カテコロアミンの吸収は,副腎中枢の粒子分泌によって行われます
まとめ
牛の副腎髄クロマフィン粒子は,カタチョラミンを積極的に輸送する. マグネシウムとATPは,この吸収を著しく強化し,レザーピンとEDTAによって抑制されます.
科学分野:
- バイオケミストリー バイオケミストリー
- 細胞生物学 細胞生物学
- 神経科学は神経科学である.
背景:
- クロマフィン粒子は,副腎髄におけるカテキオラミンの鍵となる貯蔵ベジクルである.
- カテキオラミン輸送の理解は,神経内分泌研究にとって極めて重要です.
研究 の 目的:
- 孤立したクロマフィン粒子がカテキオラミンを吸収するメカニズムを調査する.
- これらの膀におけるカテキオラミン輸送に影響を与える要因を特定する.
主な方法:
- 牛の副腎髄からクロマフィン粒子を分離する.
- 異なる温度 (0°C vs. 37°C) でC(14) ラベル付きカテキオラミンの摂取量を測定する.
- Mg ((++),アデノシン・トリフォスファート (ATP),レザーピン,エチレン・ダイアミネ・テトラエセチック酸 (EDTA) の摂取に対する影響の評価.
主要な成果:
- カテコロアミンの吸収は,0°Cと比較して37°Cで有意に増加し,活発なプロセスを示した.
- 吸収はMg (((++)) とATPによって3〜5倍に刺激されました.
- レザーピン (1 x 10(-5) M) は90%の吸収を阻害しました.
- EDTAはMgとATP刺激による吸収を完全に阻害しましたが,過剰なMgとMgとでこの阻害は逆転することができました.
結論:
- クロマフィン粒子は,カテキオラミンの活性輸送システムを備えています.
- この輸送システムは,Mg ((++) とATPに依存しています.
- この発見は,Mg ((++) に依存するATPアゼが,クロマフィン粒子のカテキオラミンの吸収に関与していることを示唆している.
キーワード:
副腎髄/代謝について関連する概念動画
Adrenergic Neurons: Neurotransmission
Postganglionic sympathetic fibers (except those supplying the sweat glands) releasing noradrenaline or norepinephrine are called noradrenergic or adrenergic neurons. Noradrenaline, dopamine, adrenaline, or epinephrine are collectively called "catecholamines" as they contain a catechol moiety and an amine side chain. The five stages of neurotransmitter release involve their synthesis, storage, release, reuptake and metabolism.
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Synthesis: Catecholamine synthesis requires tyrosine, which is taken...
Adrenergic Receptors (Adrenoceptors): Classification
Adrenergic receptors, or adrenoceptors, respond to the autonomic neurotransmitter noradrenaline and other endogenous catecholamine agonists. They are classified into two main families, α and β, based on their pharmacological response and are further subdivided depending on their location, elicited response, and affinity to specific agonists or antagonists.
α-Adrenoceptors
α-Adrenoceptors are classified into two main subtypes: α1 and α2. The α1 adrenoceptors, which are found on postsynaptic...
α-Adrenoceptors
α-Adrenoceptors are classified into two main subtypes: α1 and α2. The α1 adrenoceptors, which are found on postsynaptic...
Adrenergic Receptors: ɑ Subtype
Adrenoceptors are classified into α and ꞵ classes based on their potencies to catecholamine agonists. α-adrenoceptors show the following order of catecholamine potency:
Adrenaline ≥ Noradrenaline >> Isoprenaline
α-adrenoceptors are further divided into α1 and α2-adrenoceptors.
α1-Adrenoceptors: These receptors are located postsynaptically on the effector organs and cause constriction of smooth muscle mediated by activation of phospholipase C—inositol-1,4,5-trisphosphate...
Adrenaline ≥ Noradrenaline >> Isoprenaline
α-adrenoceptors are further divided into α1 and α2-adrenoceptors.
α1-Adrenoceptors: These receptors are located postsynaptically on the effector organs and cause constriction of smooth muscle mediated by activation of phospholipase C—inositol-1,4,5-trisphosphate...
Adrenergic Receptors: β Subtype
β-adrenoceptors have varied sensitivities towards adrenaline, noradrenaline, and isoprenaline. The order of agonist potency is as follows:
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors have equal affinities for...
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors have equal affinities for...
Adrenergic Agonists: Indirect-Acting Agents
Indirect-acting adrenergic agonists potentiate the effects of endogenous catecholamines through different mechanisms without directly binding to adrenoceptors.
One mechanism involves depleting stored catecholamines by displacing them from synaptic vesicles. These agents, known as "displacers," are transported into vesicles at the expense of noradrenaline. Examples include amphetamine and tyramine, which lack a catechol moiety, resulting in prolonged action, improved oral bioavailability, and...
One mechanism involves depleting stored catecholamines by displacing them from synaptic vesicles. These agents, known as "displacers," are transported into vesicles at the expense of noradrenaline. Examples include amphetamine and tyramine, which lack a catechol moiety, resulting in prolonged action, improved oral bioavailability, and...
Drugs Affecting Neurotransmitter Release or Uptake
Certain drugs can affect how neurotransmitters called catecholamines, are released or taken back up in the adrenergic neuron. They can have different effects on the body's sympathetic transmission. Reserpine, a natural compound found in the Rauwolfia shrub, blocks a transporter called vesicular monoamine transporter (VMAT), which leads to a buildup of catecholamines in the cell and reduces sympathetic transmission. Another drug called guanethidine works in multiple ways, including blocking...


