Английская Википедия:Alpha-adrenergic agonist
Шаблон:Short description Шаблон:Infobox drug class
Alpha-adrenergic agonists are a class of sympathomimetic agents that selectively stimulates alpha adrenergic receptors. The alpha-adrenergic receptor has two subclasses α1 and α2. Alpha 2 receptors are associated with sympatholytic properties. Alpha-adrenergic agonists have the opposite function of alpha blockers. Alpha adrenoreceptor ligands mimic the action of epinephrine and norepinephrine signaling in the heart, smooth muscle and central nervous system, with norepinephrine being the highest affinity. The activation of α1 stimulates the membrane bound enzyme phospholipase C, and activation of α2 inhibits the enzyme adenylate cyclase. Inactivation of adenylate cyclase in turn leads to the inactivation of the secondary messenger cyclic adenosine monophosphate and induces smooth muscle and blood vessel constriction.
Classes
Although complete selectivity between receptor agonism is rarely achieved, some agents have partial selectivity. NB: the inclusion of a drug in each category just indicates the activity of the drug at that receptor, not necessarily the selectivity of the drug (unless otherwise noted).
α1 agonist
α1 agonist: stimulates phospholipase C activity. (vasoconstriction and mydriasis; used as vasopressors, nasal decongestants and during eye exams). Selected examples are:
- Methoxamine
- Midodrine
- Metaraminol
- Phenylephrine[1]
- Amidephrine[2]
- Sdz-nvi-085 [104195-17-7].
α2 agonist
Шаблон:Main α2 agonist: inhibits adenylyl cyclase activity, reduces brainstem vasomotor center-mediated CNS activation; used as antihypertensive, sedative & treatment of opiate dependence and alcohol withdrawal symptoms). Selected examples are:
- Clonidine (mixed alpha2-adrenergic and imidazoline-I1 receptor agonist)
- Dexmedetomidine
- Fadolmidine
- Guanfacine,[3] (preference for alpha2A-subtype of adrenoceptor)
- Guanabenz (most selective agonist for alpha2-adrenergic as opposed to imidazoline-I1)
- Guanoxabenz (metabolite of guanabenz)
- Guanethidine (peripheral alpha2-receptor agonist)
- Xylazine(not for human use),[4]
- Tizanidine
- Methyldopa
- Methylnorepinephrine
- Norepinephrine[5]
- (R)-3-nitrobiphenyline is an α2C selective agonist as well as being a weak antagonist at the αШаблон:Sub and αШаблон:Sub subtypes.[6][7]
- amitraz[8]
- DetomidineШаблон:Citation needed
- Lofexidine, an α2A adrenergic receptor agonist.[9]
- Medetomidine, an α2 adrenergic agonist.[10]
Nonspecific agonist
Nonspecific agonists act as agonists at both alpha-1 and alpha-2 receptors.
- Xylometazoline[11]
- Oxymetazoline[12]
- ApraclonidineШаблон:Citation needed
- Cirazoline[13][14]
- Epinephrine[15]
Undetermined/unsorted
The following agents are also listed as agonists by MeSH.[16]
- ergotamine
- etilefrine
- indanidine
- mephentermine
- metaraminol
- methoxamine
- mivazerol
- naphazoline
- norfenefrine
- octopamine
- phenylpropanolamine
- propylhexedrine
- rilmenidine
- romifidine
- synephrine
- talipexole
Clinical significance
Alpha-adrenergic agonists, more specifically the auto receptors of alpha 2 neurons, are used in the treatment of glaucoma by decreasing the production of aqueous fluid by the ciliary bodies of the eye and also by increasing uveoscleral outflow. Medications such as clonidine and dexmedetomidine target pre-synaptic auto receptors, therefore leading to an overall decrease in norepinephrine which clinically can cause effects such as sedation, analgesia, lowering of blood pressure and bradycardia. There is also low quality evidence that they can reduce shivering post operatively.[17]
The reduction of the stress response caused by alpha 2 agonists were theorised to be beneficial peri operatively by reducing cardiac complications, however this has shown not to be clinically effective as there was no reduction in cardiac events or mortality but there was an increased incidence of hypotension and bradycardia.[18]
Alpha-2 adrenergic agonists are sometimes prescribed alone or in combination with stimulants to treat ADHD.[19]
See also
References
External links
Шаблон:Receptor agonists and antagonists Шаблон:Adrenergic agonists Шаблон:Hypnotics and sedatives
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Hsu, W. H. and Lu, Z.-X. (1984). Amitraz' induced delay of gastrointestinal transit in mice: Mediated by α2 adrenergic receptors. Drug Development Research, Volume 4 (6), 655- 680.
- ↑ Шаблон:Cite web
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Westfall Thomas C, Westfall David P, "Chapter 6. Neurotransmission: The Autonomic and Somatic Motor Nervous Systems" (Chapter). Brunton LL, Lazo JS, Parker KL: Goodman & Gilman's The Pharmacological Basis of Therapeutics, 11e: Шаблон:Cite web.
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite book
- ↑ Шаблон:MeshPharmaList
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite book
