Releasing and inhibiting hormones
Releasing hormones and inhibiting hormones are hormones whose main purpose is to control the release of other hormones, either by stimulating or inhibiting their release. They are also called liberins and statins , or releasing factors and inhibiting factors. The principal examples are hypothalamic-pituitary hormones that can be classified from several viewpoints: they are hypothalamic hormones, they are hypophysiotropic hormones, and they are tropic hormones.
For example, thyrotropin-releasing hormone is released from the hypothalamus in response to low levels of secretion of thyroid-stimulating hormone from the pituitary gland. The TSH in turn is under feedback control by the thyroid hormones T4 and T3. When the level of TSH is too high, they feed back on the brain to shut down the secretion of TRH. Synthetic TRH is also used by physicians as a test of TSH reserve in the pituitary gland as it should stimulate the release of TSH and prolactin from this gland.
The main releasing hormones are as follows:
- The hypothalamus uses thyrotropin-releasing hormone to tell the pituitary to release thyrotropin.
- The hypothalamus uses corticotropin-releasing hormone to tell the pituitary to release corticotropin.
- The hypothalamus uses gonadotropin-releasing hormone to tell the pituitary to release gonadotropin.
- The hypothalamus uses growth hormone–releasing hormone to tell the pituitary to release somatotropin.
- The hypothalamus uses somatostatin to tell the pituitary to inhibit somatotropin and to tell the gastrointestinal tract to inhibit various gastrointestinal hormones.
- The hypothalamus uses dopamine as a prolactostatin to tell the pituitary to inhibit prolactin; it is also created elsewhere in the brain and the adrenal cortex as a neurotransmitter to affect many other systems.
- The hypothalamus uses RFRP-3 in mammals or GnIH in avian species to inhibit GnRH.
- The hypothalamus uses follistatin to tell the pituitary to inhibit follicle-stimulating hormone; it also has many other systemic effects.
- Myocytes use myostatin to tell each other to inhibit myogenesis.
- Melanocyte-inhibiting factor inhibits release of other neuropeptides such as alpha-MSH and also has many other functions.
- There is a neuropeptide called cortistatin and a class of steroidal cortistatins.
Mechanism
Releasing hormones increase the intracellular concentration of calcium, resulting in vesicle fusion of the respective primary hormone.For GnRH, TRH and GHRH the increase in Ca2+ is achieved by the releasing hormone coupling and activating G protein [coupled receptors] coupled to the Gq alpha subunit, activating the IP3/DAG pathway to increase Ca2+. For GHRH, however, this is a minor pathway, the main one being the cAMP dependent pathway.