Male rhesus monkeys secrete adult levels of androgen for 3 months postnatally. The role of this neonatal testicular secretion in sexual development was investigated by suppressing luteinizing hormone (LH) and testosterone (T) in neonatal male rhesus (n = 6) by administering a gonadotropin-releasing hormone agonist (Ag) for the first 4 months of postnatal life. Controls (n = 4) received vehicle. Six years later, endocrine function and sexual behavior were examined with ovariectomized females (n = 6) receiving periodic estradiol (E2) treatment during the breeding and nonbreeding seasons. During the breeding season, there were no differences between Ag-treated and control males in levels of LH and T or in frequency of copulatory behavior. However, Ag-treated males masturbated less frequently than controls when the females were not on E2. During the nonbreeding season, Ag-treated males had lower T levels than controls when the females were not receiving E2 and copulated less when the females received E2, even though T levels were comparable. During both E2 and non-E2 treatments, Ag-treated males secreted less T per unit of LH than controls. Neonatal Ag treatment had no effect on social rank. These data demonstrate that neonatal testicular suppression, or the Ag treatment itself, altered systems regulating sexual motivation and neuroendocrine control of these males and suggest that the early neonatal period in male rhesus monkeys is another point when the developing central nervous system is sensitive to the organizing actions of androgens.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1006/hbeh.1993.1040 | DOI Listing |
Stem Cell Res Ther
January 2025
Department of Anatomical Sciences, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Background: Culture medium enriched with Knockout serum replacement (KSR) can produce in vitro mouse sperm, but it is inefficient, strain-specific and contains bovine products, which limits its use in the human clinic. The study aimed to optimize the culture medium for testicular tissue by using plasma rich in growth factors (PRGF) as a serum supplement, addressing the limitations of KSR.
Methods: Immature testicular tissues from NMRI mice were cultured for 14 days to identify the optimal PRGF concentration using histological analysis and tubular integrity scoring.
BMC Genomics
January 2025
Key Laboratory of Adaptation and Evolution of Plateau Biota, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, Qinghai, 810008, China.
Background: Spermatogonia are essential for the continual production of sperm and regeneration of the entire spermatogenic lineage after injury. In mammals, spermatogonia are formed in the neonatal testis from prospermatogonia (also termed gonocytes), which are established from primordial germ cells during fetal development. Currently, the molecular regulation of the prospermatogonial to spermatogonia transition is not fully understood.
View Article and Find Full Text PDFJBRA Assist Reprod
January 2025
Department of Anatomical Sciences, Faculty of Medicine, Tarbiat Modares University, Tehran, Iran.
Objective: Many cancer survivors may experience irreversible infertility due to chemotherapy treatment for childhood cancer. In this study, spermatogenesis development was evaluated following the grafting of fresh and frozen-thawed testicular tissue from neonatal mice to the epididymal fat of adult mice.
Methods: After bilateral castration of recipient mice, fresh or frozen-thawed neonatal testis tissues were grafted into the epididymal fat of the mice.
Chem Res Toxicol
January 2025
Department of Anesthesiology and Perioperative Medicine, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325027, China.
Perfluorodecanoic acid (PFDA), a C10 fluorine-containing compound, is used widely and found to be present anywhere. However, whether it has reproductive toxicity for fetal Leydig cells and the underlying mechanisms remain unknown. PFDA was investigated for its effects on fetal Leydig cells (FLCs) following exposure to 0, 1, 2.
View Article and Find Full Text PDFTurk J Pediatr
November 2024
Division of Pediatric Immunology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
Background: Griscelli syndrome (GS) is a rare genetic disorder characterized by oculocutaneous albinism and variable immune dysfunction. Among three distinct types of GS, occurring due to different genetic mutations; GS type 1 presents with neurological manifestations, hemophagocytic lymphohistiocytosis (HLH) generally develops in GS type 2, and GS type 3 primarily exhibits oculocutaneous albinism. HLH, a life-threatening condition with excessive immune activation, may occur secondary to various triggers, including infections, and develop in different tissues, as well as in the testis, similar to Erdheim-Chester disease.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!