Opioid receptors
M Waldhoer, SE Bartlett… - Annual review of …, 2004 - annualreviews.org
▪ Abstract Opioid receptors belong to the large superfamily of seven transmembrane-
spanning (7TM) G protein-coupled receptors (GPCRs). As a class, GPCRs are of …
spanning (7TM) G protein-coupled receptors (GPCRs). As a class, GPCRs are of …
α2‐Adrenergic Receptor Subtypes — Novel Functions Uncovered in Gene‐Targeted Mouse Models
M Brede, M Philipp, A Knaus, V Muthig… - Biology of the …, 2004 - Wiley Online Library
Summry—The family of adrenergic receptors contains nine different subtypes of G protein‐
coupled receptors which mediate the biological effects of adrenaline and noradrenaline …
coupled receptors which mediate the biological effects of adrenaline and noradrenaline …
Actions of noradrenaline on substantia gelatinosa neurones in the rat spinal cord revealed by in vivo patch recording
M Sonohata, H Furue, T Katafuchi… - The Journal of …, 2004 - Wiley Online Library
To elucidate the mechanisms of antinociception mediated by the descending noradrenergic
pathway in the spinal cord, the effects of noradrenaline (NA) on noxious synaptic responses …
pathway in the spinal cord, the effects of noradrenaline (NA) on noxious synaptic responses …
Astrocytic adrenoceptors: a major drug target in neurological and psychiatric disorders?
L Hertz, Y Chen, ME Gibbs, P Zang… - Current Drug Targets …, 2004 - ingentaconnect.com
Considerable attention has recently been paid to astrocyte functions, which are briefly
summarized. A large amount of data is available about adrenoceptor expression and …
summarized. A large amount of data is available about adrenoceptor expression and …
[HTML][HTML] Stability of admixture containing morphine sulfate, bupivacaine hydrochloride, and clonidine hydrochloride in an implantable infusion system
AM Classen, GH Wimbish, TC Kupiec - Journal of pain and symptom …, 2004 - Elsevier
Intrathecal infusion is often performed using drug combinations. This study was conducted to
evaluate the stability of the admixture of morphine sulfate, bupivacaine hydrochloride, and …
evaluate the stability of the admixture of morphine sulfate, bupivacaine hydrochloride, and …
α2AAdrenoceptors Contribute to Feedback Inhibition of Capsaicin-induced Hyperalgesia
H Mansikka, J Lähdesmäki, M Scheinin… - The Journal of the …, 2004 - pubs.asahq.org
Background Studies on receptor knockout mice have so far shown that of the three alpha2-
adrenoceptor subtypes, the alpha (2A) adrenoceptor has a major role in mediating the …
adrenoceptor subtypes, the alpha (2A) adrenoceptor has a major role in mediating the …
INTERACTIONS BETWEEN δ OPIOID RECEPTORS AND α2A‐ADRENOCEPTORS
C Rios, I Gomes, LA Devi - Clinical and Experimental …, 2004 - Wiley Online Library
Several studies have reported functional interactions between different subtypes of opioid
and α2A‐adrenoceptors in the induction of spinal cord analgesia. The mechanisms …
and α2A‐adrenoceptors in the induction of spinal cord analgesia. The mechanisms …
α2-Adrenoreceptors Profile Modulation. 2. Biphenyline Analogues as Tools for Selective Activation of the α2C-Subtype
F Gentili, F Ghelfi, M Giannella… - Journal of medicinal …, 2004 - ACS Publications
A series of derivatives structurally related to biphenyline (3) was designed with the aim to
modulate selectivity toward the α2-AR subtypes. The results obtained demonstrated that the …
modulate selectivity toward the α2-AR subtypes. The results obtained demonstrated that the …
Antinociceptive properties of fadolmidine (MPV‐2426), a novel α2‐adrenoceptor agonist
A Pertovaara - CNS drug reviews, 2004 - Wiley Online Library
ABSTRACT Fadolmidine (MPV‐2426) is a novel α2‐adrenoceptor (α2‐AR) agonist
developed for spinal analgesia. It is highly selective for α2‐ARs, but it lacks subtype …
developed for spinal analgesia. It is highly selective for α2‐ARs, but it lacks subtype …
Dextromethorphan potentiates morphine-induced antinociception at both spinal and supraspinal sites but is not related to the descending serotoninergic or adrenergic …
LH Chow, EYK Huang, ST Ho, SK Tsai… - Journal of biomedical …, 2004 - Springer
Morphine is a strong and widely used opioid analgesic in pain management, but some
adverse effects limit its clinical use at high doses. The clinically available non-opioid …
adverse effects limit its clinical use at high doses. The clinically available non-opioid …