» Articles » PMID: 20851520

Assessment of Brain Responses to Innocuous and Noxious Electrical Forepaw Stimulation in Mice Using BOLD FMRI

Overview
Journal Pain
Specialties Neurology
Psychiatry
Date 2010 Sep 21
PMID 20851520
Citations 38
Authors
Affiliations
Soon will be listed here.
Abstract

Functional magnetic resonance imaging (fMRI) using the blood oxygen level-dependent (BOLD) contrast was used to study sensory processing in the brain of isoflurane-anesthetized mice. The use of a cryogenic surface coil in a small animal 9.4T system provided the sensitivity required for detection and quantitative analysis of hemodynamic changes caused by neural activity in the mouse brain in response to electrical forepaw stimulation at different amplitudes. A gradient echo-echo planar imaging (GE-EPI) sequence was used to acquire five coronal brain slices of 0.5mm thickness. BOLD signal changes were observed in primary and secondary somatosensory cortices, the thalamus and the insular cortex, important regions involved in sensory and nociceptive processing. Activation was observed consistently bilateral despite unilateral stimulation of the forepaw. The temporal BOLD profile was segregated into two signal components with different temporal characteristics. The maximum BOLD amplitude of both signal components correlated strongly with the stimulation amplitude. Analysis of the dynamic behavior of the somatosensory 'fast' BOLD component revealed a decreasing signal decay rate constant k(off) with increasing maximum BOLD amplitude (and stimulation amplitude). This study demonstrates the feasibility of a robust BOLD fMRI protocol to study nociceptive processing in isoflurane-anesthetized mice. The reliability of the method allows for detailed analysis of the temporal BOLD profile and for investigation of somatosensory and noxious signal processing in the brain, which is attractive for characterizing genetically engineered mouse models.

Citing Articles

Transcranial Functional Ultrasound Imaging Detects Focused Ultrasound Neuromodulation Induced Hemodynamic Changes in Mouse and Nonhuman Primate Brains .

Aurup C, Bendig J, Blackman S, McCune E, Bae S, Jimenez-Gambin S bioRxiv. 2024; .

PMID: 38559149 PMC: 10979885. DOI: 10.1101/2024.03.08.583971.


Generation of a whole-brain hemodynamic response function and sex-specific differences in cerebral processing of mechano-sensation in mice detected by BOLD fMRI.

Chen H, Lambers H, Nagelmann N, Sandbrink M, Segelcke D, Pogatzki-Zahn E Front Neurosci. 2023; 17:1187328.

PMID: 37700753 PMC: 10493293. DOI: 10.3389/fnins.2023.1187328.


Intrinsic, widefield optical imaging of hemodynamics in rodent models of Alzheimer's disease and neurological injury.

Crouzet C, Phan T, Wilson R, Shin T, Choi B Neurophotonics. 2023; 10(2):020601.

PMID: 37143901 PMC: 10152182. DOI: 10.1117/1.NPh.10.2.020601.


An optimized bioluminescent substrate for non-invasive imaging in the brain.

Su Y, Walker J, Hall M, Klein M, Wu X, Encell L Nat Chem Biol. 2023; 19(6):731-739.

PMID: 36759751 PMC: 10229426. DOI: 10.1038/s41589-023-01265-x.


Wireless charging-mediated angiogenesis and nerve repair by adaptable microporous hydrogels from conductive building blocks.

Hsu R, Li S, Fang J, Lee I, Chu L, Lo Y Nat Commun. 2022; 13(1):5172.

PMID: 36056007 PMC: 9440098. DOI: 10.1038/s41467-022-32912-x.