Kow L M, Harlan R E, Shivers B D, Pfaff D W
Brain Res. 1985 Aug 19;341(1):26-34. doi: 10.1016/0006-8993(85)91468-4.
In attempts to activate lordosis-facilitating neural mechanisms in the ventromedial hypothalamus (VMH), neural excitatory agents were infused into the medial hypothalamus, and the effects of the infusions on the lordosis reflex and on the electrical activity of VMH neurons were studied. Surprisingly, bilateral intrahypothalamic infusion of glutamate (10 mM, 1.0 microliter/side) into behaving, ovariectomized, estrogen-treated rats displaying moderate lordotic responsiveness did not facilitate lordosis, but instead, resulted in a rapid (within a few minutes) and transient (recovery in about 20 min) inhibition of lordosis. Further experiments showed that this lordosis-inhibiting effect of glutamate was dose-related, and was completely blocked by prior infusion of a local anesthetic, procaine. Infusion of KC1 (1.5 or 15%, 1.0 microliter/side) also induced a dose-related, rapid and transient inhibition of lordosis, that was essentially identical to that induced by glutamate. Kainic acid (0.25 micrograms/0.5 microliter/side) also caused a rapid inhibition of lordosis, but the effect was long-lasting (days). The inhibition of lordosis by these agents was dissociated in time course, presence, and/or severity from effects on non-lordotic behaviors. Electrophysiological studies showed that all three agents tested could excite multiunit activity of the VMH, and that the time courses of these excitations were closely comparable to those of the inhibition of lordosis induced by the respective agents. Altogether, these studies indicated that the excitation of certain medial hypothalamic neurons can inhibit the lordosis reflex. The implied lordosis-inhibiting neural mechanisms are separate from facilitatory mechanism(s), according to differences in latency, duration, and procaine-sensitivity of response.
为了激活腹内侧下丘脑(VMH)中促进脊柱前凸的神经机制,将神经兴奋性药物注入内侧下丘脑,并研究了注入药物对脊柱前凸反射和VMH神经元电活动的影响。令人惊讶的是,向表现出适度脊柱前凸反应的去卵巢、雌激素处理的大鼠双侧下丘脑内注入谷氨酸(10 mM,1.0微升/侧),并未促进脊柱前凸,反而导致脊柱前凸迅速(几分钟内)且短暂(约20分钟后恢复)受到抑制。进一步的实验表明,谷氨酸的这种抑制脊柱前凸的作用与剂量相关,并且在预先注入局部麻醉药普鲁卡因后完全被阻断。注入KCl(1.5%或15%,1.0微升/侧)也会引起与剂量相关的、快速且短暂的脊柱前凸抑制,这与谷氨酸诱导的抑制基本相同。 kainic酸(0.25微克/0.5微升/侧)也会导致脊柱前凸迅速受到抑制,但这种作用是持久的(数天)。这些药物对脊柱前凸的抑制在时间进程、存在情况和/或严重程度上与对非脊柱前凸行为的影响不同。电生理研究表明,所测试的这三种药物都能激发VMH的多单位活动,并且这些激发的时间进程与各自药物诱导的脊柱前凸抑制的时间进程密切可比。总之,这些研究表明,某些内侧下丘脑神经元的兴奋可以抑制脊柱前凸反射。根据反应的潜伏期、持续时间和对普鲁卡因的敏感性差异,暗示的抑制脊柱前凸的神经机制与促进机制是分开的。