Niacinamide helps lessen Anxiety

Dr. Weeks’ Comment: For more than 3 decades I have helped people get off addictive pharmaceutical drugs like Valium (diazepam) and Clonazepam and the SSRI and SSNI anti-depressants which are biochemically best equated to dissociative anesthetic agents which disrupt sleep and create fugue-like zombie trances. One powerful ally in this fight to restore biochemical integrity in anxious or depressed people is vitamin B3 in the niacinamide form aka “nicotinamide” (niacin, the other vitamin B3 version, is best used for support cardiac health). Here is an exciting article on this vitamin.

These results suggest that while nicotinamide may exert some neuronal depressant and anxiolytic activity…”

Br J Pharmacol. 1985 Mar; 84(3): 689–696. doi: 10.1111/j.1476-5381.1985.tb16151.xPMCID: PMC1987159PMID: 2985162

Central effects of nicotinamide and inosine which are not mediated through benzodiazepine receptors.

J. M. BoldC. R. Gardner, and  R. J. Walker

Abstract

The actions of nicotinamide and inosine were investigated on rat cerebellar Purkinje cells using ionophoretic and extracellular recording techniques. Ionophoretic application of nicotinamide or inosine showed that they were potent inhibitors of Purkinje cell firing. This inhibition differed from that induced by benzodiazepines in that it was not reversed by the GABA antagonists bicuculline methiodide and picrotoxin. RO 15-1788, the specific benzodiazepine antagonist, did not reverse the effects of nicotinamide. Chlordiazepoxide has been shown to increase significantly social interaction between pairs of male rats and this increase can be reversed by RO 15-1788, 20 mg kg-1 i.p. Nicotinamide also caused a small increase in social interaction but this effect was not reversed by the benzodiazepine antagonist. Inosine did not increase social interaction. [3H]-flunitrazepam binding studies showed that nicotinamide and inosine have only low affinities for the benzodiazepine binding site. These results suggest that while nicotinamide may exert some neuronal depressant and anxiolytic activity, its site of action appears not to be associated with the benzodiazepine receptor site. Similarly, inosine exerts a neuronal depressant effect dissimilar from that of benzodiazepines.

Full text

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
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