LC-MS/MS quantification of a neuropeptide fragment kisspeptin-10 (NSC 741805) and characterization of its decomposition product and pharmacokinetics in rats.
Liu. Zhongfa Z; Ren. Chen C; Jones. William W; Chen. Ping P; Seminara. Stephanie B SB; Chan. Yee-Ming YM; Smith. Nicola F NF; Covey. Joseph M JM; Wang. Jeffrey J; Chan. Kenneth K KK
Key Findings
- Kisspeptin-10 degrades rapidly in plasma with half‑lives of 6.8 min at 4 °C, 2.9 min at 25 °C, and 1.7 min at 37 °C.
- The main breakdown product is the N‑terminal tyrosine‑deleted fragment (NWDSFGLRF‑NH2).
- After a 1 mg/kg IV dose in rats, kisspeptin‑10 is detectable only for a few minutes and is gone by 30 min.
Practical Outcomes
- Because kisspein‑10 is so unstable, you’d need continuous infusion or a formulation that protects it to use it effectively. Simple oral or single‑shot dosing won’t maintain levels, limiting its practical use for most biohackers.
Summary
The study shows that kisspeptin-10, a short hormone fragment that can boost reproductive hormones, breaks down very quickly in the blood of rats—only a few minutes at room temperature and disappears within half an hour after an injection. This means it’s hard to keep active long enough to have a lasting effect without special delivery methods.
Abstract
The kisspeptins are critical regulators of mammalian reproduction. Kisspeptin-10 ((45)YNWNSFGLRF-NH2(54), kisspeptin-112-121 or metastin 45-54, NSC 741805), an active fragment of kisspeptin, has been shown to be a potent stimulator of gonadotropin-releasing hormone and secretion of luteinizing hormone in both rodents and primates. This shorter peptide fragment may have clinical utility potential and it is important to characterize its pharmacokinetic property. Recently, the pharmacokinetics of both kisspeptin-54 and kisspeptin-10 were characterized in humans using a radioimmunoassay (RIA), which measures only the immunoreactive kisspeptin (kisspeptin-IR). In this study, a highly sensitive and specific LC-MS/MS assay was developed to quantify kisspeptin-10 levels in rat plasma. The lower limit of quantitation (LLOQ) was 0.5 ng/mL, the within-day and between-day coefficient of variations (CVs) ranged from 5.2 to 15.4% and 1.3 to 14.2%, and the accuracy values ranged from 98 to 114% and 99 to 105%, respectively. With this method, stability studies demonstrated that kisspeptin-10 degraded rapidly with decomposition half-lives of 6.8 min, 2.9 min and 1.7 min at 4 °C, 25 °C, and 37 °C, respectively. The principal decomposition product was characterized as the N-terminal tyrosine deleted kisspeptin-10 (46)NWDSFGLRF-NH2(54). Pharmacokinetic study in rats showed that low ng/mL kisspeptin-10 was detected in the first few minutes, and eliminated rapidly and became undetectable 30 min after intravenous (i.v.) bolus administration of 1.0 mg/kg kisspeptin-10.
Study Information
pubmed
2013
2013-03-04T00:00:00.000Z
10.1016/j.jchromb.2013.02.027
15
18