Adrenal gland

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Adrenal Gland
Illu endocrine system New.png
Illu adrenal gland.jpg
Adrenal gland
Details
Latin Glandula suprarenalis
System Endocrine system
Superior, middle and inferior suprarenal arteries
Suprarenal veins
Celiac and renal plexus
Lumbar lymph nodes
Precursor Mesoderm and neural crest
Identifiers
Gray's p.1278
MeSH A06.407.071
Dorlands
/Elsevier
Adrenal gland
TA A11.5.00.001
FMA 9604
Anatomical terminology

In mammals, the adrenal glands (also known as suprarenal glands) are endocrine glands that are located on the top of the kidneys. They are chiefly responsible for releasing hormones in response to stress through the synthesis of corticosteroids such as cortisol and catecholamines such as adrenaline (epinephrine) and noradrenaline. They also produce androgens in their innermost cortical layer. The adrenal glands affect kidney function through the secretion of aldosterone, and recent data (1998) suggest that adrenocortical cells under pathological as well as under physiological conditions show neuroendocrine properties; within normal adrenal glands, this neuroendocrine differentiation seems to be restricted to cells of the zona glomerulosa and might be important for an autocrine regulation of adrenocortical function.[1]

Structure[edit]

The adrenal glands are located bilaterally in the retroperitoneum superior and slightly medial to the kidneys.

Histology section of human adrenal gland, showing the different layers that compose it. From the surface to the center: zona glomerulosa, zona fasciculata, zona reticularis, medulla. In the medulla, the central adrenomedullary vein is visible.

In humans, the right adrenal gland is triangular in shape, whereas the left adrenal gland is semilunar in shape;[2] in non-humans, they are quadrilateral in shape. The combined weight of the adrenal glands in an adult human ranges from 7 to 10 grams.[3] They are surrounded by an adipose capsule and renal fascia.

Each adrenal gland has two distinct structures, the outer adrenal cortex and the inner medulla, both of which produce hormones. The cortex mainly produces cortisol, aldosterone and androgens, while the medulla chiefly produces adrenaline and noradrenaline. In contrast to the direct innervation of the medulla, the cortex is regulated by neuroendocrine hormones secreted from the pituitary gland which are under the control of the hypothalamus, as well as by the renin-angiotensin system.

Cortex[edit]

Main article: Adrenal cortex

The adrenal cortex is devoted to production of corticosteroid and androgen hormones. Specific cortical cells produce particular hormones including aldosterone, cortisol, and androgens such as androstenedione. Under normal unstressed conditions, the human adrenal glands produce the equivalent of 35–40 mg of cortisone acetate per day.[4]

The adrenal cortex comprises three zones, or layers. This anatomic zonation can be appreciated at the microscopic level, where each zone can be recognized and distinguished from one another based on structural and anatomic characteristics.[5] The adrenal cortex exhibits functional zonation as well: by virtue of the characteristic enzymes present in each zone, the zones produce and secrete distinct hormones.[5]

Zona glomerulosa[edit]

Sections of human adrenal glands immunostained for neuronal cell adhesion molecule (NCAM). Staining for NCAM was restricted to the zona glomerulosa (zg) and the adrenal medulla (m).[1]

The outermost layer, the zona glomerulosa is the main site for production of aldosterone, a mineralocorticoid, by the action of the enzyme aldosterone synthase (also known as CYP11B2).[6][7] Aldosterone is largely responsible for the long-term regulation of blood pressure.[8]

The expression of neuron-specific proteins in the zona glomerulosa cells of human adrenocortical tissues has been predicted and reported by several authors[1][9][10] and it was suggested that the expression of proteins like the neuronal cell adhesion molecule (NCAM) in the cells of the zona glomerulosa reflects the regenerative feature of these cells, which would lose NCAM immunoreactivity after moving to the zona fasciculata.[1][11] However, together with other data on neuroendocrine properties of zona glomerulosa cells, NCAM expression may reflect a neuroendocrine differentiation of these cells.[1] Voltage-dependent calcium channels have been detected in the zona glomerulosa of the human adrenal, which suggests that calcium-channel blockers may directly influence the adrenocortical biosynthesis of aldosterone in vivo.[12]

Zona fasciculata[edit]

Situated between the glomerulosa and reticularis, the zona fasciculata is responsible for producing glucocorticoids, such as 11-deoxycorticosterone, corticosterone, and cortisol in humans.[13]

Zona reticularis[edit]

The inner most cortical layer, the zona reticularis produces androgens, mainly dehydroepiandrosterone (DHEA), DHEA sulfate (DHEA-S), and androstenedione (the precursor to testosterone) in humans.[13]

Medulla[edit]

Main article: Adrenal medulla

The adrenal medulla is the core of the adrenal gland, and is surrounded by the adrenal cortex. It secretes approximately 20% noradrenaline (norepinephrine) and 80% adrenaline (epinephrine).[13] The chromaffin cells of the medulla, named for their characteristic brown staining with chromic acid salts, are the body's main source of the circulating catecholamines adrenaline and noradrenaline. Catecholamines are derived from the amino acid tyrosine and these water-soluble hormones are the major hormones underlying the fight-or-flight response.

To carry out its part of this response, the adrenal medulla receives input from the sympathetic nervous system through preganglionic fibers originating in the thoracic spinal cord from T5–T11.[14] Because it is innervated by preganglionic nerve fibers, the adrenal medulla can be considered as a specialized sympathetic ganglion.[14] Unlike other sympathetic ganglia, however, the adrenal medulla lacks distinct synapses and releases its secretions directly into the blood.

Cortisol also promotes adrenaline synthesis in the medulla. Produced in the cortex, cortisol reaches the adrenal medulla and at high levels, the hormone can promote the upregulation of phenylethanolamine N-methyltransferase (PNMT), thereby increasing adrenaline synthesis and secretion.[5]

Blood supply[edit]

Although variations of the blood supply to the adrenal glands (and indeed the kidneys themselves) are common, there are usually three arteries that supply each adrenal gland:

Venous drainage of the adrenal glands is achieved via the suprarenal veins:

In the medulla a particular type of blood vessel called central adrenomedullary vein exists. Its structure is different from the other veins in that the smooth muscle in its tunica media (the middle layer of the vessel) is arranged in conspicuous, longitudinally oriented bundles.[15]

The suprarenal vein exits the adrenal gland through a depression on its anterior surface known as the hilum. Note that the arteries supplying the suprarenal gland do not pass through the hilum.[16] The suprarenal veins may form anastomoses with the inferior phrenic veins. Since the right supra-renal vein is short and drains directly into the inferior vena cava it is likely to injure the latter during removal of right adrenal for various reasons.

The adrenal glands (alongside the thyroid gland) have one of the greatest blood supply per gram of tissue of any organ. Up to 60 arterioles may enter each adrenal gland.[17] This may be one of the reasons lung cancer commonly metastasizes to the adrenals.

Function[edit]

The adrenal gland secretes a number of different hormones which are metabolised by enzymes either within the gland or in other parts of the body. These hormones are involved in a number of different pathways.[18]

Aldosterone and mineralocorticoids[edit]

Aldosterone's effects are on the distal convoluted tubule and collecting duct of the kidney where it causes increased reabsorption of sodium and increased excretion of both potassium (by principal cells) and hydrogen ions (by intercalated cells of the collecting duct).[8] Sodium retention is also a response of the distal colon, and sweat glands to aldosterone receptor stimulation. Although sustained production of aldosterone requires persistent calcium entry through low-voltage activated Ca2+ channels, isolated zona glomerulosa cells are considered nonexcitable, with recorded membrane voltages that are too hyperpolarized to permit Ca2+ channels entry.[19] However, mouse zona glomerulosa cells within adrenal slices spontaneously generate membrane potential oscillations of low periodicity; this innate electrical excitability of zona glomerulosa cells provides a platform for the production of a recurrent Ca2+ channels signal that can be controlled by angiotensin II and extracellular potassium, the 2 major regulators of aldosterone production.[19] Angiotensin II originates from plasmatic angiotensin I after the conversion of angiotensinogen by renin produced by the juxtaglomerular cells of the kidney.[13]

Cortisol and glucocorticoids[edit]

Cortisol is the main glucocorticoid under normal conditions and its actions include mobilization of fats, proteins, and carbohydrates, but it does not increase under starvation conditions.[13] Additionally, cortisol enhances the activity of other hormones including glucagon and catecholamines. The zona fasciculata secretes a basal level of cortisol but can also produce bursts of the hormone in response to adrenocorticotropic hormone (ACTH) from the anterior pituitary.

Androgen production[edit]

Cells in zona reticularis of the adrenal glands produce male sex hormones, or androgens, the most important of which is DHEA. In general, these hormones do not have an overall effect in the male body, and are converted to more potent androgens such as testosterone and DHT or to estrogens (female sex hormones) in the gonads, acting in this way as a metabolic intermediate.[20]

Synthesis of DHEA in the adrenal gland starts with pregnenolone, a common precursor to all steroid hormones that is produced from cholesterol. An intermediate step is required to generate DHEA, in which pregnenolone is converted to 17-hydroxypregnenolone by the enzyme 17α-hydroxylase. The same enzyme then catalizes the conversion of the previous metabolite into DHEA. A mutation that impairs the ability of the enzyme to catalize the reaction leads to an uncommon form of congenital adrenal hyperplasia.[21]

Adrenaline and noradrenaline[edit]

The adrenal glands are responsible for the majority of circulating adrenaline in the body, but only a small amount of circulating noradrenaline.[18] These substances are released in the adrenal medulla, which is richly vascular. Under the influence of cortisol, the medulla releases adrenaline. The medulla can be considered an extension of the sympathetic nervous system which releases adrenaline into the blood stream rather than into a synapse as a neurotransmitter.[18] Adrenaline and noradrenaline are catecholamines that act at adrenoreceptors throughout the body, with effects including constriction of small arteries, dilation of veins, and increasing the heart rate.[18]

Development[edit]

The adrenal glands are composed of two very heterogenous types of tissue: in the center there is the adrenal medulla, which produces and releases mostly adrenaline to the blood in stress situations as part of the sympathetic nervous system. Surrounding the medulla is the cortex, which produces a wide variety of steroid hormones. These tissues come from different embryological precursors and have distinct prenatal developments.

Cortex[edit]

Adrenal cortex tissue is derived from the intermediate mesoderm, first appearing 33 days after fecundation, showing stereidogenic (steroid hormone production) capabilities by the eighth week and growing rapidly during the first trimester of pregnancy. The fetal adrenal cortex is different from its adult counterpart, as it is composed of two distinct zones: the inner fetal zone, which carries most of the hormone-producing activity, and the outer definitive zone, which is in a proliferative phase. The fetal zone produces large amounts of adrenal androgens (male sex hormones) that are used by the placenta for estrogen biosynthesis.[22] Cortical development of the adrenal gland is regulated mostly by ACTH, a hormone produced by the pituitary gland that stimulates cortisol synthesis.[23] During midgestation, the fetal zone occupies most of the cortical volume and produces 100–200 mg/day of DHEA-S, an androgen and precursor of both androgens and estrogens (female sex hormones).[24] Adrenal hormones, especially glucocorticoids such as cortisol are considered essential for prenatal development of organs, particularly for the maduration of the fetal lungs. The adrenal gland decreases in size after birth because of the rapid disappearance of the fetal zone, with a decrease in androgen secretion.[22]

Medulla[edit]

The adrenal medulla is derived from a type of cells known as neural crest cells, which come from the ectoderm layer of the embryo. These cells migrate from their initial position and aggregate in the vicinity of the dorsal aorta, a primitive blood vessel, which activates the differentiation of these cells through the release of proteins known as BMPs. These cells then undergo a second migration step away from the dorsal aorta to form the the adrenal medulla, along other organs of the sympathetic nervous system.[25] Cells of the adrenal medulla are also called chromaffin cells because they contain granules that stain with chromium salts, a characteristic not present in all sympathetic organs. Glucocorticoid production by the adrenal cortex was thought to be responsible for this differentiation, but now the available data suggest that BMP-4 secreted in the adrenal tissue is the primary responsible for the differentiation, and that glucocorticoids have a role in the posterior development of the cells.[26]

Clinical significance[edit]

History[edit]

Etymology[edit]

The adrenal glands are named for their location relative to the kidneys. The term "adrenal" comes from ad- (Latin, "near") and renes (Latin, "kidney").[27] Similarly, "suprarenal" is derived from supra- (Latin, "above") and renes.

See also[edit]

This article uses anatomical terminology; for an overview, see anatomical terminology.

References[edit]

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  2. ^ "FeedBack What Is Adrenal Gland? Adrenal Gland Diseases". OrgansOfTheBody. Retrieved 2013-09-17. 
  3. ^ Page 18 in: Boué A, Nicolas A, Montagnon B (June 1971). "Reinfection with rubella in pregnant women". Lancet 297 (7712): 1251–3. doi:10.1016/S0140-6736(71)91775-2. PMID 4104713. 
  4. ^ Jefferies, William McK (2004). Safe uses of cortisol. Springfield, Ill: Charles C. Thomas. ISBN 0-398-07500-X. 
  5. ^ a b c Whitehead, Saffron A.; Nussey, Stephen (2001). Endocrinology: an integrated approach. Oxford: BIOS. p. 122. ISBN 1-85996-252-1. 
  6. ^ Curnow KM, Tusie-Luna MT, Pascoe L, Natarajan R, Gu JL, Nadler JL, White PC (October 1991). "The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex.". Mol. Endocrinol. 5 (10): 1513–1522. doi:10.1210/mend-5-10-1513. PMID 1775135. 
  7. ^ Zhou M, Gomez-Sanchez CE (July 1993). "Cloning and expression of a rat cytochrome P-450 11 beta-hydroxylase/aldosterone synthase (CYP11B2) cDNA variant.". Biochem Biophys Res Commun. 194 (1): 112–117. doi:10.1006/bbrc.1993.1792. PMID 8333830. 
  8. ^ a b Marieb Human Anatomy & Physiology 9th edition, chapter:16, page:629, question number:14
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  13. ^ a b c d e Dunn R. B.; Kudrath W.; Passo S.S.; Wilson L.B. (2011). "10". Kaplan USMLE Step 1 Physiology Lecture Notes. pp. 263–289. 
  14. ^ a b Sapru, Hreday N.; Siegel, Allan (2007). Essential Neuroscience. Hagerstown, MD: Lippincott Williams & Wilkins. ISBN 0-7817-9121-9. 
  15. ^ Ross M, Pawlina W (2006). Histology: A Text and Atlas. 5th edition. Lippincot Williams & Wilkins. p. 708. ISBN 978-0781772211. 
  16. ^ http://medicine.academic.ru/130143/hilum_glandulae_suprarenalis
  17. ^ Mirilas P, Skandalakis JE, Colborn GL, Weidman TA, Foster RS, Kingsnorth A, Skandalakis LJ, Skandalakis PN (2004). Surgical Anatomy: The Embryologic And Anatomic Basis Of Modern Surgery. McGraw-Hill Professional Publishing. ISBN 960-399-074-4. 
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External links[edit]