Kisspeptin-10: The Master Regulator of Reproductive & Metabolic Research
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- Product Name: Kisspeptin-10
- Alternative Names: KISS-1, Protein KISS-1, Metastin, Kp-10 peptide
- Sequence: YNWNSFGLRF
- Molecular Formula: \(\text{C}_{63}\text{H}_{83}\text{N}_{17}\text{O}_{14}\)
- Molecular Weight: 1302.4 g/mol
- Purity: High-grade analytical specification
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- Intracellular calcium mobilization
- Arachidonic acid release
- Phosphorylation of ERK1, ERK2, and p38 MAP kinase
What is Kisspeptin-10?
Kisspeptin-10 (KP-10) is the smallest biologically active fragment of the endogenous full-length kisspeptin-145, consisting of the 10 amino acids at the C-terminus (YNWNSFGLRF-NH₂). This kisspeptin 10 peptide acts as an endogenous ligand for the G protein-coupled receptor GPR54 (also known as KISS1R). When you buy kisspeptin online, you are obtaining a compound that plays a pivotal role in the regulation of the hypothalamic-pituitary-gonadal (HPG) axis.
The kisspeptin 10 peptide is a key neurohormone that stimulates the release of gonadotropin-releasing hormone (GnRH), which in turn triggers the secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) from the pituitary gland. Research on the kisspeptin 10 peptide has revealed its diverse functions beyond reproduction, including roles in metabolism, behavior, and cancer biology.
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Understanding how does kisspeptin 10 work is fundamental to appreciating its research potential. Kisspeptin-10 exerts its effects by binding to and activating the GPR54 receptor, which is expressed in GnRH neurons in the hypothalamus. This activation triggers the pulsatile release of GnRH, which then stimulates the pituitary to release LH and FSH. The kisspeptin 10 mechanism is central to the reproductive axis, with its pulsatile secretion being critical for normal reproductive function. Interestingly, continuous administration of kisspeptin-10 can lead to tachyphylaxis (desensitization), while intermittent administration maintains its effects.
When you buy kisspeptin online, you are acquiring a powerful tool for studying the kisspeptin 10 mechanism and its role in various physiological systems.
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The kisspeptin 10 peptide benefits are wide-ranging and well-documented in scientific literature. When you buy kisspeptin online, you gain access to a compound with demonstrated potential in multiple areas of research.
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The primary kisspeptin 10 peptide benefit is its role in the regulation of the HPG axis. Research has shown that Kisspeptin-10 effectively stimulates LH release in a sexual dimorphic manner, with studies suggesting differences between males and females. In research on reproductive disorders such as infertility, amenorrhea, and pubertal delay, Kisspeptin-10 serves as a valuable tool for investigating the mechanisms underlying these conditions. When you buy kisspeptin online, you are accessing a compound that is central to understanding reproductive physiology.
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Emerging research highlights the kisspeptin 10 peptide benefits in metabolic regulation. Studies have shown that kisspeptin can modulate food intake, energy expenditure, and locomotor activity in a sexually dimorphic manner. The kisspeptin 10 peptide has also been investigated for its effects on insulin secretion, with completed Phase 3 trials exploring its action on insulin in healthy normal men and obese diabetic men. Additionally, research in rats suggests that Kisspeptin-10 may improve symptoms of gestational diabetes mellitus by suppressing insulin resistance.
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Kisspeptin-10 has been shown to influence behavioral responses. In an animal study, researchers found that Kisspeptin-10 reduced anxiety in rats, with the effect being more pronounced in males. In zebrafish, Kisspeptin-10 reduced anxiety-phobic reactions to novelty, suggesting a potential role in modulating emotional behavior. When you buy kisspeptin online, you can explore these fascinating behavioral effects in your research.
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The kisspeptin 10 peptide benefits extend to potential therapeutic applications. Research suggests that Kisspeptin-10 may have anti-tumor effects in triple-negative breast cancer, reducing cell viability and migration and inducing apoptosis. It has also been shown to prevent the development of cerebral aneurysms by reducing the expression of Egr-1. In veterinary research, Kisspeptin-10 has been evaluated for its ability to improve reproductive performance in sows in fixed-time artificial insemination programs. These diverse applications highlight the research value of Kisspeptin-10.
Kisspeptin 10 Dosage
Understanding kisspeptin 10 dosage is crucial for designing reproducible experiments. The appropriate kisspeptin 10 dosage varies based on the research model, species, and route of administration. In a safety evaluation in dogs, kisspeptin 10 dosage was administered intravenously at 30, 100, and 1000 μg/kg once daily for 14 days, with 1000 μg/kg considered the No Observed Adverse Effect Level (NOAEL).
For intranasal administration in rats, a kisspeptin 10 dosage of 0.1 mg/kg (20 μg in 20 μl) was used to study behavioral effects. In sows, kisspeptin 10 dosage of 0.5 mg and 1 mg were evaluated for effects on reproductive performance. In vitro studies have used kisspeptin 10 dosage of 12.13 nM (IC10) and 110.21 nM (IC50) in cancer cell lines.
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Kisspeptin 10 dosage for women research has been explored in various studies. A Phase 1 study evaluating the effect of exogenous kisspeptin on metabolism using a hyperglycemic clamp included women aged 18-40 with regular menstrual cycles. While specific kisspeptin 10 dosage for women data is still emerging, studies in animals suggest potential differences in response between sexes. Researchers designing studies with kisspeptin 10 dosage for women should consult primary literature for their specific model.
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Understanding kisspeptin 10 side effects is critical for responsible research. In a safety evaluation in dogs, Kisspeptin-10 demonstrated a favorable safety profile, with no observed adverse effects at doses up to 1000 μg/kg given intravenously for 14 days. However, an FDA evaluation of kisspeptin 10 side effects raised concerns about potential pro-atherosclerotic effects observed in vitro and in animal models, noting the clinical relevance remains unclear.
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