Sweat glands (also known as sudoriferous or sudoriparous glands, from Latinsudor, meaning "sweat"), are small tubular structures of the skin that produce sweat. There are two main types of sweat glands:
Eccrine sweat glands are distributed almost all over the body, though their density varies from region to region. Humans utilize eccrine sweat glands as a primary form of cooling.
Domestic animals[which?] have apocrine glands at the base of each hair follicle but eccrine glands only in foot pads and snout. Their apocrine glands, like those in humans, produce an odorless oily milky secretion evolved not to evaporate and cool but rather coat and stick to hair so odor-causing bacteria can grow on it. Eccrine glands on their foot pads, like those on palms and soles of humans, did not evolve to cool either but rather increase friction and enhance grip.
Both apocrine and eccrine sweat glands contain myoepithelial cells (from Greek myo– "muscle"), specialized epithelial cells located between the gland cells and the underlying basal lamina. Myoepithelial cell contractions squeeze the gland and discharge the accumulated secretions. The secretory activities of the gland cells and the contractions of myoepithelial cells are controlled by both the autonomic nervous system and by the circulating hormones.
Sweat glands are simple tubules consisting of a base rolled into a glomerulum and a duct that carries the sweat away. The base, which forms the secretory coil, is set deep in the hypodermis, and the entire gland is surrounded by adipose tissue. In apocrine glands, the secretory tubule is branched and single-layered, whereas it is unbranched, coiled, and double-layered in eccrine glands. All sweat glands' secretory coils are wrapped in long, rod-like contractile myoepithelial cells. In apocrine and eccrine glands, the diameter of the overall coil is around 800 and 500–700 µm respectively. The tubules themselves are also wider in apocrine glands: they have an inner diameter of 80–100 µm, versus the 30–40 µm diameters in eccrine glands. Excretory ducts, which carry sweat away from the secretory coil, are lined by a double layer of cuboidal cells.
Each sweat gland receives several nerve fibers that branch out into bands of one or more axons and encircle the individual tubules of the secretory coil. Capillaries are also interwoven among sweat tubules.
The number of active sweat glands varies greatly among different people, though comparisons between different areas (ex. axillae versus groin) show the same directional changes (certain areas always have more active sweat glands while others always have fewer). According to Henry Gray's estimates, the palm has around 370 sweat glands per cm2; the back of the hand has 200 per cm2; the forehead has 175 per cm2; the breast, abdomen, and forearm have 155 per cm2; and the back and legs have 60–80 per cm2.
In the finger pads, sweat glands are somewhat irregularly spaced on the epidermal ridges. There are no pores between the ridges, though sweat tends to spill into them. The thick epidermis of the palms and soles causes the sweat glands to become spirally coiled.
Non-primate mammals have eccrine sweat glands only on the palms and soles. Apocrine glands cover the rest of the body, though they are not as effective as humans' in temperature regulation (with the exception of horses').Prosimians have a 1:20 ratio of follicles with apocrine glands versus follicles without. They have eccrine glands between hairs over most of their body (while humans have them between the hairs on their scalp. The overall distribution of sweat glands varies among primates: the rhesus and patas monkeys have them on the chest; the squirrel monkey has them only on the palms and soles; and the stump-tailed macaque, Japanese monkey, and baboon have them over the entire body.
Apocrine sweat glands are found in the armpit, areola (around the nipples), perineum (between the anus and genitals), in the ear, and in the eyelids. The secretory portion is larger than that of eccrine glands (making them larger overall). Rather than opening directly onto the surface of the skin, apocrine glands secrete sweat into the pilary canal of the hair follicle.
Before puberty, the apocrine sweat glands are inactive;hormonal changes in puberty cause the glands to increase in size and begin functioning. The substance secreted is thicker than eccrine sweat and provides nutrients for bacteria on the skin: the bacteria's decomposition of sweat is what creates the acrid odor. Apocrine sweat glands are most active in times of stress and sexual excitement.
In mammals (including humans), apocrine sweat contains pheromone-like compounds to attract the opposite sex. Study of human sweat has revealed differences between men and women in apocrine secretions and bacteria.
Eccrine sweat glands are everywhere except the lips, ear canal, prepuce, glans penis, labia minora, and clitoris. They are ten times smaller than apocrine sweat glands, do not extend as deeply into the dermis, and excrete directly onto the surface of the skin. The proportion of eccrine glands decreases with age.
The clear secretion produced by eccrine sweat glands is termed sweat or sensible perspiration. Sweat is mostly water, but it does contain some electrolytes, since it is derived from blood plasma. The presence of sodium chloride gives sweat a salty taste.
The total volume of sweat produced depends on the number of functional glands and the size of the surface opening. The degree of secretory activity is regulated by neural and hormonal mechanisms (men sweat more than women). When all of the eccrine sweat glands are working at maximum capacity, the rate of perspiration for a human being may exceed three liters per hour, and dangerous losses of fluids and electrolytes can occur.
Eccrine glands have three primary functions:
Thermoregulation: sweat cools the surface of the skin and reduces body temperature.
Excretion: eccrine sweat gland secretion can also provide a significant excretory route for water and electrolytes.
Protection: eccrine sweat gland secretion aids in preserving the skin's acid mantle, which helps protect the skin from colonization from bacteria and other pathogenic organisms.
Some human sweat glands cannot be classified as either apocrine or eccrine, having characteristics of both; such glands are termed apoeccrine. They are larger than eccrine glands, but smaller than apocrine ones; their secretory portion has a narrow portion similar to secretory coils in eccrine glands as well as a wide section reminiscent of apocrine glands.
Apoeccrine, found in the armpits and perianal region, have ducts opening onto the skin surface. They are presumed to have developed in puberty from the eccrine glands, and can comprise up to 50% of all axillary glands. Apoeccrine glands secrete more sweat than both eccrine and apocrine glands, thus playing a large role in axillary sweating. Apoeccrine glands are sensitive to cholinergic activity, though they can also be activated via adrenergic stimulation. Like eccrine glands, they continuously secrete a thin, watery sweat.
Sweat glands are used to regulate temperature and remove waste by secreting water, sodium salts, and nitrogenous waste (such as urea) onto the skin surface. The main electrolytes of sweat are sodium and chloride, though the amount is small enough to make sweat hypotonic at the skin surface. Eccrine sweat is clear, odorless, and is composed of 98–99% water; it also contains NaCl, fatty acids, lactic acid, citric acid, absorbic acid, urea, and uric acid. Its pH ranges from 4 to 6.8. On the other hand, the apocrine sweat has a pH of 6 to 7.5; it contains water, proteins, carbohydrate waste material, lipids, and steroids. The sweat is oily, cloudy, viscous, and originally odorless; it gains odor upon decomposition by bacteria. Because both apocrine glands and sebaceous glands open into the hair follicle, apocrine sweat is mixed with sebum.
In apocrine secretion (pictured), portions of the cell are pinched off and later disintegrate.
It was originally thought that both apocrine and eccrine sweat glands used merocrine secretion, where vesicles in the gland released sweat via exocytosis, leaving the entire cell intact. More recent studies have revealed that apocrine glands release sweat in the hair follicle via apocrine secretion, where portions of the cell are actually pinched off, and disintegrate later to excrete sweat.
In both apocrine and eccrine sweat glands, the sweat is originally produced in the gland's coil, where it is isotonic with the blood plasma there. When the rate of sweating is low, salt is conserved and reabsorbed by the gland's duct; high sweat rates, on the other hand, lead to less salt reabsorption and allow more water to evaporate on the skin (via osmosis) to increase evaporative cooling.
Secretion of sweat occurs when the myoepithelial cell cells surrounding the secretory glands contract. Eccrine sweat increases the rate of bacterial growth and volatilizes the odor compounds of apocrine sweat, strengthening the latter's acrid smell.
Normally, only a certain number of sweat glands are actively producing sweat. When stimuli call for more sweating, more sweat glands are activated, with each then producing more sweat.
Both eccrine and apocrine sweat glands participate in thermal (thermoregulatory) sweating, which is directly controlled by the hypothalamus. Thermal sweating is stimulated by a combination of internal body temperature and mean skin temperature. In eccrine sweat glands, stimulation occurs via activation by acetylcholine, which binds to the gland's muscarinic receptors.
Emotional sweating is stimulated by stress, anxiety, fear, and pain; it is independent of ambient temperature. Acetylcholine acts on the eccrine glands and adrenaline acts on both eccrine and apocrine glands to produce sweat. Emotional sweating can occur anywhere, though it is most evident on the palms, soles of the feet, and axillary regions. Sweating on the palms and soles is thought to have evolved as a fleeing reaction in mammals: it increases friction and prevents slipping when running or climbing in stressful situations.
Gustatory sweating refers to thermal sweating induced by the ingestion of food. The increase in metabolism caused by ingestion raises body temperature, leading to thermal sweating. Hot and spicy foods also leads to mild gustatory sweating in the face, scalp and neck: capsaicin (the compound that makes spicy food taste "hot"), binds to receptors in the mouth that detect warmth. The increased stimulation of such receptors induces a thermoregulatory response.
Unlike deodorant, which simply reduces axillary odor without affecting body functions, antiperspirant reduces both eccrine and apocrine sweating. Antiperspirants, which are classified as drugs, cause proteins to precipitate and mechanically block eccrine (and sometimes apocrine) sweat ducts. The metal salts found in antiperspirants alters the keratinfibrils in the ducts; the ducts then close and form a "horny plug". The main active ingredients in modern antiperspirants are aluminum chloride, aluminum chlorohydrate, aluminum zirconium chlorohydrate, and buffered aluminum sulfate.
Also known as hyperidrosis (without the h after hyper). Hyperhidrosis is a pathological, excessive sweating that can be either generalized or localized (focal hyperhidrosis); focal hyperhidrosis occurs most often on the palms, soles, face, scalp and axillae. Hyperhidrosis is usually brought on by emotional or thermal stress, but it can also occur or with little to no stimulus. Local (or asymmetrical) hyperhidrosis is said to be caused by problems in the sympathetic nervous system: either lesions or nerve inflammation. Hyperhidrosis can also be caused by trench foot or encephalitis.
Also called prickly heat. Milaria rubia is the rupture of sweat glands and migration of sweat to other tissues. In hot environments, the skin's horny layer can expand due to sweat retention, blocking the ducts of eccrine sweat glands. The glands, still stimulated by high temperatures, continues to secrete. Sweat builds up in the duct, causing enough pressure to rupture the duct where it meets the epidermis. Sweat also escapes the duct to adjacent tissues (a process called milaria). Hypohydrosis then follows milaria (postmiliarial hypohydrosis).
Often called bromhidrosis, especially in combination with hyperhidrosis. Osmohidrosis is excessive odor from apocrine sweat glands (which are overactive in the axillae). Osmidrosis is thought to be caused by changes in the apocrine gland structure rather than changes in the bacteria that acts on sweat.
Lafora disease is a rare genetic disorder marked by the presence of abnormal polyglucosan deposits. These "Lafora bodies" appear in the ducts of sweat glands, as well as the myoepithelial cells of apocrine glands.
^Kennedy, W. R.; Wendelschafer-Crabb, G.; Brelje, T. C. (November 1994). "Innervation and vasculature of human sweat glands: an immunohistochemistry-laser scanning confocal fluorescence microscopy study". The Journal of neuroscience: the official journal of the Society for Neuroscience14 (11 pt. 2): 6825. ISSN0270-6474.
^Slatter, Douglas H., ed. (2003). Textbook of Small Animal Surgery2. Elsevier Health Sciences. p. 253. ISBN9780721686073.
^"apocrine sweat gland". Mosby's Medical Dictionary (8th ed.). Elsevier. 2009, cited in "apocrine sweat gland". The Free Dictionary. Farlex. Retrieved 6 June 2013.
^Braun-Falco, Otto; Plewig, Gerd; Wolff, Helmut H.; Burgdorf, Walter H. C. (1 January 2000). "Diseases of the Apocrine Sweat Glands". Dermatology. Springer Berlin Heidelberg. pp. 1083–1086. ISBN978-3-642-97933-0.
^Dorland's Medical Dictionary for Health Consumers. Saunders. 2007, cited in "apocrine sweat gland". The Free Dictionary. Farlex. Retrieved 6 June 2013.
^The American Heritage Medical Dictionary. Houghton Mifflin Company. 2007, cited in "apocrine sweat gland". The Free Dictionary. Farlex. Retrieved 6 June 2013.
^ abMcMurtrie, Hogin (28 November 2006). McMurtrie's Human Anatomy Coloring Book: A Systemic Approach to the Study of the Human Body: Thirteen Systems. Sterling Publishing Company, Inc. p. 430. ISBN9781402737886.
^Martin, J. J. (31 January 1984). "Neuropathological Diagnostic Methods". In Neetens, A.; Lowenthal, A.; Martin, J. J. Visual System in Myelin Disorders. The Netherlands: Springer. p. 367. ISBN9789061938071.
^Goebel, H. H.; Busch, H. (1989). "Abnormal lipopigments and lysosomal residual bodies in metachromatic leukodystrophy". Advances in experimental medicine and biology266: 299–309. ISSN0065-2598.
^Carlén, B.; Englund, E. (August 2001). "Diagnostic value of electron microscopy in a case of juvenile neuronal ceroid lipofuscinosis". Ultrastructural pathology25 (4): 285–288. ISSN0191-3123. PMID11577772.
^Elleder, M.; Jirásek, A.; Smíd, F. (19 December 1975). "Niemann-Pick disease (Crocker's type C): A histological study of the distribution and qualitative differences for the storage process". Acta Neuropathologica33 (3): 191–200. ISSN0001-6322.
^Pavelka, Margit; Roth, Jurgen (1 January 2010). Functional Ultrastructure: Atlas of Tissue Biology and Pathology. Springer. p. 332. ISBN9783211993903.
Kasture, 4 A. R.; Gokhal, S. B.; Parakh, S. R.; Paradkar (7 September 2008). Pharmaceutics-II: Second Year Diploma in Pharmacy (10 ed.). Nirali Prakashan. pp. 15.14–15.16. ISBN9788185790220.
Kurosumi, Kazumasa; Shibasaki, Susumu; Ito, Toshiho (1984). "Cytology of the Secretion in Mammalian Sweat Glands". In Bourne, Geoffrey H.; Danielli, James F. Protein Diffusion in Cell Membranes: Some Biological Implications. Orlando, Florida: Academic Press. pp. 253–330. ISBN9780123644879.
James, William D.; Berger, Timothy G.; Elston, Dirk M. (2011). Andrews' Diseases of the Skin: Clinical Dermatology (11th ed.). London: Elsevier. ISBN9781437703146.
Krstic, Radivoj V. (18 March 2004). Human Microscopic Anatomy: An Atlas for Students of Medicine and Biology. Springer. pp. 464, 466–469. ISBN9783540536666.
Rubin, Raphael; Strayer, David Sheldon (29 March 2011). Rubin's Pathology: Clinicopathologic Foundations of Medicine. Lippincott Williams & Wilkins. pp. 1043, 1048. ISBN9781605479682.