Distinct effects of growth hormone deficiency and disruption of hypothalamic kisspeptin system on reproduction of male mice

• Published in: Life sciences (1973) 2021-11, Vol.285, p.119970-119970, Article 119970
• Main Authors: de Paula, Daniella G., Bohlen, Tabata M., Zampieri, Thais Tessari, Mansano, Naira S., Vieira, Henrique R., Gusmao, Daniela O., Wasinski, Frederick, Donato, Jose, Frazao, Renata
• Format: Article
• Language: English
• Subjects: Animal models; Arcuate nucleus; Dwarfism; Fertility; Gene expression; GH deficiency; Growth hormone-releasing hormone; Growth hormones; Hypothalamic-pituitary-gonadal axis; Hypothalamus; Immunoreactivity; Infertility; Kiss1 protein; Kisspeptin; Lesions; Males; Maturation; Metabolic imbalance; Monosodium glutamate; Mutation; Pituitary; Pituitary-gonadal axis; Puberty; Reproduction; Rodents; Sodium glutamate
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2021.119970

Growth hormone (GH) deficiency is a common cause of late sexual maturation and fertility issues. To determine whether GH-induced effects on reproduction are associated with alterations in hypothalamic kisspeptin system, we studied the male reproduction in two distinct GH deficiency mouse models. In the first model, mice present GH deficiency secondary to arcuate nucleus of the hypothalamus (ARH) lesions induced by posnatal monosodium glutamate (MSG) injections. MSG-induced ARH lesions led to significant reductions in hypothalamic Ghrh mRNA expression and consequently growth. Hypothalamic Kiss1 mRNA expression and Kiss1-expressing cells in the ARH were disrupted in the MSG-treated mice. In contrast, kisspeptin immunoreactivity remained preserved in the anteroventral periventricular and rostral periventricular nuclei (AVPV/PeN) of MSG-treated mice. Importantly, ARH lesions caused late sexual maturation and infertility in male mice. In our second mouse model, we studied animals profound GH deficiency due to a loss-of-function mutation in the Ghrhr gene (Ghrhrlit/lit mice). Interestingly, although Ghrhrlit/lit mice exhibited late puberty onset, hypothalamic Kiss1 mRNA expression and hypothalamic kisspeptin fiber density were normal in Ghrhrlit/lit mice. Despite presenting dwarfism, the majority of Ghrhrlit/lit male mice were fertile. These findings suggest that spontaneous GH deficiency during development does not compromise the kisspeptin system. Furthermore, ARH Kiss1-expressing neurons are required for fertility, while AVPV/PeN kisspeptin expression is sufficient to allow maturation of the hypothalamic-pituitary-gonadal axis in male mice. •Neonatal-induced ARH lesions compromise the kisspeptin system and the somatotropic axis.•Kisspeptin expression in the rostral hypothalamus is sufficient for HPG axis maturation.•Kisspeptin expression in the arcuate nucleus of the hypothalamus is essential for male fertility.•Growth hormone deficiency does not compromise the kisspeptin system.