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内源性大麻素通过刺激星形胶质细胞增强突触传递。

Endocannabinoids potentiate synaptic transmission through stimulation of astrocytes.

机构信息

Instituto Cajal, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

出版信息

Neuron. 2010 Oct 6;68(1):113-26. doi: 10.1016/j.neuron.2010.08.043.

Abstract

Endocannabinoids and their receptor CB1 play key roles in brain function. Astrocytes express CB1Rs that are activated by endocannabinoids released by neurons. However, the consequences of the endocannabinoid-mediated neuron-astrocyte signaling on synaptic transmission are unknown. We show that endocannabinoids released by hippocampal pyramidal neurons increase the probability of transmitter release at CA3-CA1 synapses. This synaptic potentiation is due to CB1R-induced Ca(2+) elevations in astrocytes, which stimulate the release of glutamate that activates presynaptic metabotropic glutamate receptors. While endocannabinoids induce synaptic depression in the stimulated neuron by direct activation of presynaptic CB1Rs, they indirectly lead to synaptic potentiation in relatively more distant neurons by activation of CB1Rs in astrocytes. Hence, astrocyte calcium signal evoked by endogenous stimuli (neuron-released endocannabinoids) modulates synaptic transmission. Therefore, astrocytes respond to endocannabinoids that then potentiate synaptic transmission, indicating that astrocytes are actively involved in brain physiology.

摘要

内源性大麻素及其受体 CB1 在大脑功能中发挥着关键作用。星形胶质细胞表达 CB1R,可被神经元释放的内源性大麻素激活。然而,内源性大麻素介导的神经元-星形胶质细胞信号对突触传递的影响尚不清楚。我们发现,海马锥体神经元释放的内源性大麻素增加了 CA3-CA1 突触递质释放的概率。这种突触增强是由于 CB1R 诱导星形胶质细胞内 Ca2+ 升高,刺激谷氨酸释放,从而激活突触前代谢型谷氨酸受体。虽然内源性大麻素通过直接激活突触前 CB1R 诱导刺激神经元中的突触抑制,但它们通过激活星形胶质细胞中的 CB1R 间接地导致相对更远的神经元中的突触增强。因此,内源性刺激(神经元释放的内源性大麻素)引发的星形胶质细胞钙信号调节突触传递。因此,星形胶质细胞对内源性大麻素做出反应,进而增强突触传递,这表明星形胶质细胞积极参与脑生理学。

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