Therapeutic Properties of Ayahuasca Components in Ischemia/Reperfusion Injury of the Eye
Biomedicines – April 26, 2022
Source: OpenAlex
Summary
Harmaline, a compound in Ayahuasca, shows promise for protecting vision in ischemic eye diseases. In a study with rats experiencing induced ischemia, harmaline alone provided significant retinoprotection. However, when combined with N,N-dimethyltryptamine (DMT), this effect was negated. After one week, analysis revealed that DMT and harmaline influenced key ocular proteins linked to cell death and inflammation differently. With 60 rats involved, the findings suggest that while harmaline may be beneficial, the interaction with DMT warrants careful consideration in future therapeutic applications.
Abstract
Ischemic eye diseases are major causes of vision impairment. Thus, potential retinoprotective effects of N’N-dimethyltryptamine (DMT) were investigated. To inhibit its rapid breakdown by monoamine-oxidase A (MAO-A) enzyme, DMT was co-administered with harmaline, a β-carboline in the Amazonian Ayahuasca brew. Using ligation, 60 min of ischemia was provoked in eyes of rats, followed by 7 days of reperfusion whilst animals received harmaline alone, DMT + harmaline, or vehicle treatment. After 1 week of reperfusion, electroretinographical (ERG) measurements, histological analysis, and Western blot were performed. Harmaline alone exhibited retinoprotection in ischemia–reperfusion (I/R) which was, surprisingly, counterbalanced by DMT in case of co-administration. As both MAO-A inhibition and DMT increase serotoninergic tone synergistically, communicated to be anti-ischemic, thus, involvement of other pathways was investigated. Based on our experiments, DMT and harmaline exert opposite effects on important ocular proteins such as PARP1, NFκB, MMP9, or HSP70, each having a critical role in a different mechanism of eye-ischemia-related pathologies, e.g., cell death, inflammation, tissue destruction, and oxidative stress. Since DMT is proclaimed to be a promising drug candidate, its potentially undesirable effect on eye-ischemia should be further investigated. Meanwhile, this experiment revealed the potential therapeutic effect of MAO-A inhibitor harmaline in I/R-related eye diseases.