Quantification of rat kisspeptin using a novel radioimmunoassay.
Kinsey-Jones. James S JS; Beale. Kylie E KE; Cuenco. Joy J; Li. Xiao Feng XF; Bloom. Stephen R SR; O'Byrne. Kevin T KT; Murphy. Kevin G KG
Key Findings
- A radioimmunoassay (RIA) using kisspeptin-10 was developed to quantify kisspeptin protein in rodent tissues.
- Measured kisspeptin levels were 47.1 ± 6.2 fmol per hypothalamic ARC punch and 7.6 ± 1.3 fmol per AVPV punch in adult female rats.
- High‑performance liquid chromatography confirmed that the detected peptide matched synthetic kisspeptin standards.
Practical Outcomes
- For the biohacker community, this study mainly offers a new measurement tool for animal research rather than a direct protocol to use in humans. It could eventually support more precise studies on kisspeptin’s effects on metabolism or reproduction, but there are no immediate dosage or supplementation recommendations.
Summary
Scientists created a new lab test that can accurately measure the amount of the hormone kisspeptin in specific parts of a rat's brain and placenta. This helps researchers see how much of the peptide is actually present, not just how much its gene is being made.
Abstract
Kisspeptin is a hypothalamic peptide hormone that plays a pivotal role in pubertal onset and reproductive function. Previous studies have examined hypothalamic kisspeptin mRNA expression, either through in situ hybridisation or real-time RT-PCR, as a means quantifying kisspeptin gene expression. However, mRNA expression levels are not always reflected in levels of the translated protein. Kisspeptin-immunoreactivity (IR) has been extensively examined using immunohistochemistry, enabling detection and localisation of kisspeptin perikaya in the arcuate nucleus (ARC) and anteroventral periventricular nucleus (AVPV). However, quantification of kisspeptin-IR remains challenging. We developed a specific rodent radioimmunoassay assay (RIA) capable of detecting and quantifying kisspeptin-IR in rodent tissues. The RIA uses kisspeptin-10 as a standard and radioactive tracer, combined with a commercially available antibody raised to the kisspeptin-10 fragment. Adult female wistar rat brain samples were sectioned at 300 µm and the ARC and AVPV punch micro-dissected. Brain punches were homogenised in extraction buffer and assayed with rodent kisspeptin-RIA. In accord with the pattern of kisspeptin mRNA expression, kisspeptin-IR was detected in both the ARC (47.1±6.2 fmol/punch, mean±SEM n = 15) and AVPV (7.6±1.3 fmol/punch, mean±SEM n = 15). Kisspeptin-IR was also detectable in rat placenta (1.26±0.15 fmol/mg). Reverse phase high pressure liquid chromatography analysis showed that hypothalamic kisspeptin-IR had the same elution profile as a synthetic rodent kisspeptin standard. A specific rodent kisspeptin-RIA will allow accurate quantification of kisspeptin peptide levels within specific tissues in rodent experimental models.
Study Information
pubmed
2014
2014-05-20T00:00:00.000Z
10.1371/journal.pone.0097611
12
39