Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Y O, Taiwo"'
Publikováno v:
Annals of the Rheumatic Diseases. 58:357-365
OBJECTIVES Chondrocytic matrix metalloproteinases (MMPs) are believed to be important in osteoarthritic cartilage degradation. The cartilage lesion of osteoarthritis (OA) is focal and often progressive. During its development chondrocytes differentia
Publikováno v:
Brain Research. 608:87-94
This study evaluated the antinociceptive effects produced when different combinations of supraspinal mu- and delta-opioid agonists were co-administered with spinal mu-, delta-, and kappa-opioid agonists. Using the Randall-Selitto paw-withdrawal test,
Publikováno v:
Journal of Neurophysiology. 66:729-734
1. In this study we used psychophysical experiments in humans and behavioral and electrophysiological studies in rats to evaluate nociceptive and C-fiber mechanoheat nociceptor (C-MH) responses to sustained mechanical stimuli that are initially nonpa
Publikováno v:
University of Manchester-PURE
Scopus-Elsevier
Scopus-Elsevier
OBJECTIVES—Matrix metalloproteinases (MMPs) are thought to be major mediators of cartilage destruction. Osteoarthritis (OA) is characterised by cartilage degradation. This study explores gene expression of three MMPs in articular chondrocytes durin
Publikováno v:
Brain research. 509(1)
This study evaluated the interaction of the analgesic effects of a selective kappa- (U50, 488H) and a selective delta- ([D-Pen2,5]enkephalin, DPDPE) opioid agonist, co-injected intrathecally, using the Randall-Selitto paw-withdrawal test, in the rat.
Publikováno v:
Journal of Clinical Investigation. 82:1574-1577
The analgesia produced by combinations of low-dose naloxone with pentazocine or morphine was studied in 105 patients with moderately severe postoperative pain after standardized surgery for removal of impacted third molars. Pain intensity was quantif
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 249(1)
This study addressed the opiate receptor subclass which underlies the paradoxical analgesic action of intrathecal administration of low doses of the stereospecific opiate receptor antagonist, naloxone. The analgesic effect of low dose naloxone was ab