6-尼特罗多巴胺是子体洞穴松放松的内源调解剂
Antonio Tiago Lima1, José Britto-Júnior1, Manoel Odorico Moraes2
1Faculty of Medical Sciences, Department of Pharmacology, University of Campinas (UNICAMP), Campinas, Brazil.
Andrology
|December 29, 2023
概括
6-尼特罗多巴胺 (6-ND) 是体洞膜平滑肌的强效内源性放松剂,通过多巴胺D2受体起作用. 它的非神经性释放和对多巴胺诱导的收缩的抑制作用表明它在调节光滑肌肉度方面发挥着关键作用.
科学领域:
- 药理学 药理学是指药理学的学科.
- 泌尿器科 泌尿器科 泌尿器科 泌尿器科
- 生理学 生理学 生理学
背景情况:
- 6-尼特罗多巴胺 (6-ND) 是一种具有已知的血管光滑肌肉松性质的内源性甲醇胺.
- 它在洞穴体 (CC) 中的作用和释放机制在很大程度上仍未被探索.
研究的目的:
- 为了研究从体洞穴体 (RbCC) 基底释放的6-ND和诺亚上腺素.
- 描述6-ND对RbCC的放松作用及其潜在的作用机制.
主要方法:
- 对RbCC的剖析和器官浴室研究.
- 使用液体染色学-并联质谱法量化6-ND和诺亚丁上腺素释放的量化.
- 对6 - ND在内甲林-1预先合并的RbCC条上放松活性的评估.
主要成果:
- RbCC表现出基底释放的6-ND和诺亚上腺素.
- 6-ND的释放是非神经性,不同于诺亚上腺素,并通过氧化物合成抑制调节.
- 6-ND和选择性多巴胺D2激动剂诱导了依赖度的放松,而6-ND作为一种强大的多巴胺D2受体对抗剂.
结论:
- 6-尼特罗多巴胺是迄今为止在RbCC中发现的最强大的内源性放松剂.
- 它代表了一种新的氧化介导的途径,用于CC平滑肌肉放松.
- 多巴胺和6-ND之间的平衡在体内调节CC光滑肌肉度方面可能至关重要.
相关概念视频
Nitric Oxide Signaling Pathway
5.0K
Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure...
5.0K
Antihypertensive Drugs: Vasodilators
528
Vasodilators, primarily affecting the smooth muscles within arterial and venous walls, are commonly used for hypertension treatment. Medications such as minoxidil and hydralazine primarily target arteries and arterioles, while sodium nitroprusside acts on arterioles and venules. Minoxidil, functioning as a prodrug, is metabolized by hepatic sulfotransferase into its active form, minoxidil sulfate, after oral administration. This metabolite binds to the sulfonylurea receptor (SUR) component of...
528
Male Sexual Response: Erection & Ejaculation
2.4K
Sexual stimulation can take various forms, such as physical touch and visual or auditory cues. When this happens, the parasympathetic reflex in the sacral portion of the spinal cord is activated. This reflex stimulates the release of nitric oxide (NO), which then dilates the arterioles in the penis, increasing blood flow to the erectile tissues - the corpora cavernosa and corpus spongiosum.
The blood filling the erectile tissues compresses the veins, which helps to prevent blood from leaving...
The blood filling the erectile tissues compresses the veins, which helps to prevent blood from leaving...
2.4K
Adrenergic Agonists: Indirect-Acting Agents
1.6K
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...
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...
1.6K
Direct-Acting Cholinergic Agonists: Pharmacological Actions
1.3K
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...
1.3K
Drugs Affecting Neurotransmitter Synthesis
1.4K
Drugs affecting neurotransmitter synthesis can impact the adrenergic neuron and the synthesis of neurotransmitters. For example, α-methyltyrosine and carbidopa target specific enzymes involved in catecholamine synthesis. α-methyltyrosine inhibits the enzyme tyrosine hydroxylase, which converts tyrosine into dopamine. By blocking this enzyme, α-methyltyrosine reduces dopamine production and other catecholamines. Carbidopa, on the other hand, inhibits the enzyme dopa decarboxylase,...
1.4K


