| Literature DB >> 30513396 |
Kicheon Park1, Wei Chen1, Nora D Volkow2, Craig P Allen1, Yingtian Pan1, Congwu Du3.
Abstract
Cocaine is a highly addictive drug with complex pharmacological effects. Most preclinical imaging studies investigating the effects of cocaine in the brain have been performed under anesthesia, which confounds findings. To tackle this problem, we used optical imaging to compare the effects of cocaine in the awake versus the anesthetized states. For this purpose, we customized an air floating mobile cage to fit the multi-wavelength spectral and laser speckle optical imaging system and implanted a multi-layer cranial window over the mouse somatosensory cortex. Results showed significant differences in neuronal activity and hemodynamics at baseline and in response to cocaine between the awake and the anesthetized states (isoflurane anesthesia). Specifically, 1) at baseline isoflurane dilated cerebral vessels, increased cerebral blood flow and depressed neuronal Ca2+ activity compared to the awake state; 2) acute cocaine (1 mg/kg iv) vasoconstricted blood vessels (arteries and veins) and decreased cerebral blood flow and oxygenated hemoglobin in the anesthetized state but not in the awake condition; 3) cocaine increased the accumulation of mean intracellular Ca2+ in neurons in the anesthetized state but not in the awake condition; and 4) in the awake state acute cocaine increased neuronal activities (increased the frequency of Ca2+ transients) and increased neuronal synchronization. We also corroborated that in the awake state cocaine also disrupted neurovascular coupling. These findings indicate that both vascular and neuronal responses to cocaine are influenced by isoflurane anesthesia, which highlights the importance of imaging awake animals when studying the effects of cocaine or other drugs in the brain.Entities:
Keywords: Addiction; Cerebral blood flow; GCaMP6f; Isoflurane; Neuronal [Ca(2+)](i) activity; Neuronal synchronization; Neurovascular coupling; Oxygenated hemoglobin; Vasoconstriction
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Year: 2018 PMID: 30513396 PMCID: PMC6435283 DOI: 10.1016/j.neuroimage.2018.11.062
Source DB: PubMed Journal: Neuroimage ISSN: 1053-8119 Impact factor: 6.556