Caloric restriction alters the hormonal profile and testicular metabolome, resulting in alterations of sperm head morphology.
Ana D MartinsIvana JarakTiago MoraisRui A CarvalhoPedro F OliveiraMariana P MonteiroMarco G AlvesPublished in: American journal of physiology. Endocrinology and metabolism (2019)
Energy homeostasis is crucial for all physiological processes. Thus, when there is low energy intake, negative health effects may arise, including in reproductive function. We propose to study whether caloric restriction (CR) changes testicular metabolic profile and ultimately sperm quality. Male Wistar rats (n = 12) were randomized into a CR group fed with 30% fewer calories than weight-matched, ad libitum-fed animals (control group). Circulating hormonal profile, testicular glucagon-like peptide-1 (GLP-1), ghrelin and leptin receptors expression, and sperm parameters were analyzed. Testicular metabolite abundance and glycolysis-related enzymes were studied by NMR and Western blot, respectively. Oxidative stress markers were analyzed in testicular tissue and spermatozoa. Expressions of mitochondrial complexes and mitochondrial biogenesis in testes were determined. CR induced changes in body weight along with altered GLP-1, ghrelin, and leptin circulating levels. In testes, CR led to changes in receptor expression that followed those of the hormone levels; modified testicular metabolome, particularly amino acid content; and decreased oxidative stress-induced damage in testis and spermatozoa, although sperm head defects increased. In sum, CR induced changes in body weight, altering circulating hormonal profile and testicular metabolome and increasing sperm head defects. Ultimately, our data highlight that conditions of CR may compromise male fertility.
Keyphrases
- germ cell
- body weight
- oxidative stress
- amino acid
- polycystic ovary syndrome
- dna damage
- poor prognosis
- body mass index
- adipose tissue
- weight gain
- deep learning
- metabolic syndrome
- randomized controlled trial
- ischemia reperfusion injury
- electronic health record
- mass spectrometry
- binding protein
- artificial intelligence
- young adults
- phase ii
- antibiotic resistance genes