Keay K A, Crowfoot L J, Floyd N S, Henderson L A, Christie M J, Bandler R
Department of Anatomy and Histology and Institute for Biomedical Research, The University of Sydney, NSW, Australia.
Brain Res. 1997 Jul 11;762(1-2):61-71. doi: 10.1016/s0006-8993(97)00285-0.
Microinjections of excitatory amino acids made into the ventrolateral midbrain periaqueductal gray of the rat have revealed that neurons in this region integrate a reaction characterised by quiescence, hyporeactivity, hypotension and bradycardia. Microinjections of both excitatory amino acids and opioids into the ventrolateral periaqueductal gray have shown also that it is a key central site mediating analgesia. The effects of injections of opioids into the ventrolateral periaqueductal gray on arterial pressure and heart rate or behaviour are unknown. In this study we first mapped in the rat the extent of the ventrolateral periaqueductal gray hypotensive region as revealed by microinjections of excitatory amino acids. We found that ventrolateral periaqueductal gray depressor region extended more rostrally than previously thought into the tegmentum ventrolateral to the periaqueductal gray. Subsequently we studied for the first time, the effects of microinjections of mu-, delta-, and kappa-opioid agonists made into the ventrolateral periaqueductal grey depressor region. In contrast to the effects of excitatory amino acid injections, microinjections of the mu-opioid agonist ([D-Ala2,N-Me-Phe4,Gly-ol5]enkephalin) evoked hypertension and tachycardia at approximately 50% of sites. Similar to excitatory amino acid injections, microinjections of both the delta-opioid agonist ([D-Pen2,D-Pen5]enkephalin), and the kappa-opioid agonist ((5,7,8)-(+)-N-Methyl-N-[7-(1-pyrrolidinyl)-1-oxaspiro[4.5]dec-8-y l]-benzeneacetamide) evoked either a hypotension and bradycardia, or had no effect. These results indicate that different opiate receptor subtypes are present on a distinct population of ventrolateral periaqueductal gray neurons, or at different ventrolateral periaqueductal gray synaptic locations (pre- or post-synaptic).
向大鼠腹外侧中脑导水管周围灰质进行兴奋性氨基酸的微量注射后发现,该区域的神经元整合了一种以静止、反应性降低、低血压和心动过缓为特征的反应。向腹外侧导水管周围灰质同时注射兴奋性氨基酸和阿片类药物也表明,它是介导镇痛的关键中枢位点。向腹外侧导水管周围灰质注射阿片类药物对动脉血压、心率或行为的影响尚不清楚。在本研究中,我们首先通过兴奋性氨基酸微量注射,在大鼠中描绘出腹外侧导水管周围灰质降压区域的范围。我们发现,腹外侧导水管周围灰质降压区域比之前认为的更向头端延伸至导水管周围灰质腹外侧的被盖区。随后,我们首次研究了向腹外侧导水管周围灰质降压区域微量注射μ-、δ-和κ-阿片受体激动剂的效果。与兴奋性氨基酸注射的效果相反,μ-阿片受体激动剂([D-丙氨酸2,N-甲基苯丙氨酸4,甘醇5]脑啡肽)在大约50%的位点引起高血压和心动过速。与兴奋性氨基酸注射类似,δ-阿片受体激动剂([D-青霉胺2,D-青霉胺5]脑啡肽)和κ-阿片受体激动剂((5,7,8)-(+)-N-甲基-N-[7-(1-吡咯烷基)-1-氧杂螺[4.5]癸-八-基]-苯乙酰胺)的微量注射要么引起低血压和心动过缓,要么没有效果。这些结果表明,不同的阿片受体亚型存在于腹外侧导水管周围灰质神经元的不同群体上,或者存在于腹外侧导水管周围灰质不同的突触位置(突触前或突触后)。