Login / Signup

Cytogenotoxicity effects in addicts with multidrug consumption.

Ana Elizabeth González-SantiagoAlejandro Salvador Gómez-CabreraRaúl Cuauhtémoc Baptista-RosasGuillermo Moisés Zúñiga-GonzálezBelinda Claudia Gómez-MedaAna Alondra Sobrevilla NavarroMaría Guadalupe Sánchez-Parada
Published in: Environmental and molecular mutagenesis (2024)
Drug abuse is considered a global health problem with serious social impact. In recent decades, changes in drug consumption patterns have shown a clear rising trend in the use of multiple drugs. Although the buccal micronucleus cytome (BMCyt) assay has evaluated cytotoxicity in drug abuse, there has not been an approach that takes into account this pattern of multiple drug use. Therefore, in this study, we evaluate for the first time the cytogenotoxic effects in multidrug users, and its correlation with the amount consumed and years of abuse. This study was conducted on 166 individuals by the BMCyt assay. A total of 83 individuals with a history of multiple licit (alcohol and tobacco) and at least one illicit drug abuse (marijuana, methamphetamines, cocaine, and/or inhalants), and 83 healthy individuals, non-drug abusers were analyzed. The results showed that drug abusers had higher frequencies of nuclear abnormalities nuclear buds, binucleated cells, pyknotic nuclei (PNs), karyorrhexis (KX), and abnormally condensed chromatin when compared with healthy controls. Moreover, results suggests that the use of licit and illicit drugs is related to cytogenotoxic damage, as was shown by an upward trend in the frequency of nuclear abnormalities identified in groups 1 (alcohol + tobacco + at least one illicit drug) and 2 (tobacco + at least one illicit drug). Furthermore, a positive correlation was found in the different groups, between the years and the amount of consumption of some drugs (alcohol, methamphetamine, and tobacco) with cytotoxicity markers such as KL, KX, and PNs.
Keyphrases
  • drug induced
  • adverse drug
  • public health
  • emergency department
  • gene expression
  • oxidative stress
  • high throughput
  • dna damage
  • drug resistant
  • transcription factor
  • induced apoptosis
  • multidrug resistant
  • signaling pathway