Weems Y S, Lennon E, Uchima T, Raney A, Goto K, Ong A, Zaleski H, Weems C W
Department of Human Nutrition, Food, and Animal Sciences, University of Hawaii, Honolulu, HI 96822, USA.
Prostaglandins Other Lipid Mediat. 2005 Dec;78(1-4):129-38. doi: 10.1016/j.prostaglandins.2005.06.002. Epub 2005 Jul 14.
Nitric oxide (NO) has been reported to be luteolytic based on treatment of cows in vivo with an inhibitor of nitric oxide synthase (NOS-produces NO), which delayed the decline in progesterone by two to three days [Jaroszewki J, Hansel, W. Intraluteal administration of a nitric oxide synthase blocker stimulates progesterone, oxytocin secretion and prolongs the life span of the bovine corpus luteum. Proc Soc Exptl Biol Med 2000;224:50-5; Skarzynski D, Jaroszewki J, Bah, M, et al. Administration of nitric oxide synthase inhibitor counteracts prostaglandin F(2alpha)-induced luteolysis in cattle. Biol Reprod 2003;68:1674-81]. The objective of this experiment was to determine the effect of a long acting NO donor or a NOS inhibitor infused chronically into the interstitial tissue of the ovarian vascular pedicle adjacent to the ovary with a corpus luteum on secretion of progesterone during the ovine estrous cycle. Ewes were treated either with Vehicle (N=5); Diethylenetriamine (DETA-control for DETA-NONOate; N=5); (Z)-1-[2-(2-aminoethyl)-N-(2-ammonioethyl) amino]diazen-1-ium-1,2-diolate (DETA-NONOate-long acting NO donor; N=6); or l-nitro-arginine methyl ester (l-NAME-NOS inhibitor; N=6) every 6 h from 24:00 h (0 h) on day 8 through 18:00 h on day 18 of the estrous cycle. Jugular venous blood was collected every 6h for analysis for progesterone and corpora lutea were collected at 18:00 h on day 18 and weighed. Weights of corpora lutea were heavier (P< or =0.05) in DETA-NONOate-treated ewes when compared to Vehicle, DETA, or l-NAME-treated ewes, which did not differ amongst each other (P> or =0.05). Profiles of progesterone in jugular venous blood on days 8-18 differed (P< or =0.05) in DETA-NONOate-treated ewes when compared to Vehicle, DETA, or l-NAME-treated ewes did not differ (P> or =0.05) amongst each other. It is concluded that NO is not luteolytic during the ovine estrous cycle, but may instead be antiluteolytic and prevent luteolysis.
据报道,一氧化氮(NO)具有溶黄体作用,这是基于在体内用一氧化氮合酶抑制剂(产生NO的NOS)处理奶牛的实验得出的,该抑制剂使孕酮下降延迟了两到三天[Jaroszewki J,Hansel,W。黄体内注射一氧化氮合酶阻滞剂可刺激孕酮、催产素分泌,并延长牛黄体的寿命。实验生物学与医学协会会刊2000;224:50 - 5;Skarzynski D,Jaroszewki J,Bah,M等。一氧化氮合酶抑制剂的给药可抵消前列腺素F(2α)诱导的牛黄体溶解。生物繁殖2003;68:1674 - 81]。本实验的目的是确定在绵羊发情周期中,将长效NO供体或NOS抑制剂长期注入与有黄体的卵巢相邻的卵巢血管蒂间质组织中,对孕酮分泌的影响。母羊分别接受以下处理:溶剂(N = 5);二亚乙基三胺(DETA - DETA - NONOate的对照;N = 5);(Z)-1 - [2 - (2 - 氨基乙基)-N - (2 - 氨乙基)氨基]重氮-1,2 - 二醇盐(DETA - NONOate - 长效NO供体;N = 6);或L - 硝基精氨酸甲酯(L - NAME - NOS抑制剂;N = 6),从发情周期第8天的24:00 h(0 h)开始,每6小时一次,直至第18天的18:00 h。每6小时采集颈静脉血用于分析孕酮,并在第18天的18:00 h采集黄体并称重。与接受溶剂、DETA或L - NAME处理的母羊相比,接受DETA - NONOate处理的母羊的黄体重量更重(P≤0.05),而接受溶剂、DETA或L - NAME处理的母羊之间没有差异(P≥0.05)。与接受溶剂、DETA或L - NAME处理的母羊相比(它们之间没有差异,P≥0.05),接受DETA - NONOate处理的母羊在第8 - 18天的颈静脉血中孕酮水平不同(P≤0.05)。结论是,在绵羊发情周期中,NO不是溶黄体的,而是可能具有抗溶黄体作用并防止黄体溶解。