Köves K, Gottschall P E, Görcs T, Scammell J G, Arimura A
U.S. Japan Biomedical Research Laboratories, Tulane University, Belle Chasse, Louisiana 70037.
Endocrinology. 1990 Mar;126(3):1756-63. doi: 10.1210/endo-126-3-1756.
The presence and synthesis of vasoactive intestinal polypeptide (VIP) has been demonstrated in the rat anterior pituitary. It was recently confirmed that immunoreactive VIP is present in the anterior pituitary, and in a thyroid-deficient state, VIP could be detected by light microscopic immunohistochemistry. It has also been suggested that VIP plays a stimulatory role in PRL secretion. To gain more detailed information on the localization of VIP and the conditions that alter the synthesis of VIP, we examined VIP immunoreactivity using immunohistochemistry in pituitaries of normal male and cycling female rats and in those states in which PRL secretion was enhanced (pregnancy, lactation, long term estrogen treatment, and pituitary implanted under kidney capsule of normal or estrogen-treated female rats). In situ, implanted and cultured pituitary cells were stained for VIP immunoreactivity using the peroxidase-antiperoxidase method. VIP immunoreactivity was observed in about 45% of the male rats, in all estrogen-treated female rats, in the implanted pituitaries under the kidney capsule (three of five from estrogen-treated and one of five from intact females, respectively), and in the pituitary cell cultures derived from estrogen-treated rats. Using a double labeling procedure we have also observed PRL immunoreactivity in a small population of the VIP-positive cells. These results suggest a positive regulatory role of estrogen in expression of the VIP gene. The physiological and pathophysiological significance of VIP in PRL secretion, however, remains to be clarified.
血管活性肠肽(VIP)已在大鼠垂体前叶中被证实存在并可合成。最近证实,垂体前叶中存在免疫反应性VIP,并且在甲状腺功能减退状态下,通过光学显微镜免疫组织化学可检测到VIP。也有人提出,VIP在催乳素(PRL)分泌中起刺激作用。为了获得关于VIP定位以及改变VIP合成的条件的更详细信息,我们使用免疫组织化学方法检测了正常雄性大鼠和处于发情周期的雌性大鼠垂体中的VIP免疫反应性,以及在PRL分泌增强的状态下(妊娠、哺乳、长期雌激素处理以及将垂体植入正常或雌激素处理的雌性大鼠肾包膜下)的VIP免疫反应性。使用过氧化物酶-抗过氧化物酶方法对原位、植入和培养的垂体细胞进行VIP免疫反应性染色。在约45%的雄性大鼠、所有雌激素处理的雌性大鼠、肾包膜下植入的垂体(分别来自雌激素处理的大鼠中的五只中有三只,来自未处理雌性大鼠中的五只中有一只)以及源自雌激素处理大鼠的垂体细胞培养物中观察到VIP免疫反应性。使用双重标记程序,我们还在一小部分VIP阳性细胞中观察到PRL免疫反应性。这些结果表明雌激素在VIP基因表达中起正向调节作用。然而,VIP在PRL分泌中的生理和病理生理意义仍有待阐明。