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5.9: Direct-Acting Cholinergic Agonists: Pharmacological Actions

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Pharmacology

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Direct-Acting Cholinergic Agonists: Pharmacological Actions
 
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5.9: Direct-Acting Cholinergic Agonists: Pharmacological Actions

Direct-acting cholinergic agonists exert their pharmacological actions by mimicking the effects of acetylcholine on postsynaptic muscarinic receptors to generate parasympathetic responses. These agents elicit a range of physiological responses, including cardiovascular effects. For example, activation of muscarinic receptors induces bradycardia, decreased cardiac output, reduced peripheral resistance, and consequent hypotension. In the eye, stimulation of M3 receptors leads to smooth muscle contraction in the iris, resulting in miosis. Simultaneously, the contraction of the ciliary muscle adjusts the lens curvature and focal length, improving near vision. These actions help regulate aqueous humor outflow and intraocular pressure, making them beneficial in treating glaucoma.

Furthermore, muscarinic agonists induce smooth muscle contractions in the urinary and respiratory systems while enhancing peristalsis in the gastrointestinal tract. Synthetic direct-acting agents capable of crossing the blood-brain barrier elicit central nervous system effects, including cortical stimulation, tremor, and hypothermia. Nicotinic agonists activate receptors at neuromuscular junctions, leading to depolarization, increased ion permeability, and subsequent muscle contraction.

Knowledge of the uses and side effects of cholinergic agonists is crucial in managing the various physiological processes for which they are prescribed.

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Keywords: Direct-acting Cholinergic Agonists Muscarinic Receptors Parasympathetic Responses Cardiovascular Effects Bradycardia Decreased Cardiac Output Peripheral Resistance Hypotension Miosis Ciliary Muscle Aqueous Humor Intraocular Pressure Glaucoma Smooth Muscle Contraction Urinary System Respiratory System Gastrointestinal Tract Peristalsis Central Nervous System Cortical Stimulation Tremor Hypothermia Nicotinic Agonists Neuromuscular Junctions Muscle Contraction

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