{"title":"短沟通:在合作繁殖的啮齿动物中,睾酮水平升高与先天免疫功能增强有关","authors":"K.M.E. Wallace , S.N. Venter , N.C. Bennett , D.W. Hart","doi":"10.1016/j.cbpa.2025.111911","DOIUrl":null,"url":null,"abstract":"<div><div>In many vertebrates, elevated testosterone is believed to compromise the immune function, reflecting a trade-off between reproduction and survival. However, such trade-offs may potentially be relaxed in cooperative breeders, where social conflict and sexual selection are reduced. We investigated the relationship between testosterone, cortisol, and innate immunity in captive male Damaraland mole-rats (<em>Fukomys damarensis</em>), a eusocial rodent with minimal aggression-driven reproductive competition. Using microbial killing assays (MKAs) and white blood cell counts as proxies of immune function, we found that urinary testosterone concentration was positively correlated with immune strength. Males with higher urinary testosterone concentrations exhibited significantly greater antimicrobial capacity and elevated total white blood cell counts. However, urinary testosterone was unrelated to independent immune cell differentials. While, reproductive status, age, body mass, and urinary cortisol concentrations had a limited effect on any immune metric. These findings, while correlative, challenge traditional endocrine-immune trade-off models and infer that, in this species, testosterone may signal condition rather than impose immunosuppressive costs.</div></div>","PeriodicalId":55237,"journal":{"name":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","volume":"308 ","pages":"Article 111911"},"PeriodicalIF":2.2000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Short communication: Elevated testosterone correlates with enhanced innate immune function in a cooperatively breeding rodent\",\"authors\":\"K.M.E. Wallace , S.N. Venter , N.C. Bennett , D.W. Hart\",\"doi\":\"10.1016/j.cbpa.2025.111911\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In many vertebrates, elevated testosterone is believed to compromise the immune function, reflecting a trade-off between reproduction and survival. However, such trade-offs may potentially be relaxed in cooperative breeders, where social conflict and sexual selection are reduced. We investigated the relationship between testosterone, cortisol, and innate immunity in captive male Damaraland mole-rats (<em>Fukomys damarensis</em>), a eusocial rodent with minimal aggression-driven reproductive competition. Using microbial killing assays (MKAs) and white blood cell counts as proxies of immune function, we found that urinary testosterone concentration was positively correlated with immune strength. Males with higher urinary testosterone concentrations exhibited significantly greater antimicrobial capacity and elevated total white blood cell counts. However, urinary testosterone was unrelated to independent immune cell differentials. While, reproductive status, age, body mass, and urinary cortisol concentrations had a limited effect on any immune metric. These findings, while correlative, challenge traditional endocrine-immune trade-off models and infer that, in this species, testosterone may signal condition rather than impose immunosuppressive costs.</div></div>\",\"PeriodicalId\":55237,\"journal\":{\"name\":\"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology\",\"volume\":\"308 \",\"pages\":\"Article 111911\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-07-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1095643325001102\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology A-Molecular & Integrative Physiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1095643325001102","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Short communication: Elevated testosterone correlates with enhanced innate immune function in a cooperatively breeding rodent
In many vertebrates, elevated testosterone is believed to compromise the immune function, reflecting a trade-off between reproduction and survival. However, such trade-offs may potentially be relaxed in cooperative breeders, where social conflict and sexual selection are reduced. We investigated the relationship between testosterone, cortisol, and innate immunity in captive male Damaraland mole-rats (Fukomys damarensis), a eusocial rodent with minimal aggression-driven reproductive competition. Using microbial killing assays (MKAs) and white blood cell counts as proxies of immune function, we found that urinary testosterone concentration was positively correlated with immune strength. Males with higher urinary testosterone concentrations exhibited significantly greater antimicrobial capacity and elevated total white blood cell counts. However, urinary testosterone was unrelated to independent immune cell differentials. While, reproductive status, age, body mass, and urinary cortisol concentrations had a limited effect on any immune metric. These findings, while correlative, challenge traditional endocrine-immune trade-off models and infer that, in this species, testosterone may signal condition rather than impose immunosuppressive costs.
期刊介绍:
Part A: Molecular & Integrative Physiology of Comparative Biochemistry and Physiology. This journal covers molecular, cellular, integrative, and ecological physiology. Topics include bioenergetics, circulation, development, excretion, ion regulation, endocrinology, neurobiology, nutrition, respiration, and thermal biology. Study on regulatory mechanisms at any level of organization such as signal transduction and cellular interaction and control of behavior are also published.