Phoenixin Attenuates Monosodium Glutamate-Induced Testicular Toxicity in Rats: A Potential Protective Approach

Background: Monosodium glutamate (MSG), a widely utilized food additive, has been implicated in the provocation of testicular toxicity through oxidative stress and hormonal dysregulation.Aim: This study explores the potential role of phoenixin in ameliorating MSG-persuaded testicular toxicity. Methods: The Experimental design involved allocating male Wistar rats into four distinct groups: Control, Phoenixin, MSG, and Phoenixin+ MSG. Semen samples were analyzed for sperm count, motility, and viability. Gonadotropin-releasing hormone.(GnRH). In serum, luteinizing hormone (LH), follicle-stimulating hormone (FSH), testosterone, and kisspeptin were quantitatively assessed. The activity of the testicular steroidogenic enzymes 3β-hydroxysteroid dehydrogenase (3β-HSD) and 17β-HSD, together with markers of testicular oxidative stress and tumor necrosis factor-alpha (TNF-α), were assessed. Additionally, the testicular levels of silent information.regulator.of/transcription.1(SIRT1), phosphorylated AMP-activated protein kinase (p-AMPK), and caspase3 immunoreactivity were estimated.Results: MSG exposure significantly impaired sperm parameters, disrupted hormonal balance, and triggered oxidative stress and inflammatory responses. Meanwhile, co-administration of phoenixin restored sperm function, improved serum GnRH, LH, FSH, testosterone, and kisspeptin levels, and enhanced testicular antioxidant defense. Moreover, phoenixin upregulated p-AMPK and SIRT1 while attenuating TNF-α expression and caspase3 immunoreactivity, elucidating its beneficial role in mitigating testicular function and steroidogenesis.Conclusion: Phoenixin effectively protected against MSG-provoked testicular toxicity through the restoration of the hypothalamic-pituitary-gonadal(HPG), enhancement of steroidogenesis, attenuation of oxidative stress, inflammation, and apoptotic cascade, which was enforced by its upregulation to the SIRT1/AMPK signaling. These results imply a beneficial role of phoenixin in mitigating the reproductive dysfunction associated with MSG testicular toxicity.Keywords: Phoenixin, Monosodium Glutamate, Testicular Toxicity.

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Journal
Bulletin of Egyptian Society for Physiological Sciences
Published
2025-10-01
DOI
https://doi.org/10.21608/besps.2025.374725.1210
Primary Topic
Biochemical Analysis and Sensing Techniques
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article
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article

Phoenixin Attenuates Monosodium Glutamate-Induced Testicular Toxicity in Rats: A Potential Protective Approach

Heba Mamdoh Shoeib, Mohamed Azab, Islam Ibrahim Hegab, Asmaa Mohamed et al.
Bulletin of Egyptian Society for Physiological Sciences
Biochemical Analysis and Sensing Techniques
article

Phoenixin Attenuates Monosodium Glutamate-Induced Testicular Toxicity in Rats: A Potential Protective Approach

Heba Mamdoh Shoeib, Mohamed Azab, Islam Ibrahim Hegab, Asmaa Mohamed, nancy Abed El-Hady, nesren mohamed aboadra
article en

Abstract

Background: Monosodium glutamate (MSG), a widely utilized food additive, has been implicated in the provocation of testicular toxicity through oxidative stress and hormonal dysregulation.Aim: This study explores the potential role of phoenixin in ameliorating MSG-persuaded testicular toxicity. Methods: The Experimental design involved allocating male Wistar rats into four distinct groups: Control, Phoenixin, MSG, and Phoenixin+ MSG. Semen samples were analyzed for sperm count, motility, and viability. Gonadotropin-releasing hormone.(GnRH). In serum, luteinizing hormone (LH), follicle-stimulating hormone (FSH), testosterone, and kisspeptin were quantitatively assessed. The activity of the testicular steroidogenic enzymes 3β-hydroxysteroid dehydrogenase (3β-HSD) and 17β-HSD, together with markers of testicular oxidative stress and tumor necrosis factor-alpha (TNF-α), were assessed. Additionally, the testicular levels of silent information.regulator.of/transcription.1(SIRT1), phosphorylated AMP-activated protein kinase (p-AMPK), and caspase3 immunoreactivity were estimated.Results: MSG exposure significantly impaired sperm parameters, disrupted hormonal balance, and triggered oxidative stress and inflammatory responses. Meanwhile, co-administration of phoenixin restored sperm function, improved serum GnRH, LH, FSH, testosterone, and kisspeptin levels, and enhanced testicular antioxidant defense. Moreover, phoenixin upregulated p-AMPK and SIRT1 while attenuating TNF-α expression and caspase3 immunoreactivity, elucidating its beneficial role in mitigating testicular function and steroidogenesis.Conclusion: Phoenixin effectively protected against MSG-provoked testicular toxicity through the restoration of the hypothalamic-pituitary-gonadal(HPG), enhancement of steroidogenesis, attenuation of oxidative stress, inflammation, and apoptotic cascade, which was enforced by its upregulation to the SIRT1/AMPK signaling. These results imply a beneficial role of phoenixin in mitigating the reproductive dysfunction associated with MSG testicular toxicity.Keywords: Phoenixin, Monosodium Glutamate, Testicular Toxicity.

Bulletin of Egyptian Society for Physiological SciencesVol. 45(4)
Tanta University (EG), Ibn Sina National College for Medical Studies (SA)
Openalex Percentile: Top 66%
Biochemical Analysis and Sensing Techniques
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