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Chunk #23 — Discussion

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Association between single nucleotide polymorphisms in the mu opioid receptor gene (OPRM1) and self-reported responses to alcohol in American Indians.
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The CNS effects of alcohol range from mild euphoria (high), to impaired coordination, to ataxia, decreased mentation, labile mood, to poor judgment, slurred speech, nausea and vomiting, and finally to respiratory failure, coma and death, depending on the dose imbibed [89]. The final level of impairment appears to depend on a number of factors including a persons' gender, age, weight, prior experience with alcohol and level of tolerance [40]. Another source of variation in response to alcohol is individual variation in alcohol metabolism. Some individuals, particularly East Asians who are homozygous for the ALDH2*2 allele, are intolerant of alcohol and report intense facial flushing, tachycardia, hypotension, headache, nausea and vomiting following drinking more than one drink [67]. African Americans, with at least one ADH1B*3, also report expecting to have a more intense response to a standard dose of alcohol when compared to African Americans who are homozygous for the ADH1B*1 allele [90].