Ka. Keay et al., CARDIOVASCULAR EFFECTS OF MICROINJECTIONS OF OPIOID AGONISTS INTO THEDEPRESSOR REGION OF THE VENTROLATERAL PERIAQUEDUCTAL GRAY REGION, Brain research, 762(1-2), 1997, pp. 61-71
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, hyporeac
tivity, hypotension and bradycardia. Microinjections of both excitator
y amino acids and opioids into the ventrolateral periaqueductal gray h
ave 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. Subseque
ntly we studied for the first time, the effects of microinjections of
mu-, delta-, and kappa-opioid agonists made into the ventrolateral per
iaqueductal grey depressor region. In contrast to the effects of excit
atory amino acid injections, microinjections of the mu-opioid agonist
([D-Ala(2),N-Me-Phe(4),Gly-ol(5)]enkephalin) evoked hypertension and t
achycardia at approximately 50% of sites. Similar to excitatory amino
acid injections, microinjections of both the delta-opioid agonist ([D-
Pen(2),D-Pen(5)]enkephalin), and the kappa-opioid agonist idinyl)-1-ox
aspiro[4,5]dec-8-yl]-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 ventr
olateral periaqueductal gray neurons, or at different ventrolateral pe
riaqueductal gray synaptic locations (pre- or post-synaptic). (C) 1997
Elsevier Science B.V.