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The basal forebrain (BF) is a complex structure that plays key roles in regulating various brain functions. However, it remains unclear how cholinergic and non-cholinergic BF neurons modulate large-scale functional networks and their relevance in intrinsic and extrinsic behaviors. With an optimized awake mouse optogenetic fMRI approach, we revealed that optogenetic stimulation of four BF neuron types evoked distinct cell-type-specific whole-brain BOLD activations, which could be attributed to BF-originated low-dimensional structural networks. Additionally, optogenetic activation of VGLUT2, ChAT, and PV neurons in the BF modulated the preference for locomotion, exploration, and grooming, respectively. Furthermore, we uncovered the functional network basis of the above BF-modulated behavioral preference through a decoding model linking the BF-modulated BOLD activation, low-dimensional structural networks, and behavioral preference. To summarize, we decoded the functional network basis of differential behavioral preferences with cell-type-specific optogenetic fMRI on the BF and provided an avenue for investigating mouse behaviors from a whole-brain view.
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http://dx.doi.org/10.1016/j.neuron.2024.01.017 | DOI Listing |
Nat Methods
September 2025
Department of Radiology, Michigan State University, East Lansing, MI, USA.
Concurrent recording of electroencephalogram (EEG) and functional magnetic resonance imaging (fMRI) signals reveals cross-scale neurovascular dynamics crucial for explaining fundamental linkages between function and behaviors. However, MRI scanners generate artifacts for EEG detection. Despite existing denoising methods, cabled connections to EEG receivers are susceptible to environmental fluctuations inside MRI scanners, creating baseline drifts that complicate EEG signal retrieval from the noisy background.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
August 2025
Center for Neuroscience Imaging Research, Institute for Basic Science, Suwon 16419, Republic of Korea.
Functional connectivity (FC), a statistical correlation of pair-wise brain signals from resting-state (RS) functional MRI (fMRI), is a widely used concept for mapping large-scale functional networks in both humans and animals. However, its underlying causal mechanism remains poorly understood, particularly for strong interhemispheric connectivity (e.g.
View Article and Find Full Text PDFImaging Neurosci (Camb)
October 2024
Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA, United States.
Whole-brain intrinsic activity as detected by resting-state fMRI can besummarized by three primary spatiotemporal patterns. These patterns have beenshown to change with different brain states, especially arousal. Thenoradrenergic locus coeruleus (LC) is a key node in arousal circuits and hasextensive projections throughout the brain, giving it neuromodulatory influenceover the coordinated activity of structurally separated regions.
View Article and Find Full Text PDFAdv Sci (Weinh)
July 2025
Key Laboratory of Mental Health of the Ministry of Education, Guangdong-Hong Kong-Macao, Greater Bay Area Center for Brain Science and Brain-Inspired Intelligence, Guangdong-Hong Kong Joint Laboratory for Psychiatric Disorders, Guangdong Province Key Laboratory of Psychiatric Disorders, Guangdong Ba
Cortical traveling waves coordinate communication among distributed neural ensembles to modulate brain function and dysfunction through distinct spatiotemporal propagation patterns. However, the brain-wide propagation dynamics of traveling waves from different origins and their roles in regulating behavior remain unclear. Using optogenetics alongside whole-brain fMRI in mice, it is demonstrated that optogenetic activation of the medial prefrontal cortex and primary somatosensory area induces cortical spreading depression (CSD)-like traveling waves.
View Article and Find Full Text PDFNat Commun
July 2025
Center for Neuroscience Imaging Research (CNIR), Institute for Basic Science (IBS), Suwon, Republic of Korea.
Somatostatin-expressing (SST) interneurons modulate hemodynamic responses both directly and indirectly, but their precise role remains unclear. Here, we investigated the influence of SST interneurons on hemodynamic control in response to optogenetic stimulation of SST neurons and somatosensory stimulation in both awake and anesthetized mice. Prolonged optogenetic stimulation of SST neurons induces fast vasodilation through nitric oxide synthase-expressing neurons that co-express SST, and slow vasodilation mediated by astrocytes.
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