Kjaer A, Larsen P J, Knigge U, Warberg J
Department of Medical Physiology, Panum Institute, University of Copenhagen, Denmark.
Endocrinology. 1995 May;136(5):2189-97. doi: 10.1210/endo.136.5.7720668.
Dehydration associated with hyperosmolality and decreased extracellular volume stimulates arginine vasopressin (AVP) and oxytocin (OT) secretion from magnocellular neurons of the hypothalamus. The effects of hyperosmolality and decreased extracellular volume on the magnocellular neurons are mainly indirect and seem to be mediated centrally via several neurotransmitters and neuropeptides. Because histamine (HA), which serves as a central neurotransmitter, releases AVP and OT from the neurohypophysis when administered centrally, we investigated the possible role of HA in dehydration-induced AVP and OT secretion. To do this, we studied 1) the effect of dehydration on messenger RNA (mRNA) expression of the HA synthesis enzyme, histidine decarboxylase (HDC), in the tuberomammillary nucleus of the hypothalamus; and 2) the effect of HA synthesis inhibition during dehydration on AVP and OT mRNA expression in the supraoptic nucleus of the hypothalamus as well as on plasma AVP and OT levels. Forty-eight hours of dehydration increased the mRNA level of HDC in the tuberomammillary nuclei, whereas 24 h of dehydration had no effect. Pretreatment with the HA synthesis inhibitor alpha-fluoromethylhistidine (alpha FMH) increased the expression of HDC mRNA in 24-h dehydrated rats, but had no effect in euhydrated rats. In rats dehydrated for 48 h, the already increased level of HDC mRNA was not increased further by alpha FMH. Twenty-four and 48 h of dehydration increased AVP and OT mRNA levels in the supraoptic nucleus. This effect was inhibited by alpha FMH pretreatment. Dehydration increased the plasma levels of AVP and OT to an extent which depended on the duration of dehydration. Pretreatment with alpha FMH inhibited the hormone responses to 24 h of dehydration, but did not affect the responses to 48 h of dehydration. Twenty-four and 48 h of dehydration had no significant effect on the contents of AVP and OT in the neurohypophysis, whereas pretreatment with alpha FMH combined with 48 h of dehydration led to depletion of AVP stores in the neurohypophysis. Based on the present findings, we conclude that hypothalamic histaminergic neurons are involved in the regulation of dehydration-induced stimulation of magnocellular AVP and OT neurons.
与高渗和细胞外液量减少相关的脱水刺激下丘脑大细胞神经元分泌精氨酸加压素(AVP)和催产素(OT)。高渗和细胞外液量减少对大细胞神经元的影响主要是间接的,似乎是通过几种神经递质和神经肽在中枢介导的。由于作为中枢神经递质的组胺(HA)在中枢给药时会从神经垂体释放AVP和OT,我们研究了HA在脱水诱导的AVP和OT分泌中的可能作用。为此,我们研究了:1)脱水对下丘脑结节乳头核中HA合成酶组氨酸脱羧酶(HDC)信使核糖核酸(mRNA)表达的影响;2)脱水期间HA合成抑制对下丘脑视上核中AVP和OT mRNA表达以及血浆AVP和OT水平的影响。48小时的脱水增加了结节乳头核中HDC的mRNA水平,而24小时的脱水则没有影响。用HA合成抑制剂α-氟甲基组氨酸(αFMH)预处理可增加24小时脱水大鼠中HDC mRNA的表达,但对正常水合大鼠没有影响。在48小时脱水的大鼠中,αFMH并未使已经升高的HDC mRNA水平进一步升高。24小时和48小时的脱水增加了视上核中AVP和OT的mRNA水平。这种作用被αFMH预处理所抑制。脱水使血浆AVP和OT水平升高,升高程度取决于脱水持续时间。αFMH预处理抑制了激素对24小时脱水的反应,但不影响对48小时脱水的反应。24小时和48小时的脱水对神经垂体中AVP和OT的含量没有显著影响,而αFMH预处理与48小时脱水相结合导致神经垂体中AVP储备的耗尽。基于目前的研究结果,我们得出结论,下丘脑组胺能神经元参与脱水诱导的大细胞AVP和OT神经元刺激的调节。