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Manipulating seasonality by using PMSG and Kisspeptin hormones and the impact of the MTNR1A gene on reproduction efficiency in ewes.

BACKGROUND: One of the most important problems in sheep is seasonal anestrus, which limits the reproductive efficiency of the sheep. Estrous synchronization is considered the first plan for reproductive performance in sheep due to the pregnancy time is limited, and parturition as well as an increase in twining and reached good genetic characteristics. AIM: This study aimed to manipulate seasonality that limits fertility in ewes by induction estrus during seasonal anestrous in sheep by using Pregnant Mare Serum Gonadotropin (PMSG), Kisspeptin hormone, and study the impact of MTNR1A gene on reproduction efficiency in ewes. METHODS: This study examined 36 Awassi ewes divided into two groups, each containing 18 ewes, 2-3 years old, and two fertile rams aged 3-4 years and weighing 60-65 kg. All non-pregnant ewes were synchronized using vaginal sponges (60 mg Medroxy Progesterone acetate) for 10 days. The injection of treatment when sponges are draws. The first group (G1) received 500 IU of PMSG injection, and the second group (G2) injection a Kisspeptin hormone 5 &#x3bc;g/kg B.W. RESULTS: The results showed the G1 treated by PMSG 500IU were higher significantly (p &#x2264; 0.05) of estrus response, induction estrus and pregnancy (89%, 89%, and 89%), respectively, comparative with G2 treated by (Kisspeptin 5 mg/kg) were (72%, 72%, and 66%), respectively, and non-significant changes in estrus were observed in all groups. The average peripheral progesterone concentration significantly increased from day 0 to 5th month in G1 comparative with G2 in pregnant ewes. Serum progesterone levels were significantly p < 0.05 during of 4th month in G1 treatment by (PMSG 500IU) compared with day 0 and all other months during pregnancy of ewes. The average days to lambing in genotypes CT and TT (150 &#xb1; 2.5 and 152 &#xb1; 3.5 days), respectively, were significant comparative with CC genotype; however, the litter size and lambing rate observed in the enrolled ewes were non-significant in all genotypes. CC, CT, and TT represent three possible genotypes at a specific location (locus) in the genome, often referring to a single nucleotide polymorphism (SNP). These genotypes indicate the combination of alleles an individual inherits from their parents for a particular gene. They refer to the presence of two alleles for a particular nitrogenous base: C and T are nitrogenous bases: C = Cytosine and T = Thymine. CONCLUSION: In conclusion, the application of PMSG and Kisspeptin was effective in achievement good higher significantly of reproduction efficiency in this study. The genotypes CT and TT of the MTNR1A gene polymorphism were connected with a short significant of days to lambing in genotypes.

Animals

Polycystic ovary syndrome and idiopathic central precocious puberty: two sides of the same coin?

PURPOSE: Several studies have reported an association between central precocious puberty (CPP) and a higher prevalence of polycystic ovary syndrome (PCOS), raising the hypothesis that CPP may act as an early-life indicator of increased PCOS risk. This review investigates the shared genetic, epigenetic, and environmental factors potentially underlying CPP and PCOS, with the aim of clarifying their connection and supporting advances in early detection and management. METHODS: A comprehensive literature review was conducted using the PubMed/MEDLINE database, prioritizing research from the past two decades, supplemented by key studies from earlier years. This research included studies on genetic and epigenetic factors, endocrine-disrupting chemicals (EDCs), and metabolic influences related to CPP and PCOS. Both original research and review articles were selected, focusing on the identification of pathophysiological mechanisms and risk factors linking these disorders. RESULTS: Genome-wide association studies (GWAS) have linked genetic variants in the kisspeptin and neurokinin B signaling pathways to increased gonadotropin-releasing hormone (GnRH) secretion, triggering early puberty. Moreover, increased GnRH pulsatility contributes to elevated luteinizing hormone (LH) levels, altered LH/follicle-stimulating hormone (FSH) ratios, and ovarian hyperandrogenism&#x2014;key pathophysiological features of PCOS. Additionally, epigenetic modifications, particularly changes in DNA methylation at CpG sites, have been observed in both CPP and PCOS. A hyperandrogenic intrauterine environment and inadequate fetal growth contribute to prenatal epigenetic alterations, while postnatal factors such as obesity, insulin resistance, and exposure to EDCs further influence epigenetic modifications. Although insulin resistance and hyperandrogenism are central features linking CPP to PCOS, the precise mechanisms underlying these associations remain complex and not yet fully elucidated. CONCLUSIONS: Identifying shared genetic and environmental factors influencing early puberty onset and PCOS highlights the importance of close clinical monitoring in early life, though preventive interventions remain unproven. Further research is needed to clarify these mechanisms, which will support the development of more precise prevention and treatment strategies in clinical practice.

Humans