Vandermaelen C P, Aghajanian G K
Brain Res. 1983 Dec 19;289(1-2):109-19. doi: 10.1016/0006-8993(83)90011-2.
Extracellular and intracellular recordings were made from dorsal raphe (DR) neurons in frontal rat brain slices maintained in vitro. A population of neurons was found which displayed electrophysiological and pharmacological characteristics of serotonin-containing DR neurons recorded in vivo. Recorded extracellularly, these neurons displayed biphasic or triphasic action potentials of 1.5-3.0 ms duration, and discharged with a slow and steady rhythm. Recorded intracellularly these neurons displayed action potentials of about 1.8 ms duration, which were followed by large (10-20 mV) after hyperpolarizations which normally lasted 200-800 ms. These presumed serotonergic DR neurons were inhibited by LSD and serotonin. They were excited by norepinephrine, or the alpha-agonist phenylephrine, and these activations could be reduced or blocked by alpha-adrenoreceptor antagonists including the selective alpha 1-antagonist, prazosin. The major difference between the in vitro recordings and previous in vivo recordings from anesthetized animals was a reduction in the number of spontaneously firing DR neurons. This was probably due, at least in part, to a disfacilitation of serotonergic DR neurons in the slice caused by the functional removal of a tonic noradrenergic input.
在体外维持的额叶大鼠脑片中,对背侧中缝核(DR)神经元进行细胞外和细胞内记录。发现一群神经元,它们表现出在体内记录的含5-羟色胺DR神经元的电生理和药理学特征。在细胞外记录时,这些神经元表现出持续时间为1.5 - 3.0毫秒的双相或三相动作电位,并以缓慢而稳定的节律放电。在细胞内记录时,这些神经元表现出持续时间约为1.8毫秒的动作电位,随后是通常持续200 - 800毫秒的大(10 - 20毫伏)超极化后电位。这些推测为5-羟色胺能的DR神经元被麦角酸二乙酰胺(LSD)和5-羟色胺抑制。它们被去甲肾上腺素或α-激动剂苯肾上腺素兴奋,并且这些激活可以被包括选择性α1-拮抗剂哌唑嗪在内的α-肾上腺素能受体拮抗剂减少或阻断。体外记录与先前对麻醉动物的体内记录之间的主要差异是自发放电的DR神经元数量减少。这可能至少部分是由于切片中5-羟色胺能DR神经元因紧张性去甲肾上腺素能输入的功能性去除而导致的易化作用减弱。