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体内神经活动生理和病理时间尺度上的内源性大麻素动态。

In vivo endocannabinoid dynamics at the timescale of physiological and pathological neural activity.

机构信息

Department of Neurosurgery, Stanford University, Stanford, CA 94305, USA; Hotchkiss Brain Institute, University of Calgary, Calgary, AB T2N 4N1, Canada; Department of Anatomy and Cell Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.

Hotchkiss Brain Institute, University of Calgary, Calgary, AB T2N 4N1, Canada; Department of Anatomy and Cell Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.

出版信息

Neuron. 2021 Aug 4;109(15):2398-2403.e4. doi: 10.1016/j.neuron.2021.05.026.

Abstract

The brain's endocannabinoid system is a powerful controller of neurotransmitter release, shaping synaptic communication under physiological and pathological conditions. However, our understanding of endocannabinoid signaling in vivo is limited by the inability to measure their changes at timescales commensurate with the high lability of lipid signals, leaving fundamental questions of whether, how, and which endocannabinoids fluctuate with neural activity unresolved. Using novel imaging approaches in awake behaving mice, we now demonstrate that the endocannabinoid 2-arachidonoylglycerol, not anandamide, is dynamically coupled to hippocampal neural activity with high spatiotemporal specificity. Furthermore, we show that seizures amplify the physiological endocannabinoid increase by orders of magnitude and drive the downstream synthesis of vasoactive prostaglandins that culminate in a prolonged stroke-like event. These results shed new light on normal and pathological endocannabinoid signaling in vivo.

摘要

大脑的内源性大麻素系统是神经递质释放的强大控制器,在生理和病理条件下塑造突触通讯。然而,我们对内源性大麻素信号在体内的理解受到限制,因为无法在与脂质信号高不稳定性相称的时间尺度上测量它们的变化,这使得关于内源性大麻素是否以及如何随神经活动波动的基本问题仍未解决。使用在清醒活动的小鼠中新型的成像方法,我们现在证明内源性大麻素 2-花生四烯酰甘油而不是花生四烯酸酰胺,与海马体神经活动具有高度时空特异性的动态偶联。此外,我们还表明,癫痫发作使生理内源性大麻素增加了数量级,并驱动血管活性前列腺素的下游合成,最终导致长时间的类似中风的事件。这些结果为体内正常和病理内源性大麻素信号提供了新的认识。

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