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雌激素与雌性大鼠发育中性二态性视前区的细胞凋亡

Estrogen and apoptosis in the developing sexually dimorphic preoptic area in female rats.

作者信息

Arai Y, Sekine Y, Murakami S

机构信息

Department of Anatomy, Juntendo University School of Medicine, Tokyo, Japan.

出版信息

Neurosci Res. 1996 Aug;25(4):403-7. doi: 10.1016/0168-0102(96)01070-x.

Abstract

Effect of estrogen on apoptotic cell death was studied in the two sexually dimorphic neuronal groups in the developing rat preoptic area (POA): the anteroventral periventricular nucleus of the POA (AVPvN-POA); and the sexually dimorphic nucleus of the POA (SDN-POA). A specific labelling of nuclear fragmentation was performed by terminal deoxynucleotydyl transferase(TdT)-mediated dUTP-biotin nick end-labeling method (TUNEL method) to demonstrate apoptosis. In the AVPvN-POA whose size is larger in females than in males, the number of TUNEL-positive cells was not significantly different between day 5 control and female pups sacrificed 10 h after 25 micrograms estradiol benzoate (EB) injection. However, TUNEL-positive cells showed a significant increase in the female pups sacrificed 24 h after EB injection, compared to that shown in the control female pups. In the SDN-POA whose size is larger in males than in females, EB injection significantly decreased TUNEL-positive cells in the female pups sacrificed 24 h after EB injection, compared to that in controls. These results suggest that estrogen regulates the neuronal number by facilitating apoptotic cell death in the developing AVPvN-POA or by inhibiting it in the developing SDN-POA.

摘要

在发育中的大鼠视前区(POA)的两个性别二态性神经元群中研究了雌激素对凋亡细胞死亡的影响:视前区腹侧前室周核(AVPvN-POA);以及视前区性别二态核(SDN-POA)。通过末端脱氧核苷酸转移酶(TdT)介导的dUTP-生物素缺口末端标记法(TUNEL法)对核碎裂进行特异性标记,以证明细胞凋亡。在雌性比雄性体积更大的AVPvN-POA中,在第5天对照与注射25微克苯甲酸雌二醇(EB)10小时后处死的雌性幼崽之间,TUNEL阳性细胞的数量没有显著差异。然而,与对照雌性幼崽相比,在EB注射24小时后处死的雌性幼崽中,TUNEL阳性细胞显著增加。在雄性比雌性体积更大的SDN-POA中,与对照组相比,EB注射显著减少了在EB注射24小时后处死的雌性幼崽中的TUNEL阳性细胞。这些结果表明,雌激素通过促进发育中的AVPvN-POA中的凋亡细胞死亡或抑制发育中的SDN-POA中的凋亡细胞死亡来调节神经元数量。

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