Myogenic mechanism: Difference between revisions
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== Myogenic Mechanism == | |||
[[File:Bayliss_effect.png|thumb|right|Illustration of the Bayliss effect, a key component of the myogenic mechanism.]] | |||
The myogenic mechanism is | The '''myogenic mechanism''' is an intrinsic property of vascular smooth muscle that enables blood vessels to respond to changes in pressure. This mechanism is crucial for the regulation of blood flow and blood pressure within the body, particularly in the [[kidney]]s and [[brain]]. | ||
== | === Overview === | ||
The myogenic mechanism is a type of [[autoregulation]] that occurs in the [[arteriole]]s, the small branches of [[artery|arteries]]. When the pressure within a blood vessel increases, the vessel wall is stretched. This stretch is detected by the smooth muscle cells in the vessel wall, which respond by contracting. This contraction reduces the diameter of the vessel, thereby increasing the resistance to blood flow and maintaining a relatively constant flow despite the increased pressure. | |||
Conversely, when the pressure decreases, the smooth muscle cells relax, allowing the vessel to dilate and decrease resistance, thus maintaining blood flow. This response is known as the [[Bayliss effect]], named after Sir William Bayliss, who first described it in 1902. | |||
== | === Mechanism === | ||
The myogenic response is initiated by the stretch of the vascular smooth muscle cells. This stretch activates mechanosensitive ion channels in the cell membrane, leading to an influx of [[calcium]] ions. The increase in intracellular calcium concentration triggers the contraction of the smooth muscle cells. | |||
The contraction of the smooth muscle cells is mediated by the interaction of calcium with the protein [[calmodulin]], which activates [[myosin light-chain kinase]] (MLCK). MLCK phosphorylates the myosin light chains, enabling the interaction of myosin with [[actin]] filaments, resulting in muscle contraction. | |||
== | === Physiological Importance === | ||
The myogenic mechanism plays a vital role in maintaining stable blood flow to organs that require constant perfusion, such as the brain and kidneys. In the [[cerebral circulation]], it helps protect the brain from damage due to fluctuations in blood pressure. In the [[renal circulation]], it contributes to the regulation of [[glomerular filtration rate]] (GFR) by maintaining stable blood flow through the [[glomerulus]]. | |||
=== Clinical Relevance === | |||
Dysfunction of the myogenic mechanism can lead to various pathological conditions. For example, impaired myogenic response in the cerebral circulation can contribute to [[stroke]] or [[cerebral edema]]. In the kidneys, it can affect the regulation of blood pressure and contribute to [[hypertension]]. | |||
== Related Pages == | |||
* [[Autoregulation]] | * [[Autoregulation]] | ||
* [[Vascular smooth muscle]] | * [[Vascular smooth muscle]] | ||
* [[Cerebral circulation]] | |||
* [[Renal circulation]] | * [[Renal circulation]] | ||
* [[ | * [[Hypertension]] | ||
[[Category:Physiology]] | [[Category:Physiology]] | ||
[[Category:Cardiovascular system]] | [[Category:Cardiovascular system]] | ||
Latest revision as of 11:34, 15 February 2025
Myogenic Mechanism[edit]

The myogenic mechanism is an intrinsic property of vascular smooth muscle that enables blood vessels to respond to changes in pressure. This mechanism is crucial for the regulation of blood flow and blood pressure within the body, particularly in the kidneys and brain.
Overview[edit]
The myogenic mechanism is a type of autoregulation that occurs in the arterioles, the small branches of arteries. When the pressure within a blood vessel increases, the vessel wall is stretched. This stretch is detected by the smooth muscle cells in the vessel wall, which respond by contracting. This contraction reduces the diameter of the vessel, thereby increasing the resistance to blood flow and maintaining a relatively constant flow despite the increased pressure.
Conversely, when the pressure decreases, the smooth muscle cells relax, allowing the vessel to dilate and decrease resistance, thus maintaining blood flow. This response is known as the Bayliss effect, named after Sir William Bayliss, who first described it in 1902.
Mechanism[edit]
The myogenic response is initiated by the stretch of the vascular smooth muscle cells. This stretch activates mechanosensitive ion channels in the cell membrane, leading to an influx of calcium ions. The increase in intracellular calcium concentration triggers the contraction of the smooth muscle cells.
The contraction of the smooth muscle cells is mediated by the interaction of calcium with the protein calmodulin, which activates myosin light-chain kinase (MLCK). MLCK phosphorylates the myosin light chains, enabling the interaction of myosin with actin filaments, resulting in muscle contraction.
Physiological Importance[edit]
The myogenic mechanism plays a vital role in maintaining stable blood flow to organs that require constant perfusion, such as the brain and kidneys. In the cerebral circulation, it helps protect the brain from damage due to fluctuations in blood pressure. In the renal circulation, it contributes to the regulation of glomerular filtration rate (GFR) by maintaining stable blood flow through the glomerulus.
Clinical Relevance[edit]
Dysfunction of the myogenic mechanism can lead to various pathological conditions. For example, impaired myogenic response in the cerebral circulation can contribute to stroke or cerebral edema. In the kidneys, it can affect the regulation of blood pressure and contribute to hypertension.