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Anterior pituitary

From Wikipedia, the free encyclopedia
Anterior lobe of the pituitary gland
Anterior pituitary gland
Diagram of anterior lobe of the pituitary, and its sections shown with the posterior lobe
Details
PrecursorOral mucosa (Rathke's pouch)
ArterySuperior hypophyseal
VeinHypophyseal
Identifiers
Latinlobus anterior hypophysis
MeSHD010903
NeuroNames407
NeuroLex IDbirnlex_1581
TA98A11.1.00.002
TA23855
FMA74627
Anatomical terminology

Theanterior pituitary (also called theadenohypophysis orpars anterior) is a majororgan of theendocrine system. The anterior pituitary is theglandular,anterior lobe that together with theposterior pituitary (or neurohypophysis) makes up thepituitary gland (hypophysis) which, inhumans, is located at the base of thebrain, protruding off the bottom of thehypothalamus.

The anterior pituitary regulates severalphysiological processes, includingstress,growth,reproduction, andlactation. Proper functioning of the anterior pituitary and of the organs it regulates can often be ascertained viablood tests that measurehormone levels.

Structure

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The anterior pituitary complex

Thepituitary gland sits in a protective bony enclosure called thesella turcica (Turkish chair/saddle). It is composed of three lobes: the anterior, intermediate, and posterior lobes. In many animals, these lobes are distinct. However, in humans, the intermediate lobe is but a few cell layers thick and indistinct; as a result, it is often considered part of the anterior pituitary. In all animals, the fleshy, glandular anterior pituitary is distinct from theneural composition of thepars nervosa of theposterior pituitary.[citation needed]

The anterior pituitary is composed of three regions, the pars distalis, pars tuberalis, and pars intermedia.

Pars distalis

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The pars distalis (distal part) comprises the majority of the anterior pituitary and is where the bulk of pituitary hormone production occurs. The pars distalis contains two types of cells, includingchromophobe cells andchromophil cells.[1] The chromophils can be further divided intoacidophils (alpha cells) andbasophils (beta cells).[1] These cells all together produce hormones of the anterior pituitary and release them into the blood stream.[citation needed]

Nota bene: The terms "basophil" and "acidophil" are used by some books, whereas others prefer not to use these terms. This is due to the possible confusion with white blood cells, where one may also find basophils and acidophils.

  • Microanatomy of the pars distalis showing chromophobes, basophils, and acidophils
    Microanatomy of the pars distalis showing chromophobes, basophils, and acidophils
  • Eosinophilic follicles are a common normal finding in the anterior pituitary.
    Eosinophilic follicles are a common normal finding in the anterior pituitary.

Pars tuberalis

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The pars tuberalis (tubular part) forms a part of a highly vascularised sheath extending up from the pars distalis, which joins with thepituitary stalk (also known as the infundibular stalk orinfundibulum), arising from the posterior lobe. (The pituitary stalk connects the hypothalamus to the posterior pituitary.) The function of the pars tuberalis is poorly understood. However, it has been seen to be important in receiving the endocrine signal in the form ofTSHB (a β subunit of TSH), informing the pars tuberalis of thephotoperiod (length of day). The expression of this subunit is regulated by the secretion ofmelatonin in response to light information transmitted to thepineal gland.[2][3] Earlier studies have shown localization of melatonin receptors in this region.[4]

Principal cells of the pars tuberalis are low columnar in form, with the cytoplasm containing numerous lipid droplets, glycogen granules, and occasional colloid droplets. A sparse population of functional gonadotrophs are present (indicated by immunoreactivity forACTH,FSH, andLH).[5]

Pars intermedia

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Thepars intermedia (intermediate part) sits between the pars distalis and the posterior pituitary, forming the boundary between the anterior and posterior pituitaries. It is very small and indistinct in humans.

Development

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The anterior pituitary is derived from theectoderm, more specifically from that ofRathke's pouch, part of the developinghard palate in the embryo. Rathke's pouch is alsoectodermal in origin.

The pouch eventually loses its connection with thepharynx, giving rise to the anterior pituitary. The anterior wall of Rathke's pouch proliferates, filling most of the pouch to form the pars distalis and the pars tuberalis. The posterior wall of the anterior pituitary forms the pars intermedia. Its formation from the soft tissues of the upper palate contrasts with the posterior pituitary, which originates fromneuroectoderm.[6]

Function

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The anterior pituitary contains five types of endocrine cell, and they are defined by the hormones they secrete:somatotropes (GH);lactotropes (PRL);gonadotropes (LH and FSH);corticotropes (ACTH) andthyrotropes (TSH).[7] It also contains non-endocrinefolliculostellate cells which are thought to stimulate and support the endocrine cell populations.

Hormones secreted by the anterior pituitary aretrophic hormones (Greek: trophe, "nourishment"). Trophic hormones directly affect growth either as hyperplasia or hypertrophy on the tissue it is stimulating.Tropic hormones are named for their ability to act directly on target tissues or otherendocrine glands to release hormones, causing numerous cascading physiological responses.[6]

HormoneOther namesSymbol(s)StructureSecretory cellsStainingTargetEffect
Adrenocorticotropic hormoneCorticotropinACTHPolypeptideCorticotrophsBasophilAdrenal glandSecretion ofglucocorticoid,mineralocorticoid andandrogens
Thyroid-stimulating hormoneThyrotropinTSHGlycoproteinThyrotrophsBasophilThyroid glandSecretion ofthyroid hormones
Follicle-stimulating hormone-FSHGlycoproteinGonadotrophsBasophilGonadsGrowth ofreproductive system
Luteinizing hormoneLutropinLH, ICSHGlycoproteinGonadotrophsBasophilGonadsSex hormone production
Growth hormoneSomatotropinGH, STHPolypeptideSomatotrophsAcidophilLiver,adipose tissuePromotes growth;lipid andcarbohydrate metabolism
ProlactinLactotropinPRLPolypeptideLactotrophsAcidophilOvaries,mammary glands,testes,prostateSecretion ofestrogens/progesterone;lactation;spermatogenesis;prostatic hyperplasiaTSH andACTH secretion

[8][9]

Role in the endocrine system

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Main article:Hypothalamus

Hypothalamic control

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Hormone secretion from the anterior pituitary gland is regulated by hormones secreted by thehypothalamus.Neuroendocrine cells in the hypothalamus projectaxons to themedian eminence, at the base of the brain. At this site, these cells can release substances into small blood vessels that travel directly to the anterior pituitary gland (thehypothalamo-hypophyseal portal vessels).

Other mechanisms

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Aside from hypothalamic control of the anterior pituitary, other systems in the body have been shown to regulate the anterior pituitary's function.GABA can either stimulate or inhibit the secretion ofluteinizing hormone (LH) andgrowth hormone (GH) and can stimulate the secretion ofthyroid-stimulating hormone (TSH).Prostaglandins are now known to inhibitadrenocorticotropic hormone (ACTH) and also to stimulate TSH, GH and LH release.[10] Clinical evidence supports the experimental findings of the excitatory and inhibitory effects GABA has onGH secretion, dependent on GABA's site of action within the hypothalamic-pituitary axis.[11]

Effects of the anterior pituitary

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Thermal homeostasis

The homeostatic maintenance of the anterior pituitary is crucial to our physiological well being. Increased plasma levels ofTSH inducehyperthermia through a mechanism involving increasedmetabolism andcutaneousvasodilation. Increased levels ofLH also result inhypothermia but through a decreased metabolism action.ACTH increase metabolism and induce cutaneousvasoconstriction, increased plasma levels also result inhyperthermia andprolactin decreases with decreasing temperature values.Follicle-stimulating hormone (FSH) also may causehypothermia if increased beyond homeostatic levels through an increased metabolic mechanism only.[12]

Gonadal function

Gonadotropes, primarilyluteinising hormone (LH) secreted from the anterior pituitary stimulates theovulation cycle in femalemammals, whilst in the males, LH stimulates the synthesis ofandrogen which drives the ongoing will to mate together with a constant production ofsperm.[6]

HPA axis

Main articleHypothalamic-pituitary-adrenal axis

The anterior pituitary plays a role in stress response.Corticotropin releasing hormone (CRH) from the hypothalamus stimulatesACTH release in a cascading effect that ends with the production of glucocorticoids from theadrenal cortex.[6]

Behavioral effects

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Development
The release of GH, LH, and FSH are required for correct human development, including gonadal development.[13]
Breast-feeding
Release of the hormoneprolactin is essential forlactation.[13]
Stress
Operating through thehypothalamic-pituitary-adrenal axis (HPA), the anterior pituitary gland has a large role in theneuroendocrine system's stress response. Stress induces a release ofcorticotropin-releasing hormone (CRH) andvasopressin from thehypothalamus, which activates the release ofadrenocorticotropic hormone (ACTH) from the anterior pituitary gland. Then, this acts on theadrenal cortex to produceglucocorticoids such ascortisol. Theseglucocorticoids act back on the anterior pituitary gland and thehypothalamus withnegative feedback to slow the production of CRH and ACTH.[14][15] Increasedcortisol under stress conditions can cause the following: metabolic effects (mobilization ofglucose, fatty acids, andamino acids), bone re-absorption (calcium mobilization), activation of thesympathetic nervous system response (fight or flight), anti-inflammatory effects, and inhibition of reproduction/growth.[13] When the anterior pituitary gland is removed (hypophysectomy) in rats, theiravoidance learning mechanisms were slowed, but injections of ACTH restored their performance.[13] In addition, stress may delay the release of reproductive hormones such asluteinizing hormone (LH) andfollicle-stimulating hormone (FSH).[16] This shows that the anterior pituitary gland is involved in behavioral functions as well as being part of a larger pathway for stress responses. It is also known that (HPA) hormones are related to certain skin diseases and skin homeostasis. There is evidence linking hyperactivity of HPA hormones to stress-related skin diseases and skin tumors.[17]
Aging
Operating through thehypothalamic-pituitary-gonadal axis, the anterior pituitary gland also affects thereproductive system. The hypothalamus releasesgonadotropin-releasing hormone (GnRH), which stimulates the release ofluteinizing hormone (LH) andfollicle-stimulating hormone. Then thegonads produceestrogen andtestosterone. The decrease in release ofgonadotropins (LH and FSH) caused by normal aging may be responsible forimpotence[13][16] andfrailty[18] in elderly men because of the eventual decrease in production of testosterone. This lower level oftestosterone can have other effects, such as reducedlibido, well-being and mood, muscle and bone strength, and metabolism.[16]
Tactile responding
It has been shown that infant mice who were stroked with a paintbrush (simulating motherly care) had more release and binding ofgrowth hormone (GH) from the anterior pituitary gland.[13]
Circadian rhythms
Light information received by the eyes is transmitted to thepineal gland via thecircadian pacemaker (thesuprachiasmatic nucleus). Diminishing light stimulates the release ofmelatonin from the pineal gland which can also affect the secretion levels in thehypothalamic-pituitary-gonadal axis.[13] Melatonin can lower levels of LH and FSH, which will decrease levels ofestrogen and testosterone. In addition, melatonin may affect production ofprolactin.[19]

Clinical significance

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Increased activity

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Main article:Hyperpituitarism

Hyperpituitarism is the condition where the pituitary secretes excessive amounts of hormones. This hypersecretion often results in the formation of apituitary adenoma (tumour), which are benign apart from a tiny fraction. There are mainly three types of anterior pituitary tumors and their associated disorders. For example,acromegaly results from excessive secretion of growth hormone (GH) often being released by a pituitary adenoma. This disorder can cause disfigurement and possibly death[20] and can lead togigantism, a hormone disorder shown in "giants" such asAndré the Giant, where it occurs before theepiphyseal plates in bones close in puberty.[13] The most common type of pituitary tumour is aprolactinoma which hypersecretesprolactin.[21] A third type of pituitary adenoma secretes excess ACTH, which in turn, causes an excess ofcortisol to be secreted and is the cause ofCushing's disease.[13]

Decreased activity

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Main article:Hypopituitarism

Hypopituitarism is characterized by a decreased secretion of hormones released by the anterior pituitary. For example, hypo-secretion of GH prior to puberty can be a cause ofdwarfism. In addition,secondary adrenal insufficiency can be caused by hypo-secretion of ACTH which, in turn, does not signal the adrenal cortex to produce a sufficient amount ofcortisol. This is a life-threatening condition.Hypopituitarism could be caused by the destruction or removal of the anterior pituitary tissue through traumatic brain injury, tumor,tuberculosis, orsyphilis, among other causes. This disorder used to be referred to asSimmonds' disease but now according to theDiseases Database it is calledSheehan syndrome.[22] If the hypopituitarism is caused by the blood loss associated with childbirth, the disorder is referred to as Sheehan syndrome.

History

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Etymology

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The anterior pituitary is also known as theadenohypophysis, meaning "glandular undergrowth", from theGreekadeno- ("gland"),hypo ("under"), andphysis ("growth").

Additional images

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See also

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This article usesanatomical terminology.

References

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  1. ^abEroschenko, Victor P.; Fiore, Mariano S. H. di (2013-01-01).DiFiore's Atlas of Histology with Functional Correlations. Lippincott Williams & Wilkins.ISBN 978-1-4511-1341-9.
  2. ^Ikegami, K; Iigo, M; Yoshimura, T (2013)."Circadian clock gene Per2 is not necessary for the photoperiodic response in mice".PLOS ONE.8 (3) e58482.Bibcode:2013PLoSO...858482I.doi:10.1371/journal.pone.0058482.PMC 3591342.PMID 23505514.
  3. ^Dardente, H (2012). "Melatonin-dependent timing of seasonal reproduction by the pars tuberalis: pivotal roles for long daylengths and thyroid hormones".Journal of Neuroendocrinology.24 (2):249–66.doi:10.1111/j.1365-2826.2011.02250.x.PMID 22070540.S2CID 12723490.
  4. ^Morgan, PJ; Williams, LM (1996). "The pars tuberalis of the pituitary: a gateway for neuroendocrine output".Reviews of Reproduction.1 (3):153–61.doi:10.1530/ror.0.0010153.PMID 9414453.
  5. ^Ross, Michael. Histology: A Text and Atlas. 5th ed., 2006. pp 695
  6. ^abcdNelson, R. J. (2011) An Introduction to Behavioral Endocrinology, 4th Edition. Sunderland, MA: Sinauer Associates, Inc.ISBN 978-0878936205
  7. ^Le Tissier, P.R; Hodson, D.J; Lafont C; Fontanaud P; Schaeffer, M; Mollard, P. (2012) Anterior pituitary cell networks. Front Neuroendocrinol. Aug; 33(3):252-66
  8. ^Malendowicz, L.K; Rucinski, M; Belloni, A.S; Ziolkowska, A; and Nussdorfer, G.C. (2007) Leptin and the regulation of the hypothalamic-pituitary-adrenal axis. Int Rev Cytol. 263: 63-102.
  9. ^Sone, M. and Osamura, R.Y. (2001) Leptin and the pituitary. Pituitary. Jan-Apr; 4(1-2): 15-23.
  10. ^Hedge, G.A. (1977) Roles for the prostaglandins in the regulation of anterior pituitary secretion. Life Sci. Jan 1;20(1):17-33.
  11. ^Racagni, G; Apud, J.A; Cocchi, D; Locatelli, V; Muller, E.E. (1982) GABAergic control of anterior pituitary hormone secretion. Life Sci. Aug 30;31(9):823-38.
  12. ^Lin, M.T; Ho, L.T; and Uang, W.N. (1983) Effects of anterior pituitary hormones and their releasing hormones physiological and behavioral functions in rats. J. steroid Biochem. Vol. 19(1) 433-38.
  13. ^abcdefghiNelson, Randy J. (2011).An introduction to behavioral endocrinology (4th ed.). Sunderland, Massachusetts: Sinauer Associates.ISBN 978-0-87893-620-5.
  14. ^Aguilera, Greti (1998-10-01). "Corticotropin Releasing Hormone, Receptor Regulation and the Stress Response".Trends in Endocrinology & Metabolism.9 (8):329–336.doi:10.1016/S1043-2760(98)00079-4.ISSN 1043-2760.PMID 18406298.S2CID 30175791.
  15. ^Aguilera, Greti (December 1994). "Regulation of Pituitary ACTH Secretion during Chronic Stress".Frontiers in Neuroendocrinology.15 (4):321–350.doi:10.1006/frne.1994.1013.ISSN 0091-3022.PMID 7895891.S2CID 24818312.
  16. ^abcDobson, H; R F Smith (2000-07-02). "What is stress, and how does it affect reproduction?".Animal Reproduction Science.60–61:743–752.doi:10.1016/s0378-4320(00)00080-4.ISSN 0378-4320.PMID 10844239.
  17. ^Jung Eun Kim; Baik Kee Cho; Dae Ho Cho; Hyun Jeong Park (2013)."Expression of Hypothalamic-Pituitary-Adrenal Axis in Common Skin Diseases: Evidence of its Association with Stress-related Disease Activity". National Research Foundation of Korea. Retrieved4 March 2014.
  18. ^Tajar, Abdelouahid; O'Connell, Matthew D L; Mitnitski, Arnold B; O'Neill, Terence W; Searle, Samuel D; Huhtaniemi, Ilpo T; Finn, Joseph D; Bartfai, György; Boonen, Steven; Casanueva, Felipe F; Forti, Gianni; Giwercman, Aleksander; Han, Thang S; Kula, Krzysztof; Labrie, Fernand; Lean, Michael E J; Pendleton, Neil; Punab, Margus; Silman, Alan J; Vanderschueren, Dirk; Rockwood, Kenneth; Wu, Frederick C W; European Male Aging Study Group (May 2011). "Frailty in relation to variations in hormone levels of the hypothalamic-pituitary-testicular axis in older men: results from the European male aging study".Journal of the American Geriatrics Society.59 (5):814–821.doi:10.1111/j.1532-5415.2011.03398.x.hdl:20.500.11940/5770.ISSN 1532-5415.PMID 21568952.S2CID 43285151.
  19. ^Juszczak, Marlena; Monika Michalska (2006). "[The effect of melatonin on prolactin, luteinizing hormone (LH), and follicle-stimulating hormone (FSH) synthesis and secretion]".Postępy Higieny I Medycyny Doświadczalnej.60:431–438.ISSN 1732-2693.
  20. ^Scacchi, Massimo; Francesco Cavagnini (2006). "Acromegaly".Pituitary.9 (4):297–303.doi:10.1007/s11102-006-0409-4.ISSN 1573-7403.PMID 17077948.
  21. ^Ciccarelli, E; F Camanni (June 1996). "Diagnosis and drug therapy of prolactinoma".Drugs.51 (6):954–965.doi:10.2165/00003495-199651060-00004.ISSN 0012-6667.PMID 8736617.S2CID 35481175.
  22. ^Summers, V. K. (September 1947)."Diagnosis and Treatment of Simmonds' Disease".Postgraduate Medical Journal.23 (263):441–443.doi:10.1136/pgmj.23.263.441.ISSN 0032-5473.PMC 2529616.PMID 20258051.

Further reading

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  • Marieb, E. 2004. Human Anatomy and Physiology. Benjamin Cummings: New York.
  • Wheater, P., Burkitt, H., Daniels, V. 1987. Functional Histology. Churchill Livingstone: New York.

External links

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Anatomy of theendocrine system
Pituitary gland
Anterior
Posterior
Thyroid
Parathyroid gland
Adrenal gland
Cortex
Medulla
Gonads
Islets of pancreas
Pineal gland
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