The overall objective of this research project is to elucidate the roles of specific basal forebrain (BF) neuronal populations as potential neural mechanisms for attention. Specifically, we seek to determine how attention-related cortical activity is dynamically shaped by BF inputs. Substantial effort during the current reporting period has focused predominantly on start-up activities, including lab set up, staff recruitment and training, animal acquisition and the development of behavioral paradigms. As a first step toward establishing rodent behavioral tasks that capture behavioral and electrophysiological signatures of attention tasks used in human studies, we have adopted the commonly used oddball procedure in human attention studies in the rat rats were presented with a stream of frequent standard tones (90%, 10kHz) and infrequent target tones (10%, 6kHz) once every second. Response to the target, but not to the standard, results in reward delivery. We are characterizing the neurophysiological responses in order to validate this paradigm as a model of human ERP responses. In a separate collaborative study with Dr. Hao Zhang and Dr. Miguel Nicolelis at Duke University, we investigated the real-time in vivo dynamic interaction between acetylcholine release originating from the medial septum, the anterior extension of the BF, and the neurophysiological activity (theta oscillation) in the hippocampus. By implementing simultaneous amperometric and electrophysiological recordings in urethane-anesthetized rats, we established that the phasic in vivo acetylcholine release is tightly coupled with hippocampal theta oscillation, on spatiotemporal scales (over tens of seconds and within 0.3mm depth) much finer than previously known. Moreover, we found that the phasic acetylecholine signal lagged behind the onset of theta oscillation by 25-60 seconds, suggesting that acetyocholine modulation may not be required for the initiation of theta oscillations. Instead, our findings suggest that acetylcholine signals may be recruited after sustained theta oscillation, to operate synergistically with theta oscillations in order to promote plasticity in the hippocampus.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Investigator-Initiated Intramural Research Projects (ZIA)
Project #
1ZIAAG000339-01
Application #
8156773
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2010
Total Cost
$370,806
Indirect Cost
Name
National Institute on Aging
Department
Type
DUNS #
City
State
Country
Zip Code
Whitmore, Nathan W; Lin, Shih-Chieh (2016) Unmasking local activity within local field potentials (LFPs) by removing distal electrical signals using independent component analysis. Neuroimage 132:79-92
Raver, Sylvina M; Lin, Shih-Chieh (2015) Basal forebrain motivational salience signal enhances cortical processing and decision speed. Front Behav Neurosci 9:277
Mayse, Jeffrey D; Nelson, Geoffrey M; Avila, Irene et al. (2015) Basal forebrain neuronal inhibition enables rapid behavioral stopping. Nat Neurosci 18:1501-8
Nguyen, David P; Lin, Shih-Chieh (2014) A frontal cortex event-related potential driven by the basal forebrain. Elife 3:e02148
Avila, Irene; Lin, Shih-Chieh (2014) Distinct neuronal populations in the basal forebrain encode motivational salience and movement. Front Behav Neurosci 8:421
Avila, Irene; Lin, Shih-Chieh (2014) Motivational salience signal in the basal forebrain is coupled with faster and more precise decision speed. PLoS Biol 12:e1001811
Mayse, Jeffrey D; Nelson, Geoffrey M; Park, Pul et al. (2014) Proactive and reactive inhibitory control in rats. Front Neurosci 8:104
Zhang, Hao; Lin, Shih-Chieh; Nicolelis, Miguel A L (2011) A distinctive subpopulation of medial septal slow-firing neurons promote hippocampal activation and theta oscillations. J Neurophysiol 106:2749-63
Lin, Shih-Chieh (2010) The dynamics of striatum circuitry. Front Integr Neurosci 4:3
Zhang, Hao; Lin, Shih-Chieh; Nicolelis, Miguel A L (2010) Spatiotemporal coupling between hippocampal acetylcholine release and theta oscillations in vivo. J Neurosci 30:13431-40