Lee W, Watanabe M, Glass J D
Department of Biological Sciences, Kent State University, OH 44240, USA.
Brain Res. 1995 Aug 28;690(1):64-72. doi: 10.1016/0006-8993(95)00588-h.
Immunohistochemical and immunoblot procedures were used to examine the effects of inhibitory short day (SD) photoperiod on the expression of neural cell adhesion molecule (NCAM) and its polysialylated form (PSA-NCAM) in the hypothalamus and preoptic area (POA) of the adult male Siberian hamster. In animals that had undergone SD-induced gonadal regression, immunoblot analyses revealed significant reductions in the content of immunoreactive PSA in anterior hypothalamic (AH) and mediobasal hypothalamic (MBH) regions. These changes were accompanied by increased contents of the 180 kDa NCAM isoform in the POA and AH, and decreased content in the MBH. The 140 kDa NCAM isoform also was elevated in the AH. Light microscopic analysis revealed a marked reduction in the density of NCAM-immunoreactive tanycyte-like processes in the MBH of animals exposed to SD. This effect was not blocked by castration, indicating that this may be a primay (sex steroid-independent) effect of altered photoperiod in the hypothalamus. Also, photoperiod-induced alterations in NCAM expression were not evident in non-responsive hamsters that maintained active testes under SD exposure. Collectively, these results are evidence that seasonal changes in photoperiod affect the expression of NCAM and PSA in the hypothalamus. Such changes could help promote plastic morphological rearrangements related to the regulation of seasonal reproductive and/or metabolic cycles.
采用免疫组织化学和免疫印迹法,研究抑制性短日照(SD)光周期对成年雄性西伯利亚仓鼠下丘脑和视前区(POA)神经细胞黏附分子(NCAM)及其多唾液酸化形式(PSA-NCAM)表达的影响。在经历了SD诱导性腺退化的动物中,免疫印迹分析显示下丘脑前部(AH)和下丘脑中间基底部(MBH)区域中免疫反应性PSA的含量显著降低。这些变化伴随着POA和AH中180 kDa NCAM异构体含量的增加,以及MBH中含量的降低。140 kDa NCAM异构体在AH中也有所升高。光学显微镜分析显示,暴露于SD的动物MBH中NCAM免疫反应性的类伸展细胞样突起的密度显著降低。去势并未阻止这种效应,这表明这可能是下丘脑光周期改变的一种主要(不依赖性类固醇)效应。此外,在SD暴露下保持睾丸活跃的无反应仓鼠中,光周期诱导的NCAM表达变化并不明显。总的来说,这些结果证明光周期的季节性变化会影响下丘脑NCAM和PSA的表达。这种变化可能有助于促进与季节性生殖和/或代谢周期调节相关的可塑性形态重排。