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The effects of perphenazine and bromocriptine on follicular dynamics and endocrine profiles in anestrous pony mares.

机译:奋乃静和溴隐亭对动情小马母马卵泡动力学和内分泌特征的影响。

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19 anoestrous pony mares were given daily intramuscular injections of perphenazine (a dopamine antagonist; 0.375 mg/kg body weight), 2-bromo-ergocriptine (a dopamine agonist; 0.08 mg/kg metabolic weight) or saline (controls). Treatment began on January 20, 1994 and continued until ovulation occurred. Mares were teased 3 times weekly with an intact stallion. The ovaries were palpated and imaged weekly using an ultrasonic B-mode unit until they had a follicle >=20 mm. At this time, the ovaries were palpated and imaged 4 times per week. Blood samples were obtained immediately prior to ultrasonic imaging for measurement of prolactin, FSH and oestradiol-17beta. Compared with control, perphenazine advanced the spring transitional period and subsequent ovulation by approximately 30 days; onset of oestrus behaviour also occurred earlier (27.5 vs. 42.1 days; P<0.01). The animals developed large follicles (>30 mm) earlier than bromocriptine-treated mares (47.0±8.8 vs. 88.1±8.2 days; P<0.01) or controls (67.3±8.8 days). Bromocriptine, but not perphenazine, decreased (P<0.05) plasma prolactin levels throughout the study. However, perphenazine increased (P<0.05) mean plasma prolactin concentration from day 31 to 60 of treatment. There was no difference in mean plasma FSH or oestradiol-17beta concentration between treatment groups.
机译:每天肌肉注射19例小马母马奋乃静(一种多巴胺拮抗剂; 0.375 mg / kg体重),2-溴麦角隐亭(一种多巴胺激动剂; 0.08 mg / kg代谢重量)或生理盐水(对照组)。治疗从1994年1月20日开始,一直持续到排卵发生为止。母马每周被逗弄3次,并有完整的种马。每周一次使用超声B型单元触诊卵巢并成像,直到它们的卵泡> = 20 mm。此时,触诊卵巢并每周成像4次。在超声成像之前立即获得血样,用于测量催乳激素,FSH和雌二醇-17beta。与对照组相比,奋乃静将春季过渡期和随后的排卵提前了约30天。发情行为的发作也较早发生(27.5 vs. 42.1天; P <0.01)。这些动物比经溴隐亭治疗的母马(47.0±8.8天对88.1±8.2天; P <0.01)或对照(67.3±8.8天)更早形成大卵泡(> 30毫米)。在整个研究过程中,溴隐亭(而非奋乃静)未降低血浆催乳素水平(P <0.05)。然而,奋乃静从治疗的第31天到60天增加了(P <0.05)平均血浆催乳素浓度。治疗组之间的平均血浆FSH或雌二醇-17β浓度无差异。

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