Abstract

Harmane, a potent neurotoxin linked with several neurological disorders, is present in many foods, coffee, and cigarettes. We assessed whether morning food/coffee consumption and smoking were reflected in blood harmane concentrations (BHCs) we obtained in an epidemiologic sample (n = 497). Participants who smoked on the morning of phlebotomy had similar logBHCs to those who had not smoked (P = .57); there was no correlation between logBHCs and number of cigarettes (P = .59). Among the coffee drinkers, there was no correlation between number of cups and logBHCs (P = .98). Participants who had eaten on the morning of phlebotomy had similar logBHCs to those who had not (P = .49); logBHCs did not correlate with the time latency between last food consumption and phlebotomy (P = .74). BHCs in this sample of ~500 individuals did not covary with recent smoking, coffee, or food consumption, suggesting that our inability to withhold these exposures on the morning of phlebotomy was not reflected in the BHCs we measured.

Highlights

  • Harmane (1-methyl-9H-pyrido[3,4-β]indole) is a potent neurotoxin that has been linked with several neurological outcomes [1, 2]

  • We assessed whether morning food/coffee consumption and smoking were reflected in blood harmane concentrations (BHCs) we obtained in an epidemiologic sample (n = 497)

  • Participants who had eaten on the morning of phlebotomy had similar logBHCs to those who had not (P = .49); logBHCs did not correlate with the time latency between last food consumption and phlebotomy (P = .74)

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Summary

Introduction

Harmane (1-methyl-9H-pyrido[3,4-β]indole) is a potent neurotoxin that has been linked with several neurological outcomes [1, 2]. It is produced endogenously by the body, harmane is present in many foods Smoking [8] and food ingestion [9] have been shown to result in transient elevations in BHCs. After smoking, blood harmane levels rise rapidly and seem to return to baseline within one hour, the number of tested human volunteers has been small (n = 3) [8]. After oral dosing (harmane dissolved in corn oil), blood harmane levels in rats peaked rapidly (in approximately 30 minutes) and gradually returned to baseline within 3–5 hours [9]

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