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Article Abstract

Leydig cells (LCs) play a pivotal role in male fertility, producing testosterone. Chromium (III) picolinate (CrPic), a contentious supplement with antidiabetic and antioxidant properties, raises concerns regarding male fertility. Using a rodent LC line, we investigated the cytotoxicity of increasing CrPic doses. An insulin resistance (IR) model was established using palmitate (PA), and LCs were further exposed to CrPic to assess its antioxidant/antidiabetic activities. An exometabolome analysis was performed using H-NMR. Mitochondrial function and oxidative stress were evaluated via immunoblot. Steroidogenesis was assessed by quantifying androstenedione through ELISA. Our results uncover the toxic effects of CrPic on LCs even at low doses under IR conditions. Furthermore, even under these IR conditions, CrPic fails to enhance glucose consumption but restores the expression of mitochondrial complexes CII and CIII, alleviating oxidative stress in LCs. While baseline androgen production remained unaffected, CrPic promoted androstenedione production in LCs in the presence of PA, suggesting that it promotes cholesterol conversion into androgenic intermediates in this context. This study highlights the need for caution with CrPic even at lower doses. It provides valuable insights into the intricate factors influencing LCs metabolism and antioxidant defenses, shedding light on potential benefits and risks of CrPic, particularly in IR conditions.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10812815PMC
http://dx.doi.org/10.3390/antiox13010040DOI Listing

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