This article is about the hormone and neurotransmitter. For the medication used in treating low blood pressure, see norepinephrine (drug).
IUPAC name (R)-4-(2-amino-1-hydroxyethyl)benzene-1,2-diol
Synonyms Noradrenaline
Abbreviation NE, NA
Sources locus coeruleus; sympathetic nervous system; adrenal medulla
Targets system-wide
Receptors α1, α2, β1, β3
Agonists sympathomimetic drugs, clonidine, isoprenaline
Antagonists Tricyclic antidepressants, Beta blockers, antipsychotics
Precursor dopamine
Synthesizing enzyme dopamine β-monooxygenase
Metabolizing enzyme MAO-A; COMT
Database links
CAS Number 51-41-2 YesY
PubChem CID: 439260
DrugBank DB00368 YesY
ChemSpider 388394 YesY
KEGG C00547 YesY

Norepinephrine (NE), also called noradrenaline (NA) or noradrenalin, is an organic chemical in the catecholamine family that functions in the brain and body as a hormone and neurotransmitter. The name "noradrenaline," derived from Latin roots meaning "at/alongside the kidneys," is more commonly used in the United Kingdom; in the United States, "norepinephrine," derived from Greek roots having that same meaning, is usually preferred.[1] "Norepinephrine" is also the international nonproprietary name given to the drug.[2] Regardless of which name is used for the substance itself, parts of the body that produce or are affected by it are referred to as noradrenergic.

In the brain, norepinephrine is produced in closely packed brain cell neurons or nuclei that are small yet exert powerful effects on other brain areas. The most important of these nuclei is the locus coeruleus, located in the pons. Outside the brain, norepinephrine is used as a neurotransmitter by sympathetic ganglia located near the spinal cord or in the abdomen, and it is also released directly into the bloodstream by the adrenal glands. Regardless of how and where it is released, norepinephrine acts on target cells by binding to and activating noradrenergic receptors located on the cell surface.

The general function of norepinephrine is to mobilize the brain and body for action. Norepinephrine release is lowest during sleep, rises during wakefulness, and reaches much higher levels during situations of stress or danger, in the so-called fight-or-flight response. In the brain, norepinephrine increases arousal and alertness, promotes vigilance, enhances formation and retrieval of memory, and focuses attention; it also increases restlessness and anxiety. In the rest of the body, norepinephrine increases heart rate and blood pressure, triggers the release of glucose from energy stores, increases blood flow to skeletal muscle, reduces blood flow to the gastrointestinal system, and inhibits voiding of the bladder and gastrointestinal motility.

A variety of medically important drugs work by altering the actions of norepinephrine systems. Norepinephrine itself is widely used as an injectable drug for the treatment of critically low blood pressure. Beta blockers, which counter some of the effects of norepinephrine, are frequently used to treat glaucoma, migraine, and a range of cardiovascular problems. Alpha blockers, which counter a different set of norepinephrine effects, are used to treat several cardiovascular and psychiatric conditions. Alpha-2 agonists often have a sedating effect, and are commonly used as anesthesia-enhancers in surgery, as well as in treatment of drug or alcohol dependence. Many important psychiatric drugs exert strong effects on norepinephrine systems in the brain, resulting in side-effects that may be helpful or harmful.


Norepinephrine is a catecholamine and a phenethylamine.[3] Its structure differs from that of epinephrine only in that epinephrine has a methyl group attached to its nitrogen, whereas the methyl group is replaced by a hydrogen atom in norepinephrine.[3] The prefix nor- is derived as an abbreviation of the word "normal", used to indicate a demethylated compound.[4]

Chemical diagram of the structure of a norepinephrine molecule.
Norepinephrine structure
Chemical diagram of the structure of an epinephrine molecule.
Epinephrine structure
Chemical diagram of a catechol structure.
Catechol structure

Biochemical mechanisms


Biosynthetic pathways for catecholamines and trace amines in the human brain[5][6][7]
Graphic of trace amine and catecholamine metabolism
The image above contains clickable links
Norepinephrine is synthesized from dopamine in the human body by the dopamine β-hydroxylase (DBH) enzyme.

Norepinephrine is synthesized from the amino acid tyrosine by a series of enzymatic steps in the adrenal medulla and postganglionic neurons of the sympathetic nervous system. While the conversion of tyrosine to dopamine occurs predominantly in the cytoplasm, the conversion of dopamine to norepinephrine by dopamine β-monooxygenase occurs predominantly inside neurotransmitter vesicles.[8] The metabolic pathway is:

Phenylalanine → Tyrosine → L-DOPA → Dopamine → Norepinephrine[8]

Thus the direct precursor of norepinephrine is dopamine, which is synthesized indirectly from the essential amino acid phenylalanine or the non-essential amino acid tyrosine.[8] These amino acids are found in nearly every protein and, as such, are provided by ingestion of protein-containing food, with tyrosine being the most common.

Phenylalanine is converted into tyrosine by the enzyme phenylalanine hydroxylase, with molecular oxygen (O2) and tetrahydrobiopterin as cofactors. Tyrosine is converted into L-DOPA by the enzyme tyrosine hydroxylase, with tetrahydrobiopterin, O2, and probably ferrous iron (Fe2+) as cofactors.[8] L-DOPA is converted into dopamine by the enzyme aromatic L-amino acid decarboxylase (also known as DOPA decarboxylase), with pyridoxal phosphate as cofactor.[8] Dopamine is then converted into norepinephrine by the enzyme dopamine β-monooxygenase (formerly known as dopamine β-hydroxylase), with O2 and ascorbic acid as cofactors.[8]

Norepinephrine itself can further be converted into epinephrine by the enzyme phenylethanolamine N-methyltransferase with S-adenosyl-L-methionine as cofactor.[8]


In mammals, norepinephrine is rapidly degraded to various metabolites. The initial step in the breakdown can be catalyzed by either of the enzymes monoamine oxidase (mainly monoamine oxidase A) or COMT.[9] From there the breakdown can proceed by a variety of pathways. The principal end products are either Vanillylmandelic acid or a conjugated form of MHPG, both of which are thought to be biologically inactive and are excreted in the urine.[10]

Norepinephrine degradation.[10] Metabolizing enzymes are shown in boxes.


Cellular effects

Main article: Adrenergic receptor
Adrenergic receptors in the mammal brain and body[10]
Family Receptor Type Mechanism
Alpha α1 Gq-coupled. Increase IP3 and calcium by
activating phospholipase C.
α2 Gi/Go-coupled. Decrease cAMP by
inhibiting adenylate cyclase.
Beta β1 Gs-coupled. Increase cAMP by
activating adenylate cyclase.

Like many other biologically active substances, norepinephrine exerts its effects by binding to and activating receptors located on the surface of cells. Two broad families of norepinephrine receptors have been identified, known as alpha and beta adrenergic receptors.[10] Alpha receptors are divided into subtypes α1 and α2; beta receptors into subtypes β1, β2, and β3.[10] All of these function as G protein-coupled receptors, meaning that they exert their effects via a complex second messenger system.[10] Alpha-2 receptors usually have inhibitory effects, but many are located pre-synaptically (i.e., on the surface of the cells that release norepinephrine), so the net effect of alpha-2 activation is often a decrease in the amount of norepinephrine released.[10] Alpha-1 receptors and all three types of beta receptors usually have excitatory effects.[10]

Storage, release, and reuptake

Cartoon diagram of a noradrenergic synapse, showing the synthetic and metabolic mechanisms as well as the things that can happen after release.
Norepinephrine (labeled "noradrenaline" in this drawing) processing in a synapse. After release norepinephrine can either be taken up again by the presynaptic terminal, or broken down by enzymes.

Inside the brain norepinephrine functions as a neurotransmitter, and is controlled by a set of mechanisms common to all monoamine neurotransmitters. After synthesis, norepinephrine is transported from the cytosol into synaptic vesicles by the vesicular monoamine transporter (VMAT).[11] Norepinephrine is stored in these vesicles until it is ejected into the synaptic cleft, typically after an action potential causes the vesicles to release their contents directly into the synaptic cleft through a process called exocytosis.[10]

Once in the synapse, norepinephrine binds to and activates receptors. After an action potential, the norepinephrine molecules quickly become unbound from their receptors. They are then absorbed back into the presynaptic cell, via reuptake mediated primarily by the norepinephrine transporter (NET).[12] Once back in the cytosol, norepinephrine can either be broken down by monoamine oxidase or repackaged into vesicles by VMAT, making it available for future release.[11]

Sympathetic nervous system

Schema of the sympathetic nervous system, showing the sympathetic ganglia and the parts of the body to which they connect.

Norepinephrine is the main neurotransmitter used by the sympathetic nervous system, which consists of about two dozen sympathetic chain ganglia located next to the spinal cord, plus a set of prevertebral ganglia located in the chest and abdomen.[13] These sympathetic ganglia are connected to numerous organs, including the eyes, salivary glands, heart, lungs, liver, gallbladder, stomach, intestines, kidneys, urinary bladder, reproductive organs, muscles, skin, and adrenal glands.[13] Sympathetic activation of the adrenal glands causes the part called the adrenal medulla to release norepinephrine into the bloodstream, from which, functioning as a hormone, it gains further access to a wide variety of tissues.[13]

Broadly speaking, the effect of norepinephrine on each target organ is to modify its state in a way that makes it more conducive to active body movement, often at a cost of increased energy use and increased wear and tear.[14] This can be contrasted with the acetylcholine-mediated effects of the parasympathetic nervous system, which modifies most of the same organs into a state more conducive to rest, recovery, and digestion of food, and usually less costly in terms of energy expenditure.[14]

The sympathetic effects of norepinephrine include:

Central nervous system

Brain areas containing noradrenergic neurons.

The noradrenergic neurons in the brain form a neurotransmitter system, that, when activated, exerts effects on large areas of the brain. The effects are manifested in alertness, arousal, and readiness for action.

Noradrenergic neurons (i.e., neurons whose primary neurotransmitter is norepinephrine) are comparatively few in number, and their cell bodies are confined to a few relatively small brain areas, but they send projections to many other brain areas and exert powerful effects on their targets. These noradrenergic cell groups were first mapped in 1964 by Annica Dahlström and Kjell Fuxe, who assigned them labels starting with the letter "A" (for "aminergic").[22] In their scheme, areas A1 through A7 contain the neurotransmitter norepinephrine (A8 through A14 contain dopamine). Noradrenergic cell group A1 is located in the caudal ventrolateral part of the medulla, and plays a role in the control of body fluid metabolism.[23] Noradrenergic cell group A2 is located in a brainstem area called the solitary nucleus; these cells have been implicated in a variety of responses, including control of food intake and responses to stress.[24] Cell groups A5 and A7 project mainly to the spinal cord.[25]

The most important source of norepinephrine in the brain is the locus coeruleus, which contains noradrenergic cell group A6 and adjoins cell group A4. The locus coeruleus is quite small in absolute terms—in primates it is estimated to contain around 15,000 neurons, less than one millionth of the neurons in the brain—but it sends projections to every major part of the brain and also to the spinal cord.[26]

The level of activity in the locus coeruleus correlates broadly with vigilance and speed of reaction. LC activity is low during sleep and drops to virtually nothing during the REM (dreaming) state.[27] It runs at a baseline level during wakefulness, but increases temporarily when a person is presented with any sort of stimulus that draws attention. Unpleasant stimuli such as pain, difficulty breathing, bladder distension, heat or cold generate larger increases. Extremely unpleasant states such as intense fear or intense pain are associated with very high levels of LC activity.[26]

Norepinephrine released by the locus coeruleus affects brain function in a number of ways. It enhances processing of sensory inputs, enhances attention, enhances formation and retrieval of both long term and working memory, and enhances the ability of the brain to respond to inputs by changing the activity pattern in the prefrontal cortex and other areas.[28] The control of arousal level is strong enough that drug-induced suppression of the LC has a powerful sedating effect.[27]

There is great similarity between situations that activate the locus coeruleus in the brain and situations that activate the sympathetic nervous system in the periphery: the LC essentially mobilizes the brain for action while the sympathetic system mobilizes the body. It has been argued that this similarity arises because both are to a large degree controlled by the same brain structures, particularly a part of the brainstem called the nucleus gigantocellularis.[26]


A large number of important drugs exert their effects by interacting with norepinephrine systems in the brain or body. Their uses include treatment of cardiovascular problems, shock, and a variety of psychiatric conditions.

Sympathomimetic and sympatholytic drugs

Sympathomimetic drugs mimic or enhance at least some of the effects of norepinephrine released by the sympathetic nervous system; sympatholytic drugs, in contrast, block at least some of the effects.[29] Both of these are large groups with diverse uses, depending on exactly which effects are enhanced or blocked.[29] Norepinephrine itself is classified as a sympathomimetic drug: its effects when given by intravenous injection of increasing heart rate and force and constricting blood vessels make it very useful for treating medical emergencies that involve critically low blood pressure.[29]

Beta blockers

Main article: Beta blocker

These are drugs that block the effects of beta noradrenergic receptors while having little or no effect on alpha receptors. They are sometimes used to treat high blood pressure, atrial fibrillation and congestive heart failure, but recent reviews have concluded that other types of drugs are usually superior for those purposes.[30][31] Beta blockers may be a viable choice for other cardiovascular conditions, though, including angina and Marfan syndrome.[32] They are also widely used to treat glaucoma, either in pill form or in eyedrops.[33] Because of their effects in reducing anxiety symptoms and tremor, they have sometimes been used by entertainers, public speakers and athletes to reduce performance anxiety, although they are not medically approved for that purpose and are banned by the International Olympic Committee.[34][35]

Unfortunately, the usefulness of beta blockers is limited by a range of serious side effects, including slowing of heart rate, a drop in blood pressure, asthma, and reactive hypoglycemia.[33] The negative effects can be particularly severe in people who suffer from diabetes.[30]

Alpha blockers

Main article: Alpha blocker

These are drugs that block the effects of noradrenergic alpha receptors while having little or no effect on beta receptors.[36] Drugs belonging to this group can have very different effects, however, depending on whether they primarily block alpha-1 receptors, alpha-2 receptors, or both. Alpha-2 receptors, as described elsewhere in this article, are frequently located on norepinephrine-releasing neurons themselves and have inhibitory effects on them; consequently blockage of alpha-2 receptors usually results in an increase in norepinephrine release.[36] Alpha-1 receptors are usually located on target cells and have excitatory effects on them; consequently blockage of alpha-1 receptors usually results in blocking some of the effects of norepinephrine.[36] Drugs such as phentolamine that act on both types of receptors can produce a complex combination of both effects. In most cases when the term "alpha blocker" is used without qualification, it refers to a selective alpha-1 antagonist.

Selective alpha-1 blockers have a variety of uses. Because one of their effects is to relax the muscles in the neck of the bladder, they are often used to treat benign prostatic hyperplasia, and to help with the expulsion of bladder stones.[37] Their effects on the central nervous system make them useful for treating generalized anxiety disorder, panic disorder, and posttraumatic stress disorder.[38] They may, however, have significant side-effects, including a drop in blood pressure.[36]

Some antidepressants function partly as selective alpha-2 blockers, but the best-known drug in that class is yohimbine, which is extracted from the bark of the African yohimbe tree.[39] Yohimbine acts as a male potency enhancer, but its usefulness for that purpose is limited by serious side-effects including anxiety and insomnia.[39] Overdoses can cause a dangerous increase in blood pressure.[39] Yohimbine is banned in many countries, but in the United States, because it is extracted from a plant rather than chemically synthesized, it is sold over the counter as a nutritional supplement.[40]

Alpha-2 agonists

These are drugs that activate alpha-2 receptors or enhance their effects. Because alpha-2 receptors are inhibitory and many are located presynaptically on norepinephrine-releasing cells, the net effect of these drugs is usually to reduce the amount of norepinephrine released.[41] Drugs in this group that are capable of entering the brain often have strong sedating effects, due to their inhibitory effects on the locus coeruleus.[41] Clonidine, for example, is used for the treatment of anxiety disorders and insomnia, and also as a sedative premedication for patients about to undergo surgery.[42] Xylazine, another drug in this group, is also a powerful sedative and is often used in combination with ketamine as a general anaesthetic for veterinary surgery—in the United States it has not been approved for use in humans.[43]

Stimulants and antidepressants

These are drugs whose primary effects are thought to be mediated by different neurotransmitter systems (dopamine for stimulants, serotonin for antidepressants), but many also increase levels of norepinephrine in the brain. Amphetamine, for example, is a stimulant that increases release of norepinephrine as well as dopamine. Monoamine oxidase inhibitors are antidepressants that inhibit the metabolic degradation of norepinephrine as well as serotonin. In some cases it is difficult to distinguish the norepinephrine-mediated effects from the effects related to other neurotransmitters.

Diseases and disorders

A number of important medical problems involve dysfunction of the norepinephrine system in the brain or body.

Sympathetic hyperactivation

Hyperactivation of the sympathetic nervous system is not a recognized condition in itself, but it is a component of a number of conditions, as well as a possible consequence of taking sympathomimetic drugs. It causes a distinctive set of symptoms including aches and pains, rapid heartbeat, elevated blood pressure, sweating, palpitations, anxiety, headache, paleness, and a drop in blood glucose. If sympathetic activity is elevated for an extended time, it can cause weight loss and other stress-related body changes.

The list of conditions that can cause sympathetic hyperactivation includes severe brain injury,[44] spinal cord damage,[45] heart failure,[46] high blood pressure,[47] kidney disease,[48] and various types of stress.


A pheochromocytoma is a rarely occurring tumor of the adrenal medulla, caused either by genetic factors or certain types of cancer. The consequence is a massive increase in the amount of norepinephrine and epinephrine released into the bloodstream. The most obvious symptoms are those of sympathetic hyperactivation, including particularly a rise in blood pressure that can reach fatal levels. The most effective treatment is surgical removal of the tumor.


Stress, to a physiologist, means any situation that threatens the continued stability of the body and its functions.[49] Stress affects a wide variety of body systems: the two most consistently activated are the hypothalamic-pituitary-adrenal axis and the norepinephrine system, including both the sympathetic nervous system and the locus coeruleus-centered system in the brain.[49] Stressors of many types evoke increases in noradrenergic activity, which mobilizes the brain and body to meet the threat.[49] Chronic stress, if continued for a long time, can damage many parts of the body. A significant part of the damage is due to the effects of sustained norepinephrine release, because of norepinephrine's general function of directing resources away from maintenance, regeneration, and reproduction, and toward systems that are required for active movement. The consequences can include slowing of growth (in children), sleeplessness, loss of libido, gastrointestinal problems, impaired disease resistance, slower rates of injury healing, depression, and increased vulnerability to addiction.[49]


Attention deficit hyperactivity disorder is a psychiatric condition involving problems with attention, hyperactivity, and impulsiveness.[50] It is most commonly treated using stimulant drugs such as methylphenidate (Ritalin), whose primary effect is to increase dopamine levels in the brain, but drugs in this group also generally increase brain levels of norepinephrine, and it has been difficult to determine whether these actions are involved in their clinical value. Also there is substantial evidence that many people with ADHD show "biomarkers" involving altered norepinephrine processing.[51] Several drugs whose primary effects are on norepinephrine, including guanfacine, clonidine, and atomoxetine, have been tried as treatments for ADHD, and found to have effects comparable to those of stimulants.[52][53]

Autonomic failure

Several conditions, including Parkinson's disease, diabetes and so-called pure autonomic failure, can cause a loss of norepinephrine-secreting neurons in the sympathetic nervous system. The symptoms are widespread, the most serious being a reduction in heart rate and an extreme drop in resting blood pressure, making it impossible for severely affected people to stand for more than a few seconds without fainting. Treatment can involve dietary changes or drugs.[54]

Comparative biology and evolution

Chemical structure of octopamine, which serves as the homologue of norepinephrine in many invertebrate species

Norepinephrine has been reported to exist in a wide variety of animal species, including protozoa,[55] placozoa and cnidaria (jellyfish and related species),[56] but not in ctenophores (comb jellies), whose nervous systems differ greatly from those of other animals.[57] It is generally present in deuterostomes (vertebrates, etc.), but in protostomes (arthropods, molluscs, flatworms, nematodes, annelids, etc.) it is replaced by octopamine, a closely related chemical with a closely related synthesis pathway.[55] In insects, octopamine has alerting and activating functions that correspond (at least roughly) with the functions of norepinephrine in vertebrates.[58] It has been argued that octopamine evolved to replace norepinephrine rather than vice versa; however, the nervous system of amphioxus (a primitive chordate) has been reported to contain octopamine but not norepinephrine, which presents difficulties for that hypothesis.[55]


Early in the twentieth century Walter Cannon, who had popularized the idea of a sympatho-adrenal system preparing the body for fight and flight, and his colleague Arturo Rosenblueth developed a theory of two sympathins, sympathin E (excitatory) and sympathin I (inhibitory), responsible for these actions.[59] The Belgian pharmacologist Zénon Bacq as well as Canadian and US-American pharmacologists between 1934 and 1938 suggested that noradrenaline might be a sympathetic transmitter.[59] In 1939, Hermann Blaschko and Peter Holtz independently identified the biosynthetic mechanism for norepinephrine in the vertebrate body.[60][61] In 1945 Ulf von Euler published the first of a series of papers that established the role of norepinephrine as a neurotransmitter.[62] He demonstrated the presence of norepinephrine in sympathetically innervated tissues and brain, and adduced evidence that it is the sympathin of Cannon and Rosenblueth.


  1. Aronson JK (Feb 2000). ""Where name and image meet"--the argument for "adrenaline"". British Medical Journal. 320 (7233): 506–9. doi:10.1136/bmj.320.7233.506. PMC 1127537Freely accessible. PMID 10678871.
  2. "(-)-noradrenaline". IUPHAR database. International Union of Basic and Clinical Pharmacology. Retrieved 2 January 2016.
  3. 1 2 "Norepinephrine". PubChem. Retrieved 6 November 2015.
  4. Gaddum JH (June 1956). "The Prefix 'Nor' in Chemical Nomenclature". Nature. 177 (1046): 1046–1046. Bibcode:1956Natur.177.1046G. doi:10.1038/1771046b0.
  5. Broadley KJ (March 2010). "The vascular effects of trace amines and amphetamines". Pharmacol. Ther. 125 (3): 363–375. doi:10.1016/j.pharmthera.2009.11.005. PMID 19948186.
  6. Lindemann L, Hoener MC (May 2005). "A renaissance in trace amines inspired by a novel GPCR family". Trends Pharmacol. Sci. 26 (5): 274–281. doi:10.1016/ PMID 15860375.
  7. Wang X, Li J, Dong G, Yue J (February 2014). "The endogenous substrates of brain CYP2D". Eur. J. Pharmacol. 724: 211–218. doi:10.1016/j.ejphar.2013.12.025. PMID 24374199. The highest level of brain CYP2D activity was found in the substantia nigra (Bromek et al., 2010). The in vitro and in vivo studies have shown the contribution of the alternative CYP2D-mediated dopamine synthesis to the concentration of this neurotransmitter although the classic biosynthetic route to dopamine from tyrosine is active. CYP2D6 protein level is approximately 40% lower in the frontal cortex, cerebellum, and hippocampus in PD patients, even when controlling for CYP2D6 genotype (Mann et al., 2012). ... Tyramine levels are especially high in the basal ganglia and limbic system, which are thought to be related to individual behavior and emotion (Yu et al., 2003c). Studies have demonstrated that dopamine is formed from p-tyramine as well as m-tyramine via tyramine 3-hydroxylation or 4-hydroxylation by rat CYP2D2, 2D4, and 2D18 as well as human CYP2D6. ... Both rat CYP2D and human CYP2D6 have a higher affinity for m-tyramine compared with p-tyramine for the generation of dopamine. Rat CYP2D isoforms (2D2/2D4/2D18) are less efficient than human CYP2D6 for the generation of dopamine from p-tyramine. The Km values of the CYP2D isoforms are as follows: CYP2D6 (87–121 μm) ≈ CYP2D2 ≈ CYP2D18 > CYP2D4 (256 μm) for m-tyramine and CYP2D4 (433 μm) > CYP2D2 ≈ CYP2D6 > CYP2D18 (688 μm) for p-tyramine (Bromek et al., 2010; Thompson et al., 2000).
  8. 1 2 3 4 5 6 7 Musacchio JM (2013). "Chapter 1: Enzymes involved in the biosynthesis and degradation of catecholamines". In Iverson L. Biochemistry of Biogenic Amines. Springer. pp. 1–35. ISBN 1-4684-3171-4.
  9. Griffith RK (2013). "Chapter 10: Adrenergic Receptors and Drugs Affecting Adrenergic Neurotransmission". In Lemke TL, Williams DA, Zito SW, Roche VF. Foye's Principles of Medicinal Chemistry (7th ed.). Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. p. 343. ISBN 978-1-60913-345-0.
  10. 1 2 3 4 5 6 7 8 9 Rang HP, Ritter JM, Flower R, Henderson G (2014). "Chapter 14: Noradrenergic transmission". Rang & Dale's Pharmacology. Elsevier Health Sciences. pp. 177–196. ISBN 978-0-7020-5497-6.
  11. 1 2 Eiden LE, Schäfer MK, Weihe E, Schütz B (2004). "The vesicular amine transporter family (SLC18): amine/proton antiporters required for vesicular accumulation and regulated exocytotic secretion of monoamines and acetylcholine". Pflugers Arch. 447 (5): 636–40. doi:10.1007/s00424-003-1100-5. PMID 12827358.
  12. Torres GE, Gainetdinov RR, Caron MG (2003). "Plasma membrane monoamine transporters: structure, regulation and function". Nature Reviews Neuroscience. 4 (1): 13–25. doi:10.1038/nrn1008. PMID 12511858.
  13. 1 2 3 Hamill RW, Shapiro RE, Vizzard MA (2012). "Peripheral Autonomic Nervous System". In Robertson D, Biaggioni I, et al.. Primer on the Autonomic Nervous System. Academic Press. pp. 17–20. ISBN 978-0-12-386525-0.
  14. 1 2 Schacter D, Gilbert D, Wegner D, Hood B (2011). Psychology: European Edition. Palgrave Macmillan. p. 93. ISBN 978-0-230-34367-2.
  15. Dartt DA (May 2009). "Neural regulation of lacrimal gland secretory processes: relevance in dry eye diseases". Progress in Retinal and Eye Research. 28 (3): 155–77. doi:10.1016/j.preteyeres.2009.04.003. PMC 3652637Freely accessible. PMID 19376264.
  16. Tank AW, Lee Wong D (January 2015). "Peripheral and central effects of circulating catecholamines". Comprehensive Physiology. 5 (1): 1–15. doi:10.1002/cphy.c140007. PMID 25589262.
  17. Bahler L, Molenaars RJ, Verberne HJ, Holleman F (September 2015). "Role of the autonomic nervous system in activation of human brown adipose tissue: A review of the literature". Diabetes & Metabolism. 41: 437–445. doi:10.1016/j.diabet.2015.08.005. PMID 26404650.
  18. Kenney MJ, Ganta CK (July 2014). "Autonomic nervous system and immune system interactions". Comprehensive Physiology. 4 (3): 1177–200. doi:10.1002/cphy.c130051. PMC 4374437Freely accessible. PMID 24944034.
  19. Chistiakov DA, Ashwell KW, Orekhov AN, Bobryshev YV (2015). "Innervation of the arterial wall and its modification in atherosclerosis". Auton Neurosci. 193: 7–11. doi:10.1016/j.autneu.2015.06.005. PMID 26164815.
  20. 1 2 3 4 5 Thorp AA, Schlaich MP (2015). "Relevance of Sympathetic Nervous System Activation in Obesity and Metabolic Syndrome". J Diabetes Res. 2015: 341583. doi:10.1155/2015/341583. PMC 4430650Freely accessible. PMID 26064978.
  21. Konturek SJ, Konturek JW, Pawlik T, Brzozowski T (2004). "Brain-gut axis and its role in the control of food intake" (PDF). J. Physiol. Pharmacol. 55 (1 Pt 2): 137–54. PMID 15082874.
  22. Dahlstroem A, Fuxe K (1964). "Evidence for the existence of monoamine-containing neurons in the central nervous system. I. Demonstration of monoamines in the cell bodies of brain stem neurons". Acta Physiologica Scandinavica. Supplementum. 232 (Supplement 232): 1–55. PMID 14229500.
  23. Antunes-Rodrigues J, de Castro M, Elias LL, Valença MM, McCann SM (January 2004). "Neuroendocrine control of body fluid metabolism". Physiological Reviews. 84 (1): 169–208. doi:10.1152/physrev.00017.2003. PMID 14715914.
  24. Rinaman L (February 2011). "Hindbrain noradrenergic A2 neurons: diverse roles in autonomic, endocrine, cognitive, and behavioral functions". American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 300 (2): R222–35. doi:10.1152/ajpregu.00556.2010. PMC 3043801Freely accessible. PMID 20962208.
  25. Bruinstroop E, Cano G, Vanderhorst VG, Cavalcante JC, Wirth J, Sena-Esteves M, Saper CB (June 2012). "Spinal projections of the A5, A6 (locus coeruleus), and A7 noradrenergic cell groups in rats". The Journal of Comparative Neurology. 520 (9): 1985–2001. doi:10.1002/cne.23024. PMC 3508755Freely accessible. PMID 22173709.
  26. 1 2 3 Sara SJ, Bouret S (2012). "Orienting and reorienting: the locus coeruleus mediates cognition through arousal". Neuron. 76 (1): 130–41. doi:10.1016/j.neuron.2012.09.011. PMID 23040811.
  27. 1 2 Berridge CW, Schmeichel BE, España RA (2012). "Noradrenergic modulation of wakefulness/arousal". Sleep Med Rev. 16 (2): 187–97. doi:10.1016/j.smrv.2011.12.003. PMC 3278579Freely accessible. PMID 22296742.
  28. Sara SJ (2015). "Locus Coeruleus in time with the making of memories". Curr. Opin. Neurobiol. 35: 87–94. doi:10.1016/j.conb.2015.07.004. PMID 26241632.
  29. 1 2 3 Gardenhire DS (2013). Rau's Respiratory Care Pharmacology. Elsevier Health Sciences. p. 88. ISBN 978-0-323-27714-3.
  30. 1 2 Deedwania PC (2015). "Management of Patients With Stable Angina and Type 2 Diabetes". Rev Cardiovasc Med. 16 (2): 105–13. PMID 26198557.
  31. Mareev Y, Cleland JG (2015). "Should β-Blockers Be Used in Patients With Heart Failure and Atrial Fibrillation?". Clin Ther. 37: 2215–24. doi:10.1016/j.clinthera.2015.08.017. PMID 26391145.
  32. Kumar A, Agarwal S (2014). "Marfan syndrome: An eyesight of syndrome". Meta Gene. 2: 96–105. doi:10.1016/j.mgene.2013.10.008. PMC 4287801Freely accessible. PMID 25606393.
  33. 1 2 Inoue K (2014). "Managing adverse effects of glaucoma medications". Clin Ophthalmol. 8: 903–13. doi:10.2147/OPTH.S44708. PMC 4025938Freely accessible. PMID 24872675.
  34. Brugués AO (2011). "Music performance anxiety-part 2. a review of treatment options". Med Probl Perform Art. 26 (3): 164–71. PMID 21987072.
  35. Fitch K (2012). "Proscribed drugs at the Olympic Games: permitted use and misuse (doping) by athletes". Clin Med. 12 (3): 257–60. doi:10.7861/clinmedicine.12-3-257. PMID 22783779.
  36. 1 2 3 4 Lilley LL, Collins SR, Snyder JS (2014). Pharmacology and the Nursing Process, 7th edition. Elsevier Health Sciences. pp. 313–316. ISBN 978-0-323-29361-7.
  37. Campschroer T, Zhu Y, Duijvesz D, Grobbee DE, Lock MT (2014). "Alpha-blockers as medical expulsive therapy for ureteral stones". Cochrane Database Syst Rev. 4: CD008509. doi:10.1002/14651858.CD008509.pub2. PMID 24691989.
  38. Green B (2014). "Prazosin in the treatment of PTSD". J Psychiatr Pract. 20 (4): 253–9. doi:10.1097/01.pra.0000452561.98286.1e. PMID 25036580.
  39. 1 2 3 Corazza O, Martinotti G, Santacroce R, Chillemi E, Di Giannantonio M, Schifano F, Cellek S (2014). "Sexual enhancement products for sale online: raising awareness of the psychoactive effects of yohimbine, maca, horny goat weed, and Ginkgo biloba". Biomed Res Int. 2014: 841798. doi:10.1155/2014/841798. PMC 4082836Freely accessible. PMID 25025070.
  40. EFSA Panel on Food Additives and Nutrient Sources Added to Food (2013). "Scientific Opinion on the evaluation of the safety in use of Yohimbe" (PDF). EFSA Journal. 11 (7): 3302.
  41. 1 2 Lemke KA (2004). "Perioperative use of selective alpha-2 agonists and antagonists in small animals". Can. Vet. J. 45 (6): 475–80. PMC 548630Freely accessible. PMID 15283516.
  42. Belkin MR, Schwartz TL (2015). "Alpha-2 receptor agonists for the treatment of posttraumatic stress disorder". Drugs Context. 4: 212286. doi:10.7573/dic.212286. PMC 4544272Freely accessible. PMID 26322115.
  43. Greene SA, Thurmon JC (1988). "Xylazine—a review of its pharmacology and use in veterinary medicine". J. Vet. Pharmacol. Ther. 11 (4): 295–313. doi:10.1111/j.1365-2885.1988.tb00189.x. PMID 3062194.
  44. Lump D, Moyer M (2014). "Paroxysmal sympathetic hyperactivity after severe brain injury". Curr Neurol Neurosci Rep. 14 (11): 494. doi:10.1007/s11910-014-0494-0. PMID 25220846.
  45. Amzallag M (1993). "Autonomic hyperreflexia". Int Anesthesiol Clin. 31 (1): 87–102. doi:10.1097/00004311-199331010-00009. PMID 8440534.
  46. McCrink KA, Brill A, Lymperopoulos A (2015). "Adrenal G protein-coupled receptor kinase-2 in regulation of sympathetic nervous system activity in heart failure". World J Cardiol. 7 (9): 539–43. doi:10.4330/wjc.v7.i9.539. PMID 26413230.
  47. Malpas SC (2010). "Sympathetic nervous system overactivity and its role in the development of cardiovascular disease". Physiol. Rev. 90 (2): 513–57. doi:10.1152/physrev.00007.2009. PMID 20393193.
  48. Ksiazek A, Załuska W (2008). "Sympathetic overactivity in uremia". J Ren Nutr. 18 (1): 118–21. doi:10.1053/j.jrn.2007.10.024. PMID 18089457.
  49. 1 2 3 4 Chrousos GP (2009). "Stress and disorders of the stress system" (PDF). Nat Rev Endocrinol. 5 (7): 374–81. doi:10.1038/nrendo.2009.106. PMID 19488073.
  50. Kooij SJ, Bejerot S et al. (2010). "European consensus statement on diagnosis and treatment of adult ADHD: The European Network Adult ADHD". BMC Psychiatry. 10: 67. doi:10.1186/1471-244X-10-67. PMC 2942810Freely accessible. PMID 20815868.
  51. Faraone SV, Bonvicini C, Scassellati C (2014). "Biomarkers in the diagnosis of ADHD--promising directions". Curr Psychiatry Rep. 16 (11): 497. doi:10.1007/s11920-014-0497-1. PMID 25298126.
  52. Bello NT (2015). "Clinical utility of guanfacine extended release in the treatment of ADHD in children and adolescents". Patient Prefer Adherence. 9: 877–85. doi:10.2147/PPA.S73167. PMC 4494608Freely accessible. PMID 26170637.
  53. Clemow DB, Bushe CJ (2015). "Atomoxetine in patients with ADHD: A clinical and pharmacological review of the onset, trajectory, duration of response and implications for patients". J. Psychopharmacol. (Oxford). 29: 1221–30. doi:10.1177/0269881115602489. PMID 26349559.
  54. Shibao C, Okamoto L, Biaggioni I (2012). "Pharmacotherapy of autonomic failure". Pharmacol. Ther. 134 (3): 279–86. doi:10.1016/j.pharmthera.2011.05.009. PMC 3358114Freely accessible. PMID 21664375.
  55. 1 2 3 Pflüger HJ, Stevensonb PA (2005). "Evolutionary aspects of octopaminergic systems with emphasis on arthropods" (PDF). Arthropod Structure & Development. 34: 379–396. doi:10.1016/j.asd.2005.04.004.
  56. Kass-Simon G, Pierobon P (2007). "Cnidarian chemical neurotransmission, an updated overview". Comp. Biochem. Physiol., Part A Mol. Integr. Physiol. 146 (1): 9–25. doi:10.1016/j.cbpa.2006.09.008. PMID 17101286.
  57. Moroz LL (2015). "Convergent evolution of neural systems in ctenophores". J. Exp. Biol. 218 (Pt 4): 598–611. doi:10.1242/jeb.110692. PMID 25696823.
  58. Verlinden H, Vleugels R, Marchal E, Badisco L, Pflüger HJ, Blenau W, Broeck JV (2010). "The role of octopamine in locusts and other arthropods". J. Insect Physiol. 56 (8): 854–67. doi:10.1016/j.jinsphys.2010.05.018. PMID 20621695.
  59. 1 2 Bacq ZM (1983). "Chemical transmission of nerve impulses". In Parnham MJ, Bruinvels J. Discoveries in Pharmacology, Volume 1. Amsterdam: Elsevier. pp. 49–103. ISBN 0-444-80493-5.
  60. Herman Blaschko (1987). "A half-century of research on catecholamine biosynthesis". Journal of Applied Cardiology: 171–183.
  61. P. Holtz (1939). "Dopadecarboxylase". Die Naturwissenschaften (in German). 27: 724–725. doi:10.1007/bf01494245.
  62. von Euler US (1945). "A sympathomimetic pressor substance in animal organ extracts". Nature. 156: 18–19. doi:10.1038/156018b0.
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