Depaulis A, Keay K A, Bandler R
Neurobiologie et Neuropharmacologie des épilepsies généralisées, U.398 INSERM, Centre de Neurochimie, Strasbourg, France.
Exp Brain Res. 1994;99(1):75-83. doi: 10.1007/BF00241413.
Much evidence suggests that the midbrain periaqueductal gray region (PAG) plays a pivotal role in mediating an animal's responses to threatening, stressful, or painful stimuli. Active defensive reactions, hypertension, tachycardia and tachypnea are coordinated by a longitudinally oriented column of cells, found lateral to the midbrain aqueduct, in the caudal two-thirds of the PAG. In contrast, microinjections of excitatory amino acid (EAA) made in the ventrolateral region of the PAG in anesthetized or isolated animals evoke hypotension, bradycardia, and behavioral arrest. The aim of the present study was to examine further the effects of activation of neurons in the ventrolateral PAG. By injecting into this region low doses (40 pmol) of kainic acid (KA), a long-acting EAA, it was possible to observe a freely moving rat's behavior in a social situation (i.e., paired with a weight-matched, untreated partner). Such injected rats become quiescent, i.e., there was a cessation of all ongoing spontaneous activity. These rats were also hyporeactive: the investigative approaches of the partner failed to evoke orientation, startle reactions, or vocalization. Electroencephalographic measurements indicated that the effects of injections of KA in the ventrolateral PAG were not secondary to seizure activity. In addition to the quiescence and hyporeactivity reported here, and the hypotension and bradycardia reported previously, the ventrolateral PAG is a part of the brain from which analgesia has been readily evoked by electrical stimulation, or microinjections of either EAA or morphine. As a reaction to "deep" or "inescapable" pain, chronic injury, or defeat, animals often reduce their somatomotor activity, become more solitary, and are generally much less responsive to their environment.(ABSTRACT TRUNCATED AT 250 WORDS)
许多证据表明,中脑导水管周围灰质区域(PAG)在介导动物对威胁性、应激性或疼痛性刺激的反应中起关键作用。主动防御反应、高血压、心动过速和呼吸急促由位于中脑导水管外侧、PAG尾侧三分之二处的纵向排列的细胞柱协调。相比之下,在麻醉或分离的动物中,向PAG腹外侧区域微量注射兴奋性氨基酸(EAA)会引起低血压、心动过缓和行为停止。本研究的目的是进一步研究激活PAG腹外侧神经元的作用。通过向该区域注射低剂量(40皮摩尔)的海人酸(KA,一种长效EAA),可以观察自由活动大鼠在社交情境(即与体重匹配的未处理伙伴配对)中的行为。此类注射大鼠会变得安静,即所有正在进行的自发活动停止。这些大鼠还反应低下:伙伴的探究行为未能引发定向、惊吓反应或发声。脑电图测量表明,向PAG腹外侧注射KA的作用并非继发于癫痫活动。除了此处报告的安静和反应低下,以及先前报告的低血压和心动过缓外,PAG腹外侧还是通过电刺激或微量注射EAA或吗啡很容易诱发镇痛的脑区的一部分。作为对“深部”或“无法逃避”的疼痛、慢性损伤或挫败的反应,动物通常会减少其躯体运动活动,变得更加孤僻,并且对环境的反应通常会大大降低。(摘要截短于250字)