上腺素通过星纯能信号改变行为状态
Alex B Chen1,2,3, Marc Duque2,3, Altyn Rymbek4
1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
概括
上腺素 (NE) 激发星球细胞释放ATP,而ATP变成腺素,抑制行为. 这揭示了星纯能信号在NE介导的大脑状态转换中的关键作用.
科学领域:
- 神经科学
- 细胞信号传输
- 行为生物学
背景情况:
- 神经元和质细胞通过神经调节器进行通信,但它们在电路计算和行为中的交互作用在很大程度上是未知的.
- 上腺素 (NE) 是一种神经调节剂,影响行为和神经活动,调解快速激发和延迟抑制.
研究的目的:
- 研究神经元-质相互作用的机制,特别是涉及神经调节器,影响电路计算和行为.
- 阐明星纯能信号在行为转变期间中介于上腺素 (NE) 的抑制作用.
主要方法:
- 使用幼虫斑马鱼作为模型系统来研究无用性诱导的行为转变.
- 研究了涉及上腺素 (NE),星,纯能信号 (ATP,腺) 和神经腺受体的信号通路.
主要成果:
- 证明星纯能信号介导NE驱动的行为和电路活动变化的抑制成分.
- 显示NE刺激基三酸盐 (ATP) 的释放,而基三酸盐在细胞外转化为基酸.
- 证实腺会激活脑后的神经腺受体,导致行为抑制.
结论:
- 在行为和大脑状态转换过程中,星纯能信号是北上腺素 (NE) 介导的抑制动机的关键组成部分.
- 这项研究强调了星质作为神经调节信号的作用,影响复杂的行为.
- 这些发现将星体定位为NE驱动的行为调节和大脑状态调节的关键参与者.
相关概念视频
Adrenergic Neurons: Neurotransmission
3.3K
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.
Synthesis: Catecholamine synthesis requires tyrosine, which...
Synthesis: Catecholamine synthesis requires tyrosine, which...
3.3K
Sympathetic Signaling
813
Sympathetic signaling, a vital part of the autonomic nervous system, plays a crucial role in mobilizing the body's resources in response to stress or emergencies. It involves the transmission of nerve impulses from sympathetic preganglionic fibers to postganglionic fibers. This results in the release of specific neurotransmitters and activation of adrenergic receptors.
Sympathetic preganglionic fibers release the neurotransmitter acetylcholine (ACh) onto the ganglionic neurons in the...
Sympathetic preganglionic fibers release the neurotransmitter acetylcholine (ACh) onto the ganglionic neurons in the...
813
Drugs Affecting Neurotransmitter Release or Uptake
914
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...
914
Adrenergic Receptors: β Subtype
1.5K
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...
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...
1.5K
GPCRs Regulate Adenylyl Cylase Activity
5.1K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.1K
Adrenergic Receptors (Adrenoceptors): Classification
2.2K
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,...
α-Adrenoceptors
α-Adrenoceptors are classified into two main subtypes: α1 and α2. The α1 adrenoceptors,...
2.2K


