Pituitary gland

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The pituitary gland, or hypophysis, is a pea-sized gland of the endocrine system, situated at the base of the brain. As part of the HPA axis, it is regulated by the hypothalamus to produce, store, and secrete various hormones, which target other endocrine glands. The pituitary gland is sometimes referred to as the “master gland” as it regulates the function of the other endocrine glands.[1]

Structure and Function[edit | edit source]

Anatomical diagram of the pituitary gland, depicting the posterior, anterior, and intermediate lobes.[2]

The pituitary gland sits at the base of the brain, underneath the hypothalamus. It is surrounded by a protective bony cavity called the sella turcica. The pituitary is divided into three distinct lobes: posterior, anterior, and intermediate.[3]

Posterior[edit | edit source]

The posterior pituitary develops as an extension of the hypothalamus (distinct from the anterior pituitary). The posterior pituitary is largely made up of the terminals of nerve cells of the hypothalamus, as neurons in the hypothalamus project directly to the posterior pituitary. Hormones produced by the hypothalamus are stored in the terminals of hypothalamic neurons in the posterior pituitary, and are released by nerve excitation. The two major hormones stored and secreted by the posterior pituitary include:

Anterior[edit | edit source]

The anterior pituitary is structurally distinct from the posterior pituitary. It makes up 80% of the pituitary gland, and is made up of different types of endocrine cells. These cells are classified by the hormones they synthesize and release, and are regulated by the hypothalamus via releasing and inhibiting hormones. The six major hormones of the anterior pituitary are:

Intermediate[edit | edit source]

The intermediate lobe is present in many lower vertebrates, but is almost absent in humans. The intermediate pituitary synthesizes and secretes:

Function of Pituitary Hormones[edit | edit source]

Hormone Target Organ Role
Growth hormone (GH) Muscular, skeletal, and fat tissue Regulates growth and physical development by stimulating muscle growth and reducing fat tissue
Adrenocorticotropic hormone (ACTH) Adrenal glands Stimulates the adrenal glands to produce cortisol and other hormones
Thyroid-stimulating hormone (TSH) Thyroid gland Stimulates the thyroid to produce thyroid hormone
Follicular-stimulating hormone (FSH) Ovaries or testes Stimulates the ovaries to produce eggs/the testes to produce sperm, and the sex organs to produce sex hormones
Luteinizing hormone (LH) Ovaries or testes Stimulates the ovaries to produce eggs/the testes to produce sperm, and the sex organs to produce sex hormones
Prolactin Mammary glands Stimulates the mammary glands to produce milk
Antidiuretic hormone (ADH, also known as vasopressin) Kidneys Regulates amount of water absorbed and excreted by the kidneys
Oxytocin Uterus and mammary glands Causes uterus contraction during childbirth, stimulates contractions of the milk ducts in breast for breastfeeding
Melanocyte-stimulating hormone (MSH) Skin and hair Stimulates the production of melanin in skin and hair, suppresses appetite, contributes to sexual arousal

[7]

Diagram of the pituitary gland, the hormones it releases, and its target organs.[8]

Dysfunction and Disease[edit | edit source]

Dysfunction of the pituitary gland can result in overproduction or underproduction of pituitary hormones, thus having major consequences in bodily function. Conditions of pituitary malfunction include:

ME[edit | edit source]

Dysfunction of the endocrine system, with a focus on HPA axis hypofunction, has been reported in individuals with ME.[10][11][12][13]. It has been suggested that HPA axis hypofunction in ME is caused by chronic activation of the inflammatory and oxidative and nitrosative stress pathways[13]. However, this area of research continues to lack studies with direct measures of pituitary function.

Some patients report that there seems to be a period of pituitary/HPA axis hyperfunction in the earlier stage of ME, whereas later in disease progression there's a switch to hypofunction. This could perhaps explain some of the wide variation across studies (e.g.,[14][15][16]).

Patients with ME have also reported other problems with the pituitary, such as Empty Sella Syndrome and pituitary adenoma. These may be of note to guide future research.

Learn more[edit | edit source]

Khan Academy | The hypothalamus and pituitary gland

References[edit | edit source]

  1. "Overview of the Pituitary Gland - Hormonal and Metabolic Disorders - Merck Manuals Consumer Version". Merck Manuals Consumer Version. Retrieved Oct 25, 2018. 
  2. Darling, David. "pituitary gland". www.daviddarling.info. Retrieved Oct 25, 2018. 
  3. "Overview of the Pituitary Gland - Hormonal and Metabolic Disorders - Merck Manuals Consumer Version". Merck Manuals Consumer Version. Retrieved Oct 25, 2018. 
  4. Nussey, Stephen; Whitehead, Saffron (2001). The pituitary gland. BIOS Scientific Publishers. 
  5. Nussey, Stephen; Whitehead, Saffron (2001). The pituitary gland. BIOS Scientific Publishers. 
  6. "Overview of the Pituitary Gland - Hormonal and Metabolic Disorders - Merck Manuals Consumer Version". Merck Manuals Consumer Version. Retrieved Oct 25, 2018. 
  7. "Overview of the Pituitary Gland - Hormonal and Metabolic Disorders - Merck Manuals Consumer Version". Merck Manuals Consumer Version. Retrieved Oct 25, 2018. 
  8. "Pituitary Gland – Control And Hormones of Anterior And Posterior Lobe". www.earthslab.com. Retrieved Oct 25, 2018. 
  9. "Pituitary disease". Wikipedia. Aug 11, 2018. 
  10. Nijhof, Sanne L.; Rutten, Juliette M. T. M.; Uiterwaal, Cuno S. P. M.; Bleijenberg, Gijs; Kimpen, Jan L. L.; Putte, Elise M. van de (Apr 2014). "The role of hypocortisolism in chronic fatigue syndrome". Psychoneuroendocrinology. 42: 199–206. doi:10.1016/j.psyneuen.2014.01.017. ISSN 1873-3360. PMID 24636516. 
  11. Papadopoulos, Andrew S.; Cleare, Anthony J. (Sep 27, 2011). "Hypothalamic-pituitary-adrenal axis dysfunction in chronic fatigue syndrome". Nature Reviews. Endocrinology. 8 (1): 22–32. doi:10.1038/nrendo.2011.153. ISSN 1759-5037. PMID 21946893. 
  12. Heim, Christine; Nater, Urs M.; Maloney, Elizabeth; Boneva, Roumiana; Jones, James F.; Reeves, William C. (Jan 2009). "Childhood trauma and risk for chronic fatigue syndrome: association with neuroendocrine dysfunction". Archives of General Psychiatry. 66 (1): 72–80. doi:10.1001/archgenpsychiatry.2008.508. ISSN 1538-3636. PMID 19124690. 
  13. 13.013.1 Morris, Gerwyn; Anderson, George; Maes, Michael (Oct 20, 2016). "Hypothalamic-Pituitary-Adrenal Hypofunction in Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS) as a Consequence of Activated Immune-Inflammatory and Oxidative and Nitrosative Pathways". Molecular Neurobiology. 54 (9): 6806–6819. doi:10.1007/s12035-016-0170-2. ISSN 0893-7648. 
  14. DEMITRACK, MARK A.; DALE, JANET K.; STRAUS, STEPHEN E.; LAUE, LOUISA; LISTWAK, SAM J.; KRUESI, MARKUS J. P.; CHROUSOS, GEORGE P.; GOLD, PHILIP W. (Dec 1991). "Evidence for Impaired Activation of the Hypothalamic-Pituitary-Adrenal Axis in Patients with Chronic Fatigue Syndrome". The Journal of Clinical Endocrinology & Metabolism. 73 (6): 1224–1234. doi:10.1210/jcem-73-6-1224. ISSN 0021-972X. 
  15. Di Giorgio, Annabella; Hudson, Marina; Jerjes, Walid; Cleare, Anthony J. (May 2005). "24-hour pituitary and adrenal hormone profiles in chronic fatigue syndrome". Psychosomatic Medicine. 67 (3): 433–440. doi:10.1097/01.psy.0000161206.55324.8a. ISSN 1534-7796. PMID 15911907. 
  16. "Basal circadian and pulsatile ACTH and cortisol secretion in patients with fibromyalgia and/or chronic fatigue syndrome". Brain, Behavior, and Immunity. 18 (4): 314–325. Jul 1, 2004. doi:10.1016/j.bbi.2003.12.011. ISSN 0889-1591. 

Myalgic encephalomyelitis or M.E. has different diagnostic criteria to chronic fatigue syndrome; neurological symptoms are required but fatigue is an optional symptom.<ref name="ICP2011primer">{{Citation


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From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history