Comparative Effects of L-Carnitine and T-Bhq on Reproductive Hormone Dysregulation in Alcohol-Exposed Wistar Rats

Background: Reproductive dysfunction has been linked to chronic alcoholism, especially due to oxidative stress. Antioxidants like L-carnitine and tert-butylhydroquinone (tBHQ) could mitigate alcohol-induced reproductive toxicity, but their comparative effects are understudied. This study compared the effects of l-carnitine and t-BHQ on reproductive hormone dysregulation in alcohol-exposed Wistar rats. Methodology: Thirty-five male Wistar rats were divided into seven groups (n=5): control, alcohol-only, alcohol+L-carnitine, alcohol+tBHQ, alcohol+L-carnitine+tBHQ, L-carnitine-only, and tBHQ-only. Alcohol was administered orally (2 g/kg/day), L-carnitine (100 mg/kg/day), and tBHQ (50 mg/kg/day) for 60 days. At the end of the experimental period, serum testosterone, dihydrotestosterone (DHT), 5-α reductase, luteinizing hormone (LH), and follicle stimulating hormone (FSH) were assayed. Results: Alcohol exposure significantly reduced testosterone (from 10.33 ng/ mL in the control group to 1.12 ng/mL) while significantly increasing the levels of DHT (59.67 pg/Ml to 1237.67 pg/mL), 5-α reductase (91.83 pg/mL to 698.33 pg/mL), LH (26.83 mIU/mL to 64.50 mIU/mL) and FSH (2.98 mIU/mL to 18.33 mIU/mL). L-carnitine and tBHQ independently restored testosterone to above-control levels (16.67 and 17.33 ng/mL, respectively), with their co-administration yielded much more increase. Both agents significantly reduced alcohol-induced increase in DHT and 5-α reductase, with tBHQ exerting a stronger suppressive effect. Similarly, LH and FSH concentrations were normalized toward control values following treatment. Conclusion: Results shows that L-carnitine and tBHQ mitigated hormone dysregulation in male Wistar rats caused by excessive alcohol exposure. These findings suggest that L-carnitine preserves mitochondrial integrity to sustain steroidogenesis, while tBHQ more effectively modulates enzyme activity and oxidative stress in the testes.

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Journal
TNHJPH
Published
2025-10-26
DOI
https://doi.org/10.71637/tnhj.v25i4.1248
Primary Topic
Prenatal Substance Exposure Effects
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article
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article

Comparative Effects of L-Carnitine and T-Bhq on Reproductive Hormone Dysregulation in Alcohol-Exposed Wistar Rats

Jessica Tochukwu Nzeadibe, Exploit Ezinne Chukwuka, John Atambell Okwejie John Atambell Okwejie, Polycarp Unim Adie et al.
TNHJPH
Prenatal Substance Exposure Effects
article

Comparative Effects of L-Carnitine and T-Bhq on Reproductive Hormone Dysregulation in Alcohol-Exposed Wistar Rats

Jessica Tochukwu Nzeadibe, Exploit Ezinne Chukwuka, John Atambell Okwejie John Atambell Okwejie, Polycarp Unim Adie, Atim Okpo-Ene, Victor Essien, Minafuro Okwejie, Okoi Okoi, Nyakno Godwin
article en

Abstract

Background: Reproductive dysfunction has been linked to chronic alcoholism, especially due to oxidative stress. Antioxidants like L-carnitine and tert-butylhydroquinone (tBHQ) could mitigate alcohol-induced reproductive toxicity, but their comparative effects are understudied. This study compared the effects of l-carnitine and t-BHQ on reproductive hormone dysregulation in alcohol-exposed Wistar rats. Methodology: Thirty-five male Wistar rats were divided into seven groups (n=5): control, alcohol-only, alcohol+L-carnitine, alcohol+tBHQ, alcohol+L-carnitine+tBHQ, L-carnitine-only, and tBHQ-only. Alcohol was administered orally (2 g/kg/day), L-carnitine (100 mg/kg/day), and tBHQ (50 mg/kg/day) for 60 days. At the end of the experimental period, serum testosterone, dihydrotestosterone (DHT), 5-α reductase, luteinizing hormone (LH), and follicle stimulating hormone (FSH) were assayed. Results: Alcohol exposure significantly reduced testosterone (from 10.33 ng/ mL in the control group to 1.12 ng/mL) while significantly increasing the levels of DHT (59.67 pg/Ml to 1237.67 pg/mL), 5-α reductase (91.83 pg/mL to 698.33 pg/mL), LH (26.83 mIU/mL to 64.50 mIU/mL) and FSH (2.98 mIU/mL to 18.33 mIU/mL). L-carnitine and tBHQ independently restored testosterone to above-control levels (16.67 and 17.33 ng/mL, respectively), with their co-administration yielded much more increase. Both agents significantly reduced alcohol-induced increase in DHT and 5-α reductase, with tBHQ exerting a stronger suppressive effect. Similarly, LH and FSH concentrations were normalized toward control values following treatment. Conclusion: Results shows that L-carnitine and tBHQ mitigated hormone dysregulation in male Wistar rats caused by excessive alcohol exposure. These findings suggest that L-carnitine preserves mitochondrial integrity to sustain steroidogenesis, while tBHQ more effectively modulates enzyme activity and oxidative stress in the testes.

TNHJPH
Funai Electric (Japan) (JP), Federal Neuro Psychiatric Hospital (NG), University of Cross River State (NG), University of Calabar (NG)
Openalex Percentile: Top 16%
Prenatal Substance Exposure Effects
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