共 7 条
[1]
The NMDA receptor antagonists, LY 2764614 and MK 801, and the nitric oxide synthase inhibitor NG-Nitro-L-arginine, attenuate analgesic tolerance to the mu-opioid morphine but not to kappa opioids. Elliott K,Minamlni N,Koiesnikov Y et al. Pain . 1993
[2]
Inhibition of nitric oxide synthase enhances antinociception mediated by mu,delta and kappa opioid receptors in acute and prolonged pain in the rat spinal cord. Halina M,Dominika L,Ryszard P et al. Journal of Pharmacology and Experimental Therapeutics . 1997
[3]
Formalin-evoked fos expressing is enhanced in morphine-tolerant rats. Rohde DS,Detweiler DJ,Bashaum AI et al. Brain Research . 1997
[4]
Repetitive opioid abstinence causes progressive hyperalgesia sensitive to N-methl-D-aspartate receptor in the rat. Dunber SA,Pulai LJ. Journal of Pharmacology and Experimental Therapeutics . 1998
[5]
NG-Nitro-Larginine methyl ester exhibits antinociceptive activity in the mouse. Moore PK,Oluyomi AO,Babbedge RC et al. British Journal of Pharmacology . 1991
[6]
Molecular biology of pain. Munglani R,Hunt SP. British Journal of Anaesthesia . 1995
[7]
Nitric oxide and opioid tolerance. Babey AM,Kolesnikov Y,Cheng J et al. Neuropharmacology . 1994