Vega Aurélie, Martinot Emmanuelle, Baptissart Marine, De Haze Angélique, Vaz Frederic, Kulik Wim, Damon-Soubeyrand Christelle, Baron Silvère, Caira Françoise, Volle David H
INSERM U 1103, Génétique Reproduction et Développement (GReD), F-63178 Aubière, France; Université Clermont Auvergne, GReD, F-63178 Aubière, France; CNRS, UMR 6293, GReD, F-63178 Aubière, France; Centre de Recherche en Nutrition Humaine d'Auvergne, F-63000 Clermont-Ferrand, France.
Academic Medical Center, University of Amsterdam, Lab. Genetic Metabolic Diseases, F0-224, P.O. Box 22700, 1100 DE Amsterdam, The Netherlands.
PLoS One. 2015 Oct 6;10(10):e0139946. doi: 10.1371/journal.pone.0139946. eCollection 2015.
Bile acids have recently been demonstrated as molecules with endocrine activities controlling several physiological functions such as immunity and glucose homeostases. They act mainly through two receptors, the nuclear receptor Farnesol-X-Receptor alpha (FXRα) and the G-protein coupled receptor (TGR5). These recent studies have led to the idea that molecules derived from bile acids (BAs) and targeting their receptors must be good targets for treatment of metabolic diseases such as obesity or diabetes. Thus it might be important to decipher the potential long term impact of such treatment on different physiological functions. Indeed, BAs have recently been demonstrated to alter male fertility. Here we demonstrate that in mice with overweight induced by high fat diet, BA exposure leads to increased rate of male infertility. This is associated with the altered germ cell proliferation, default of testicular endocrine function and abnormalities in cell-cell interaction within the seminiferous epithelium. Even if the identification of the exact molecular mechanisms will need more studies, the present results suggest that both FXRα and TGR5 might be involved. We believed that this work is of particular interest regarding the potential consequences on future approaches for the treatment of metabolic diseases.
胆汁酸最近被证明是具有内分泌活性的分子,可控制多种生理功能,如免疫和葡萄糖稳态。它们主要通过两种受体发挥作用,即核受体法尼醇X受体α(FXRα)和G蛋白偶联受体(TGR5)。这些最新研究引发了这样一种观点,即源自胆汁酸(BAs)并靶向其受体的分子必定是治疗肥胖或糖尿病等代谢性疾病的良好靶点。因此,解读这种治疗对不同生理功能的潜在长期影响可能很重要。事实上,最近已证明胆汁酸会改变男性生育能力。在此我们证明,在高脂肪饮食诱导超重的小鼠中,接触胆汁酸会导致男性不育率增加。这与生殖细胞增殖改变、睾丸内分泌功能缺陷以及生精上皮内细胞间相互作用异常有关。即便确定确切的分子机制还需要更多研究,但目前的结果表明FXRα和TGR5可能都参与其中。我们认为这项工作对于代谢性疾病未来治疗方法的潜在后果具有特别重要的意义。