releasing factor

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American Heritage Dictionary:

re·leas·ing factor

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(rĭ-lē'sĭng)
n.
Any of several hormones secreted by the hypothalamus that stimulate the anterior part of the pituitary gland to release certain hormones.


A chemical factor secreted by the hypothalamus and transported to the anterior pituitary gland, where it stimulates the secretion of a particular pituitary hormone. For example, growth-hormone-releasing-factor from the hypothalamus stimulates the secretion of human growth hormone.

(rĭ-le'sĭng)
n. (Abbr. RF)

A substance of hypothalamic origin capable of accelerating the secretion of a given hormone by the anterior lobe of pituitary gland. Also called releasing hormone.

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or releasing factor

any neuropeptide synthesized in the hypothalamus that is carried to the anterior pituitary where it regulates the production and secretion of the tropic hormones, e.g. thyrotropin, somatotropin, or the gonadotropins. In the anterior pituitary releasing hormones act via the adenylate cyclase system and are then degraded by proteolysis.

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Wikipedia on Answers.com:

Releasing hormone

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A releasing hormone or releasing factor is a hormone whose main purpose is to control the release of another hormone. The main releasing hormones secreted by the hypothalamus are:

Two other factors are also classed as releasing hormones, although they in fact inhibit pituitary hormone release

For example, TRH is released from the hypothalamus in response to low levels of secretion of thyroid stimulating hormone (TSH) from the pituitary gland. The TSH in turn is under feedback control by the thyroid hormones T4 and T3. When the levels of TSH are 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.

Releasing hormones are sometimes known as liberins. For example, TRH may be known as thyroliberin. Inhibiting hormones may be known as statins. For example, dopamine (which inhibits prolactin release) may be called prolactostatin.

Contents

Mechanism

Releasing hormones increase (or, in case of inhibitory factors, decrease) the intracellular concentration of calcium (Ca2+), 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+.[1] For GHRH, however, this is a minor pathway, the main one being the cAMP dependent pathway. [2]

Notable researchers

Roger Guillemin and Andrew W. Schally were awarded the Nobel Prize in Physiology and Medicine in 1977 for their contributions to understanding "the peptide hormone production of the brain"; these scientists independently first isolated TRH and GnRH and then identified their structures.[3]

See also

References

  1. ^ Page 237 in: Costanzo, Linda S. (2007). Physiology. Hagerstwon, MD: Lippincott Williams & Wilkins. ISBN 0-7817-7311-3. 
  2. ^ Walter F., PhD. Boron (2003). Medical Physiology: A Cellular And Molecular Approaoch. Elsevier/Saunders. pp. 1300. ISBN 1-4160-2328-3. 
  3. ^ Guillemin R. Hypothalamic hormones a.k.a. hypothalamic releasing factors. J Endocrinol 2005;184:11-28. Fulltext. doi:10.1677/joe.1.05883 PMID 15642779.

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