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Last Updated: 3 years ago

Possible Interaction: Mecamylamine and Niacin

supplement:

Niacin

Research Papers that Mention the Interaction

Abstract Mecamylamine is an antihypertensive that acts via nicotinic antagonism and has been suggested as an aid in smoking cessation.
Psychopharmacology  •  1996  |  View Paper
On the other hand, the choice accuracy deficit induced by nicotinic blockade with mecamylamine is potentiated by haloperidol.
Behavioral and neural biology  •  1990  |  View Paper
This protective effect was completely reversed when nicotinic and melatonin receptors were blocked respectively by mecamylamine and luzindole.
Journal of pineal research  •  2010  |  View Paper
The nicotinic current triggered a depolarization event with a peak at +49.3 mV and a ‘plateau’ phase that ended at −23.9 mV, which was blocked by 10 μmol/L mecamylamine.
Journal of neurochemistry  •  2007  |  View Paper
On the other hand, a 3-mM concentration of the nicotinic ACh antagonist mecamylamine decreased spike firing of these interneurons.
Zoological science  •  2008  |  View Paper
Chlorisondamine and mecamylamine are nicotinic antagonists that produce both ganglionic and central blockade.
Journal of Pharmacology and Experimental Therapeutics  •  2004  |  View Paper
The release was completely blocked by nicotinic antagonists hexamethonium (100 μmol/l) and mecamylamine (10 μmol/l), and decreased by tetrodotoxin (0.3 μmol/l) and ω-conotoxin (0.1 μmol/l) to 17% and 27%, resp.
Neurochemical Research  •  2004  |  View Paper
Systemic injections of nicotinic blocking drugs such as dihydro-β-erytroidin or mecamylamine decrease or suppress the occurrence of RR; therefore, cholinergic synapses are involved in the RR generating process.
Experimental Brain Research  •  2004  |  View Paper
The nicotinic responses of cultured neurons were found to be blocked by mecamylamine and curare but highly resistant to alpha-bungarotoxin.
Archives of insect biochemistry and physiology  •  2003  |  View Paper
Mecamylamine , a broad‐spectrum nicotinic antagonist, reversibly inhibited nicotinic action.
The Journal of physiology  •  2001  |  View Paper
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