Adrenergic receptor/Related Articles: Difference between revisions
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{{r|Adrenergic beta-antagonist}} | {{r|Adrenergic beta-antagonist}} | ||
{{r|Adrenergic uptake inhibitor}} | {{r|Adrenergic uptake inhibitor}} | ||
==Articles related by keyphrases (Bot populated)== | |||
{{r|Beta-2 adrenergic receptor}} | |||
{{r|G-protein-coupled receptor kinase}} |
Latest revision as of 17:00, 6 July 2024
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- See also changes related to Adrenergic receptor, or pages that link to Adrenergic receptor or to this page or whose text contains "Adrenergic receptor".
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Subtopics
- Adrenal gland [r]: A pair of glands located at the cranial pole of each of the two kidneys. Each adrenal gland is composed of two distinct endocrine tissues with separate embryonic origins, the adrenal cortex producing glucocorticoids and mineralocorticoids and the adrenal medulla producing neurotransmitters. [e]
- Adrenal insufficiency [r]: Adrenocortical insufficiency caused by disease, suppression by drugs, destruction, or surgical removal of the adrenal cortices. [e]
- Adrenergic agent [r]: Drugs that act on adrenergic receptors or affect the life cycle of adrenergic transmitters. [e]
- Adrenergic beta-agonist [r]: Class of drugs used to treat asthma and other pulmonary disease states. [e]
- Adrenergic beta-antagonist [r]: Drugs that bind to but do not activate beta-adrenergic receptors thereby blocking the actions of beta-adrenergic agonists. Adrenergic beta-antagonists are used for treatment of hypertension, cardiac arrhythmias, angina pectoris, glaucoma, migraine headaches, and anxiety. [e]
- Adrenergic uptake inhibitor [r]: Drug which acts as a reuptake inhibitor for the neurotransmitters norepinephrine and epinephrine by blocking the action of the norepinephrine transporter. [e]
- Beta-2 adrenergic receptor [r]: Cell surface receptors of the G-protein-coupled receptor type that are in the sympathetic nervous system. [e]
- G-protein-coupled receptor kinase [r]: A family of protein kinases which regulate the activity of G protein-coupled receptors (GPCRs) by phosphorylating their intracellular domains after their associated G proteins have been released and activated. [e]