{"title":"Nicotinamide mononucleotide enhances porcine sperm quality by activating the SIRT3-SOD2/ROS pathway and promoting oxidative phosphorylation","authors":"Haize Zhang, Xue Qin, Nataraj Bojan, Chaoyue Cao, Jiawen Chai, Weijun Pang","doi":"10.1016/j.anireprosci.2025.107797","DOIUrl":null,"url":null,"abstract":"<div><div>Sperm quality is crucial for animal reproduction but is often deteriorates due to oxidative stress. Preserving functionality during storage by protecting it from oxidative stress is crucial for enhancing the success of assisted reproductive technologies and maintaining fertility. Nicotinamide mononucleotide (<strong>NMN</strong>), a precursor of Nicotinamide adenine dinucleotide (<strong>NAD</strong><sup><strong>+</strong></sup>), acts as a potent antioxidant. However, its role and regulatory mechanism in porcine sperm liquid preservation <em>in vitro</em> are remains unclear. In this study we demonstrated that NMN supplementation in the semen diluent significantly improved porcine sperm quality during storage at 17 °C by increasing NAD<sup>+</sup> concentrations and decreasing the reactive oxygen species (<strong>ROS</strong>) concentrations in sperm. Subsequent analysis revealed that NMN, upon conversion to NAD<sup>+</sup> within sperm, exerted antioxidant effect by upregulating the mitochondrial protein sirtuin 3 (<strong>SIRT3</strong>), resulting in the downregulation of superoxide dismutase 2 (<strong>SOD2</strong>) acetylation. This pathway mitigated oxidative stress. Additionally, NMN also enhanced sperm oxidative phosphorylation (<strong>OXPHOS</strong>) thereby increase adenosine triphosphate (<strong>ATP</strong>) production concentrations via activating SIRT3, without affecting sperm glycolysis. Furthermore, the semen diluent supplemented with 50 μg/mL NMN resulted in improved reproductive outcomes, including the birth of healthier piglets and a reduction in stillbirths rates following artificial insemination (<strong>AI</strong>). Taken together, NMN improves porcine sperm quality through SIRT3-activating the SOD2/ROS axis and oxidative phosphorylation. Our findings advance understanding of sperm physiology and metabolism and provide a new avenue promising approach for developing innovative semen diluents for liquid preservation in animal reproduction biology <em>in vitro.</em></div></div>","PeriodicalId":7880,"journal":{"name":"Animal Reproduction Science","volume":"275 ","pages":"Article 107797"},"PeriodicalIF":2.2000,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal Reproduction Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378432025000363","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Sperm quality is crucial for animal reproduction but is often deteriorates due to oxidative stress. Preserving functionality during storage by protecting it from oxidative stress is crucial for enhancing the success of assisted reproductive technologies and maintaining fertility. Nicotinamide mononucleotide (NMN), a precursor of Nicotinamide adenine dinucleotide (NAD+), acts as a potent antioxidant. However, its role and regulatory mechanism in porcine sperm liquid preservation in vitro are remains unclear. In this study we demonstrated that NMN supplementation in the semen diluent significantly improved porcine sperm quality during storage at 17 °C by increasing NAD+ concentrations and decreasing the reactive oxygen species (ROS) concentrations in sperm. Subsequent analysis revealed that NMN, upon conversion to NAD+ within sperm, exerted antioxidant effect by upregulating the mitochondrial protein sirtuin 3 (SIRT3), resulting in the downregulation of superoxide dismutase 2 (SOD2) acetylation. This pathway mitigated oxidative stress. Additionally, NMN also enhanced sperm oxidative phosphorylation (OXPHOS) thereby increase adenosine triphosphate (ATP) production concentrations via activating SIRT3, without affecting sperm glycolysis. Furthermore, the semen diluent supplemented with 50 μg/mL NMN resulted in improved reproductive outcomes, including the birth of healthier piglets and a reduction in stillbirths rates following artificial insemination (AI). Taken together, NMN improves porcine sperm quality through SIRT3-activating the SOD2/ROS axis and oxidative phosphorylation. Our findings advance understanding of sperm physiology and metabolism and provide a new avenue promising approach for developing innovative semen diluents for liquid preservation in animal reproduction biology in vitro.
期刊介绍:
Animal Reproduction Science publishes results from studies relating to reproduction and fertility in animals. This includes both fundamental research and applied studies, including management practices that increase our understanding of the biology and manipulation of reproduction. Manuscripts should go into depth in the mechanisms involved in the research reported, rather than a give a mere description of findings. The focus is on animals that are useful to humans including food- and fibre-producing; companion/recreational; captive; and endangered species including zoo animals, but excluding laboratory animals unless the results of the study provide new information that impacts the basic understanding of the biology or manipulation of reproduction.
The journal''s scope includes the study of reproductive physiology and endocrinology, reproductive cycles, natural and artificial control of reproduction, preservation and use of gametes and embryos, pregnancy and parturition, infertility and sterility, diagnostic and therapeutic techniques.
The Editorial Board of Animal Reproduction Science has decided not to publish papers in which there is an exclusive examination of the in vitro development of oocytes and embryos; however, there will be consideration of papers that include in vitro studies where the source of the oocytes and/or development of the embryos beyond the blastocyst stage is part of the experimental design.