Dena Simon Mwaringa, Adeleye Adesola Oluwaseun, Mohlala Kutullo, Langa Bridget Cebisile, Opuwari Chinyerum Sylvia
Department of Medical Biosciences, Faculty of Natural Sciences, University of the Western Cape, Cape Town, South Africa.
J Diabetes. 2025 Oct;17(10):e70157. doi: 10.1111/1753-0407.70157.
Diabetes mellitus (DM) significantly impairs male reproductive health, largely through hyperglycemia-induced oxidative stress (OS). Elevated glucose activates detrimental metabolic pathways, notably the polyol pathway, which depletes antioxidant defenses and generates reactive oxygen species (ROS). This oxidative burden damages spermatozoa, leading to reduced motility, abnormal morphology, DNA fragmentation, and disrupted membrane integrity. OS also compromises the hypothalamic-pituitary-gonadal axis, lowering testosterone synthesis and impairing spermatogenesis. The formation of advanced glycation end products (AGEs) and chronic inflammation further exacerbate Leydig and Sertoli cell dysfunction, microvascular injury, and testicular apoptosis. Clinical evidence consistently links DM to deteriorated semen parameters, hormonal imbalances, and reduced natural conception rates, with poorer outcomes in assisted reproductive technologies. Obesity and metabolic syndrome, common comorbidities in DM, amplify oxidative stress and further impair fertility potential. While seminal plasma contains enzymatic and non-enzymatic antioxidants, these defenses are often insufficient in diabetic men. Targeted interventions, including antioxidant therapy, lifestyle modifications, glycemic control, and management of comorbidities, offer promise in mitigating oxidative damage. This review synthesizes current evidence on the molecular, endocrine, and clinical consequences of DM-related oxidative stress on male fertility, underscoring the need for integrated management strategies to preserve reproductive function in diabetic men.
糖尿病(DM)会显著损害男性生殖健康,主要是通过高血糖诱导的氧化应激(OS)。血糖升高会激活有害的代谢途径,尤其是多元醇途径,该途径会耗尽抗氧化防御并产生活性氧(ROS)。这种氧化负担会损害精子,导致精子活力降低、形态异常、DNA碎片化以及膜完整性受损。氧化应激还会损害下丘脑 - 垂体 - 性腺轴,降低睾酮合成并损害精子发生。晚期糖基化终产物(AGEs)的形成和慢性炎症会进一步加剧睾丸间质细胞和支持细胞功能障碍、微血管损伤以及睾丸细胞凋亡。临床证据始终将糖尿病与精液参数恶化、激素失衡以及自然受孕率降低联系起来,在辅助生殖技术中结果更差。肥胖和代谢综合征是糖尿病常见的合并症,会加剧氧化应激并进一步损害生育潜力。虽然精浆含有酶类和非酶类抗氧化剂,但这些防御在糖尿病男性中往往不足。有针对性的干预措施,包括抗氧化治疗、生活方式改变、血糖控制以及合并症管理,有望减轻氧化损伤。本综述综合了当前关于糖尿病相关氧化应激对男性生育力的分子、内分泌和临床后果的证据,强调需要综合管理策略来保护糖尿病男性的生殖功能。