GnRH (Gonadotropin-Releasing Hormone)
Definition
The hypothalamic hormone released in pulses that tells the pituitary to secrete luteinising hormone and follicle-stimulating hormone. Continuous rather than pulsatile stimulation of its receptor has the opposite effect and shuts those hormones down.
Terms used in this definition
Other entries this definition refers to.
Where this term comes up
Entries whose definition mentions GnRH (Gonadotropin-Releasing Hormone).
What this means for research sourcing
Mechanistic terms like this describe how research compounds behave in vitro. See the mechanism overviews for compounds Volta stocks.
Related Terms in Pharmacology
Luteinizing Hormone (LH)
A pituitary gonadotropin that triggers ovulation and, in males, drives testosterone production by testicular Leydig cells. HCG is used in research as an LH analogue because it acts at the same receptor with a longer half-life.
Follicle-Stimulating Hormone (FSH)
The other pituitary gonadotropin, which supports ovarian follicle development and spermatogenesis. It is released alongside LH under GnRH control, and the two are usually measured together.
Cortisol
The adrenal glucocorticoid released under stress and on a daily rhythm. It is measured in growth hormone secretagogue studies because some compounds in that class raise it transiently while others do not, and that difference is what selectivity means here.
Prolactin
A pituitary hormone best known for its role in lactation, also measured in secretagogue studies because several GHRPs raise it modestly. Ipamorelin's reputation rests largely on not doing so.
Oxytocin
A nine-residue hypothalamic peptide released from the posterior pituitary, involved in uterine contraction, milk ejection and a range of social behaviours studied in animal models. It is one of the few peptides with a substantial body of work in the literature using an intranasal route.
Vasopressin
A nine-residue posterior-pituitary peptide, also called antidiuretic hormone, that governs water retention by the kidney and raises vascular tone. It differs from oxytocin at two residues, which is a standard illustration of how much a single substitution changes.
Melanocortin Receptor
A family of five G protein-coupled receptors, MC1R through MC5R, covering pigmentation, sexual function, appetite and inflammation. Which subtype a compound prefers is what distinguishes the melanocortin peptides from one another.
PepT1 Transporter
The proton-coupled transporter SLC15A1 in the intestinal epithelium, which carries di- and tripeptides across intact. It is the one established route by which a very short oral peptide can be absorbed without being broken down first; longer chains cannot use it.