Alpha-2 adrenergic receptor agonist
An overview of alpha-2 adrenergic receptor agonists, their mechanisms, uses, and related topics.
Alpha-2 adrenergic receptor agonists are a class of pharmacological agents that primarily act on the alpha-2 adrenergic receptors in the central nervous system and peripheral nervous system. These receptors are part of the adrenergic receptor family, which are G protein-coupled receptors involved in the regulation of various physiological processes.
Mechanism of Action[edit | edit source]
Alpha-2 adrenergic receptors are located both pre- and post-synaptically. When activated by an agonist, these receptors inhibit the release of norepinephrine and other neurotransmitters, leading to a decrease in sympathetic nervous system activity. This results in effects such as reduced blood pressure, sedation, and analgesia.
Clinical Uses[edit | edit source]
Alpha-2 adrenergic receptor agonists are used in a variety of clinical settings:
- Hypertension: Drugs like clonidine and methyldopa are used to lower blood pressure by reducing sympathetic outflow from the central nervous system.
- Sedation and Anesthesia: Dexmedetomidine is used for its sedative properties in intensive care settings and during surgical procedures.
- Attention Deficit Hyperactivity Disorder (ADHD): Guanfacine and clonidine are used as adjunctive treatments for ADHD.
- Opioid Withdrawal: Clonidine is sometimes used to alleviate withdrawal symptoms in patients undergoing opioid detoxification.
Side Effects[edit | edit source]
Common side effects of alpha-2 adrenergic receptor agonists include:
Examples of Alpha-2 Adrenergic Receptor Agonists[edit | edit source]
Also see[edit | edit source]
Template:Receptor pharmacology
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