腺素类似物对南非大狒狒(Papio ursinus ursinus)的溶解作用比较。

Comparison of the lytic effects of four prostaglandin analogues in the chacma baboon (Papio ursinus ursinus).

作者信息

Rall H J, Zuurmond T J, Weidemann A

出版信息

Int J Fertil. 1979;24(1):21-6.

PMID:37175
Abstract

Six healthy, cycling female chacma baboons (Papio ursinus ursinus) were used to determine the luteolytic effects of four prostaglandin analogues. The compounds were administered according to a study design which made provision for adequate controls. Five to seven days following ovulation, venous blood was collected and the baboon given a single intramuscular injection of a compound at a recommended dose. Blood was then collected serially every 3 h for three samples and again at 24, 48, and 72 h to determine the continued effect of the prostaglandin analogues on corpus luteum production of progesterone. It was found that PGF2alpha-1,15-lactone, 11alpha(15S)-17-phenyl-18,19,20-trinor-ent-PGE2 methyl ester and 17-phenyl-18,19,20-trinor-PGF2alpha exhibited definite luteolytic potential in this species. Equivocal results were obtained with (15S)-15-methyl-PGF2Alpha THAM and its toxic qualities resulted in the demise of three animals.

摘要

选用6只健康的、处于发情期的雌性东非狒狒(Papio ursinus ursinus)来确定四种前列腺素类似物的溶黄体作用。根据一项设有充分对照的研究设计来施用这些化合物。排卵后5至7天,采集静脉血,然后给狒狒以推荐剂量单次肌内注射一种化合物。随后每3小时连续采集血样共三份,之后在24、48和72小时再次采血,以确定前列腺素类似物对黄体产生孕酮的持续作用。结果发现,PGF2α-1,15-内酯、11α(15S)-17-苯基-18,19,20-三降-ent-PGE2甲酯和17-苯基-18,19,20-三降-PGF2α在该物种中表现出明确的溶黄体潜力。(15S)-15-甲基-PGF2α THAM的结果不明确,其毒性导致三只动物死亡。

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Inhibition of the monkey corpus luteum with 15-methyl prostaglandins.用15-甲基前列腺素抑制猴黄体。
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