2008
DOI: 10.1016/j.prostaglandins.2007.10.003
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Mechanism whereby nitric oxide (NO) infused chronically intrauterine in ewes is antiluteolytic rather than being luteolytic

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Cited by 14 publications
(5 citation statements)
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“…NONOate) only stimulated PGRB mRNA expression on Days 6-10 of the oestrous cycle. These data are supported by those of Weems et al (2008), who reported that intrauterine administration of an NO donor in ewes prevented the decline in P4 secretion, whereas an NO synthase inhibitor did not affect luteolysis. NO activity also altered the PGE : PGF 2a ratio, most likely by inhibiting 9-keto-PGE 2 reductase-mediated conversion of PGE 2 to PGF 2a (Weems et al 2008) .…”
Section: Table 2 Summary Of Changes In the Mrna Expression Of Progessupporting
confidence: 82%
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“…NONOate) only stimulated PGRB mRNA expression on Days 6-10 of the oestrous cycle. These data are supported by those of Weems et al (2008), who reported that intrauterine administration of an NO donor in ewes prevented the decline in P4 secretion, whereas an NO synthase inhibitor did not affect luteolysis. NO activity also altered the PGE : PGF 2a ratio, most likely by inhibiting 9-keto-PGE 2 reductase-mediated conversion of PGE 2 to PGF 2a (Weems et al 2008) .…”
Section: Table 2 Summary Of Changes In the Mrna Expression Of Progessupporting
confidence: 82%
“…These data are supported by those of Weems et al (2008), who reported that intrauterine administration of an NO donor in ewes prevented the decline in P4 secretion, whereas an NO synthase inhibitor did not affect luteolysis. NO activity also altered the PGE : PGF 2a ratio, most likely by inhibiting 9-keto-PGE 2 reductase-mediated conversion of PGE 2 to PGF 2a (Weems et al 2008) . Thus, we assume that NO strengthens the impact of P4 in the cow uterus through stimulation of PGRB mRNA only, which indicates its luteotropic rather than luteolytic action.…”
Section: Table 2 Summary Of Changes In the Mrna Expression Of Progessupporting
confidence: 82%
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“…254 Responses of NO appeared to differ in regard to functional and structural regression. 272 That interpretation could fit with the conclusion that decreased NO contributed to structural luteal regression. 249 In contrast to reports that NO is luteolytic, uterine infusion of NO donors during days 8-18 of the ovine estrous cycle produced heavier corpora lutea, greater progesterone in the jugular vein, and a greater ratio of PGE 2 :PGF 2α in the inferior vena cava in ewes that received the NO donor.…”
Section: Physiological Control Systems and Governing Gonadal Functionmentioning
confidence: 81%
“…Nitric oxide donor (2S)-2-pentylbutanedioic acid (NONate) is a compound that regulates blood flow and stimulates PGF2α synthesis in a cow's CL [21]. It also exerts anti-luteolytic properties by inhibiting the 9-keto-PGE2 reductase, which converts PGE2 to PGF2a, as demonstrated in sheep endometrium [22]. Aminoglutethimide (AMG) inhibits enzymes such as the cholesterol side-chain cleavage enzyme (CYP11A1, P450scc) and aromatase (CYP19A1), thus inhibiting the entire process of steroidogenesis [23].…”
Section: Introductionmentioning
confidence: 99%