Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice.
Arousal state transitions occlude sensory-evoked neurovascular coupling in neonatal mice.
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DOI:
10.1038/s42003-023-05121-5
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发表时间:
2023-07-17
影响因子:
5.9
通讯作者:
Drew, Patrick J. J.
中科院分区:
文献类型:
--
作者:
Gheres, Kyle W. W.;Unsal, Hayreddin S. S.;Han, Xu;Zhang, Qingguang;Turner, Kevin L. L.;Zhang, Nanyin;Drew, Patrick J. J.
In the adult sensory cortex, increases in neural activity elicited by sensory stimulation usually drive vasodilation mediated by neurovascular coupling. However, whether neurovascular coupling is the same in neonatal animals as adults is controversial, as both canonical and inverted responses have been observed. We investigated the nature of neurovascular coupling in unanesthetized neonatal mice using optical imaging, electrophysiology, and BOLD fMRI. We find in neonatal (postnatal day 15, P15) mice, sensory stimulation induces a small increase in blood volume/BOLD signal, often followed by a large decrease in blood volume. An examination of arousal state of the mice revealed that neonatal mice were asleep a substantial fraction of the time, and that stimulation caused the animal to awaken. As cortical blood volume is much higher during REM and NREM sleep than the awake state, awakening occludes any sensory-evoked neurovascular coupling. When neonatal mice are stimulated during an awake period, they showed relatively normal (but slowed) neurovascular coupling, showing that that the typically observed constriction is due to arousal state changes. These result show that sleep-related vascular changes dominate over any sensory-evoked changes, and hemodynamic measures need to be considered in the context of arousal state changes. A combination of optical imaging, electrophysiology, and BOLD fMRI in unanesthetized neonatal mice reveals that sleep-related vascular changes dominate over sensory-evoked changes.
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DOI:
10.1177/1073858418805427
发表时间:
2019-08
期刊:
The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry
影响因子:
--
作者:
Drew PJ;Winder AT;Zhang Q
通讯作者:
Zhang Q
影响因子:
2.7
作者:
Arakawa, Hiroyuki;Erzurumlu, Reha S.
通讯作者:
Erzurumlu, Reha S.
影响因子:
4.6
作者:
Adams MD;Winder AT;Blinder P;Drew PJ
通讯作者:
Drew PJ
影响因子:
48
作者:
Drew, Patrick J.;Shih, Andy Y.;Driscoll, Jonathan D.;Knutsen, Per Magne;Blinder, Pablo;Davalos, Dimitrios;Akassoglou, Katerina;Tsai, Philbert S.;Kleinfeld, David
通讯作者:
Kleinfeld, David
影响因子:
6.3
作者:
Bekar, Lane K.;Wei, Helen S.;Nedergaard, Maiken
通讯作者:
Nedergaard, Maiken