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NMDA receptor antagonists dextromethorphan

It is beheved that phenomena such as sensitization, tolerance and drug-dependence might also involve synaptic plasticity. In fact, numerous studies indicate that NMDA receptor antagonists block sensitization to amphetamine and cocaine as well as tolerance and dependence to ethanol and opioids in animal models (Trujillo and Akil 1991 Pasternak and Inturrisi 1995 Trujillo and Akil 1995 Mao 1999). Recent studies indicate that the uncompetitive NMDA receptor antagonists dextromethorphan, memantine and neramexane not only prevent the development of morphine tolerance, but also reverse estabhshed tolerance in the continuing presence of this opioid, prevent the expression of withdrawal symptoms in rats (Popik and Skolnick 1996 Popik and Danysz 1997 Popik and Kozela 1999 Houghton et al. 2001) and attenuate the expres-... [Pg.279]

Hehny SA, Bah A. The effect of the preemptive use of the NMDA receptor antagonist dextromethorphan on postoperative analgesic requirements. Anesth Analg 2001 92(3) 739-44. [Pg.1091]

Memantine (Namenda) [Anti Alzheimer Agent/NMDA Receptor Antagonist] Uses Mod/ evere Alzheimer Dz Action N-methyl-D-aspartate recqjtor antagonist Dose Target 20 mg/d, start 5 mg/d, t 5 mg/d to 20 mg/d, wait >1 wk before t dose use doses if >5mg/d Caution [B, /-] Hqjatic/mild-mod renal impair Disp Tabs, sol SE Dizziness Interactions t Effects W amantadine, carbonic anhydrase inhibitors, dextromethorphan, ketamine, Na bicarbonate t effects W/ any drug, herb, food that alkalinizes urine EMS Use NaHCOs w/ caution OD May cause restlessness, hallucinations, drowsiness, and fainting symptomatic and supportive... [Pg.215]

Memantine is not a major substrate for hepatic cytochrome P450 isoenzymes and has not been shown to significantly inhibit or induce these enzymes. However, memantine is partially excreted by renal tubular secretion. Thus, concomitant use of other medications that use the same renal system (i.e., triampterene, hydrochlorothiazide, digoxin, cimetidine, ranitidine, metformin, and quinidine) may affect plasma levels of both drugs (Namenda 2005). Memantine should not be used in combination with other NMDA receptor antagonists, such as amantadine or dextromethorphan, because these combinations have not been formally studied. The clearance of memantine can be reduced when the urine is alkalinized, such as with the concomitant use of sodium bicarbonate or carbonic anhy-... [Pg.212]

Caruso FS, Goldblum R. Dextromethorphan, an NMDA receptor antagonist, enhances the analgesic properties of morphine. Inflammopharmacology 2000 8 161-73. [Pg.1092]

Popik, P., Kozela, E and Danysz, W. (2000). Clinically available NMDA receptor antagonists memantine and dextromethorphan reverse existing tolerance to the antinociceptive effects of morphine in mice. Naunyn-Sehmied. Arch Pharmacol. 361,... [Pg.45]

A few infants have been treated with antagonists of the NMDA receptor, an excitatory glutamatergic receptor for which glycine is a co-agonist (see Ch. 15) [29], Ketamine and dextromethorphan have been used with inconclusive results. Some infants may have had an improvement of their irritability and electroencephalogram. One infant, treated with both benzoate and dextromethorphan, was seizure-free by 12 months of age and had only moderately delayed development. However, this favorable experience has not always been duplicated. Treatment with dextromethorphan at the recommended dosage (maximum 5mg/kg/day) seems to be well-tolerated. [Pg.674]


See other pages where NMDA receptor antagonists dextromethorphan is mentioned: [Pg.931]    [Pg.261]    [Pg.280]    [Pg.254]    [Pg.709]    [Pg.931]    [Pg.1070]    [Pg.1102]    [Pg.234]    [Pg.127]    [Pg.313]    [Pg.322]    [Pg.322]    [Pg.463]    [Pg.286]    [Pg.413]    [Pg.97]    [Pg.1089]    [Pg.634]    [Pg.171]    [Pg.312]    [Pg.60]   
See also in sourсe #XX -- [ Pg.313 , Pg.324 ]




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NMDA

NMDA antagonists

NMDA receptor antagonists

NMDA receptors

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