分子认知实验室Molecular Cognition Lab 研究GABA抑制性突触的发育、调控与疾病机制Development, modulation, and disease mechanisms of GABAergic inhibitory synapses
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聚 jù · assemble
突触组装 Synapse Assembly

GABA-A受体与Shisa7、TMEM132B等辅助亚基如何聚集、组装成功能性抑制性突触。 How GABA-A receptors and auxiliary subunits such as Shisa7 and TMEM132B cluster and assemble into functional inhibitory synapses.

聚 — synapse assembly illustration
散 sàn · disperse
突触外信号与张力性抑制 Extrasynaptic Signaling & Tonic Inhibition

弥散于突触外膜的受体介导持续的“张力性抑制”——大脑的背景刹车;受体的扩散与转运动态调节这一过程。 Receptors dispersed across the extrasynaptic membrane mediate persistent "tonic" inhibition — the brain's background brake — dynamically tuned by receptor diffusion and trafficking.

散 — extrasynaptic tonic inhibition illustration
转 zhuǎn · transform
状态转换 State Transitions

睡眠与觉醒如何动态调控抑制性突触可塑性;麻醉与意识转换的分子与神经环路机制。 How sleep and wakefulness dynamically regulate inhibitory synaptic plasticity; the molecular and circuit mechanisms of anesthesia and consciousness.

转 — brain state transition illustration
调 tiáo · modulate
变构调节 Allosteric Modulation

苯二氮䓬类药物、酒精与麻醉剂如何变构调节GABA-A受体——下一代神经系统疾病药物的靶点。 How benzodiazepines, alcohol, and anesthetics allosterically modulate GABA-A receptors — targets for next-generation therapeutics for brain disorders.

调 — allosteric modulation illustration

陆伟实验室(分子认知实验室)· 深圳医学科学院神经调控与认知研究所 · 深圳市光明区卫光生命科学园区 Lu Lab (Molecular Cognition Lab) · Institute of Neuromodulation and Cognition, SMART · Weiguang Life Science Park, Guangming District, Shenzhen

luwei@smart.org.cn · gaba@smart.org.cn · © 2025–2026 Lu Lab