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给雌性大鼠注射性激素或促性腺激素释放激素后,垂体自体移植于肾被膜下时促性腺细胞的维持情况。

Maintenance of gonadotrophs in pituitary autografts under the kidney capsules of female rats given sex hormones or LRH.

作者信息

Shino M, Fujihara N, Rennels E G

出版信息

Am J Anat. 1980 Aug;158(4):433-444. doi: 10.1002/aja.1001580405.

Abstract

Female Sprague-Dawley rats were hypophysectomized and the anterior pituitary gland was immediately placed under the kidney capsule. For 1 week after surgery, groups of pituitary autograft-bearing animals were treated with twice-daily injections of estradiol 17 beta (E), progesterone (P), estradiol 17 beta and progesterone (EP), or luteinizing hormone-releasing hormone (LRH). Within 2--4 hours following the last injection, the pituitary grafts were removed and placed into organ culture. They were maintained in culture with or without added LRH (10(-7) M) for 1 hour at 37 degrees C. The culture media were then frozen for later radioimmunoassay of FSH and LH. The tissues were kept in culture for an additional 24 hours, at which time they were fixed and prepared for immunocytochemistry or electron microscopy. Results showed that treatment of the animals with E, EP, or LRH enhanced the release of FSH and LH into the culture media, and that the release of these hormones was increased further by acute incubation with LRH. The ultrastructure of the gonadotrophs was well maintained by treating the animals with E or the combination of E and P or with LRH. Graft tissue from animals treated with LRH, which was incubated subsequently for 24 hours with LRH, showed the best maintenance of gonadotroph morphology. This experimental procedure should be useful for obtaining gonadotrophs for use in establishing gonadotroph cell lines.

摘要

将雌性斯普拉格-道利大鼠进行垂体切除,并立即将垂体前叶置于肾被膜下。术后1周,对携带垂体自体移植的动物组每日注射两次17β-雌二醇(E)、孕酮(P)、17β-雌二醇和孕酮(EP)或促黄体生成素释放激素(LRH)。在最后一次注射后的2 - 4小时内,取出垂体移植物并进行器官培养。将它们在添加或不添加LRH(10(-7) M)的情况下于37℃培养1小时。然后将培养基冷冻以备后续对促卵泡激素(FSH)和促黄体生成素(LH)进行放射免疫测定。将组织再培养24小时,此时将其固定并准备进行免疫细胞化学或电子显微镜检查。结果显示,用E、EP或LRH处理动物可增强FSH和LH向培养基中的释放,并且通过与LRH急性孵育可进一步增加这些激素的释放。通过用E或E与P的组合或LRH处理动物,促性腺激素细胞的超微结构得到了良好的维持。用LRH处理的动物的移植组织,随后与LRH一起孵育24小时,显示促性腺激素细胞形态维持得最好。该实验程序对于获取用于建立促性腺激素细胞系的促性腺激素细胞应该是有用的。

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