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Chao, T.-H.

Publications and source records attributed to Chao, T.-H..

2 recordsLinked to original sources

Single-shot simultaneous BOLD and velocity-encoding MRI for functional and slow-flow imaging

Cerebrospinal fluid (CSF) motion is coupled with global blood oxygenation level-dependent (BOLD) fluctuations, but the spatial relationship between regional brain activity and CSF dynamics remains poorly understood. Here, we developed a single-shot BOLD-VENC sequence that combines gradient-echo BOLD imaging with spin-echo velocity encoding following the same RF excitation, enabling simultaneous measurement of brain-wide BOLD activity and spatially resolved slow CSF velocity at 3T. The velocity measurement was validated in a slow-flow phantom and in five healthy participants using paced-breathing, breath-holding, and visual-stimulation experiments. Phantom measurements showed strong agreement with prescribed velocities over 0.1-1.0 mm/s (R2 = 0.93-0.98). In vivo measurements demonstrated respiratory- and cardiac-dependent changes in CSF velocity magnitude and direction across the ventricles and cortical subarachnoid spaces (SAS). The established coupling between the negative derivative of the global BOLD signal and fourth-ventricle CSF inflow was reproduced, with a peak lag of 0.9 s. Global BOLD fluctuations were also coupled with spatially distributed CSF velocity changes across ventricular and cortical CSF spaces, with a similar peak lag of 1.2 s. During visual checkerboard stimulation, BOLD-CSF velocity coupling was localized primarily to the SAS surrounding the activated visual cortex, demonstrating a regional relationship between local BOLD activity and nearby CSF motion. These findings establish the feasibility of simultaneous BOLD and slow CSF velocity imaging and extend BOLD-CSF coupling from a global measure toward spatially resolved assessment of hemodynamic-CSF interactions.

neuroscience↗

Acute and chronic alcohol modulation of extended amygdala calcium dynamics

The central amygdala (CeA) and bed nucleus of the stria terminalis (BNST) are reciprocally connected nodes of the extended amygdala thought to play an important role in alcohol consumption. Studies of immediate-early genes indicate that BNST and CeA are acutely activated following alcohol drinking and may signal alcohol reward in nondependent drinkers, while increased stress signaling in the extended amygdala following chronic alcohol exposure drives increased drinking via negative reinforcement. However, the temporal dynamics of neuronal activation in these regions during drinking behavior are poorly understood. In this study, we used fiber photometry and the genetically encoded calcium sensor GCaMP6s to assess acute changes in neuronal activity during alcohol consumption in BNST and CeA before and after a chronic drinking paradigm. Activity was examined in the pan-neuronal population and separately in dynorphinergic neurons. BNST and CeA showed increased pan-neuronal activity during acute consumption of alcohol and other fluid tastants of positive and negative valence, as well as highly palatable chow. Responses were greatest during initial consummatory bouts and decreased in amplitude with repeated consumption of the same tastant, suggesting modulation by stimulus novelty. Dynorphin neurons showed similar consumption-associated calcium increases in both regions. Following three weeks of continuous alcohol access (CA), calcium increases in dynorphin neurons during drinking were maintained, but pan-neuronal activity and BNST-CeA coherence were altered in a sex-specific manner. These results indicate that BNST and CeA, and dynorphin neurons specifically, are engaged during drinking behavior, and activity dynamics are influenced by stimulus novelty and chronic alcohol.

neuroscience↗