首页> 外文期刊>Peptides: An International Journal >Developmental changes of hypothalamic, pituitary and striatal tachykinins in response to testosterone: influence of prenatal melatonin.
【24h】

Developmental changes of hypothalamic, pituitary and striatal tachykinins in response to testosterone: influence of prenatal melatonin.

机译:下丘脑,垂体和纹状体速激肽响应睾丸激素的发育变化:产前褪黑激素的影响。

获取原文
获取原文并翻译 | 示例
       

摘要

Substance P (SP) and neurokinin A (NKA), members of the family of mammalian tachykinins, are involved in the regulation of many physiological functions and are widely distributed in mammalian tissues. In this report, the effects of prenatal melatonin on the postnatal developmental pattern of NKA, and SP, and on testosterone secretion were investigated. Also, tachykinin response to the administration of testosterone propionate (TP) was studied. The brain areas studied were medio-basal-hypothalamus, pituitary gland and striatum. Male rat offspring of control or melatonin treated mother rats were studied at different ages of the sexual development: infantile, juvenile or prepubertal periods, and pubertal period. Both groups received exogenous TP (control-offspring+TP and MEL-offspring+TP), or the vehicle (control-offspring+placebo and MEL-offspring+placebo). Hypothalamic concentrations of all peptides studied in control-offspring+placebo remained at low levels until the juvenile period, days 30-31 of age. After this age, increasing concentrations of these peptides were found, with peak values at puberty, 40-41 days of age, then declining until adulthood. In the MEL-offspring+placebo a different pattern of development was observed; hypothalamic concentrations of NKA and SP from the infantile period until the end of juvenile period were significantly higher than in control-offspring+placebo. TP administration exerted a more marked influence on MEL-offspring than on control-offspring and prevented the elevation in tachykinin concentrations associated with prenatal melatonin treatment. TP administration to control-offspring resulted in significantly reduced (P < 0.05) tachykinin concentration only at 40-41 days of age, and increased (P < 0.01) during infantile period as compared to control-offspring+placebo. Pituitary NKA concentrations were lower than in the hypothalamus. In control-offspring+placebo pituitary NKA levels did not show significant changes throughout sexual development. A different developmental pattern was observed in MEL-offspring+placebo, with significantly increased (P < 0.05) pituitary NKA concentrations at 35-36 days of age than in control-offspring+placebo. TP administration to control-offspring influenced pituitary NKA levels at the end of the infantile and pubertal periods, showing at both stages significantly higher (P < 0.05) NKA levels as compared to control-offspring+placebo. NKA levels in MEL-offspring+TP were only affected at 21-22 days of age, showing significantly increased (P < 0.01) values as compared to MEL-offspring+placebo. Striatal tachykinin concentrations in control-offspring did not undergo important modifications throughout sexual development, but during the prepubertal period they started to increase. Maternal melatonin and TP injections produced short-lived alterations during the infantile period. The results showed that prenatal melatonin delayed the postnatal testosterone secretion pattern until the end of the pubertal period and postnatal peptide secretion in brain structures. Consequently, all functions depending of the affected areas will in turn, be affected.
机译:P(SP)和神经激肽A(NKA)是哺乳动物速激肽家族的成员,参与许多生理功能的调节,并广泛分布于哺乳动物组织中。在本报告中,研究了产前褪黑激素对NKA和SP产后发育方式以及睾丸激素分泌的影响。另外,还研究了速激肽对丙酸睾丸激素(TP)的反应。研究的大脑区域为中下丘脑,垂体和纹状体。研究了对照或褪黑素治疗的母鼠的雄性大鼠后代在不同年龄的性发育时期:婴儿期,少年期或青春期前和青春期。两组均接受外源TP(对照后代+ TP和MEL-后代+ TP)或媒介物(对照后代+安慰剂和MEL-后代+安慰剂)。在对照后代+安慰剂中研究的所有肽的下丘脑浓度一直保持低水平,直到30-31岁的少年时期。在这个年龄之后,发现这些肽的浓度增加,在青春期40-41天时达到峰值,然后下降直至成年。在MEL-后代+安慰剂中,观察到了不同的发育模式。从婴儿期到青少年期结束时,下丘脑的NKA和SP浓度显着高于对照后代+安慰剂。 TP给药对MEL后代的影响比对对照后代的影响更显着,并防止与产前褪黑激素治疗相关的速激肽浓度升高。与对照后代+安慰剂相比,TP对对照后代的施用仅在40-41天时显着降低(P <0.05)速激肽浓度,而在婴儿期增加(P <0.01)。垂体NKA浓度低于下丘脑。在对照后代+安慰剂中,垂体NKA水平在整个性发育过程中均未显示明显变化。在MEL-后代+安慰剂中观察到了不同的发育模式,与对照-后代+安慰剂相比,在35-36日龄时垂体NKA浓度显着增加(P <0.05)。在婴儿期和青春期结束时,给予对照后代的TP影响垂体NKA水平,与对照后代+安慰剂相比,这两个阶段的NKA水平均显着更高(P <0.05)。 MEL-后代+ TP中的NKA水平仅在21-22天龄时受到影响,与MEL-后代+安慰剂相比,其NKA值显着增加(P <0.01)。对照子代中纹状体速激肽的浓度在整个性发育过程中并未发生重要的改变,但在青春期前开始增加。母体褪黑激素和TP注射在婴儿期产生短暂的改变。结果表明,产前褪黑素会延迟产后睾丸激素的分泌方式,直至青春期末和脑结构中产后肽的分泌。因此,取决于受影响区域的所有功能将依次受到影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号