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Reprod Sci ; 31(5): 1278-1289, 2024 May.
Article in English | MEDLINE | ID: mdl-38228974

ABSTRACT

Concerns have been raised about potentially irreversible brain damage and damage to the neuroendocrine system during development when treating attention-deficit/hyperactivity disorder with lisdexamfetamine (LDX), a norepinephrine dopamine reuptake inhibitor. This study aims to elucidate the potential adverse effects of LDX on the male reproductive system due to its widespread use and potential for abuse. In this study, adult male rats were randomized into control and LDX groups. Thirty milligrams per kilogram LDX was administered orally for 3 weeks. After isolation of epididymal spermatozoa, the rats were euthanized and testicular tissues were collected for stereological and molecular analyses. The LDX group showed a decrease in sperm motility and an increase in DNA fragmentation compared to the control group. There was also a dramatic decrease in testosterone in the LDX group. Testicular expression of caspase-3 and TNF-α was significantly increased in the LDX group. According to our findings, prolonged use of LDX leads to reduced sperm quality. It also induces apoptosis, inflammatory response, and pathological changes in the testicular tissue. What we have observed in this study is noteworthy but requires further investigation, particularly in people who use LDX over a longer period of time.


Subject(s)
Apoptosis , Lisdexamfetamine Dimesylate , Sperm Motility , Spermatozoa , Testis , Animals , Male , Apoptosis/drug effects , Spermatozoa/drug effects , Spermatozoa/pathology , Lisdexamfetamine Dimesylate/toxicity , Testis/drug effects , Testis/pathology , Testis/metabolism , Sperm Motility/drug effects , Rats, Sprague-Dawley , Inflammation/chemically induced , Inflammation/pathology , Rats , Testosterone , DNA Fragmentation/drug effects , Caspase 3/metabolism
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