Tomographic optical imaging of cortical responses after crossing nerve transfer in mice

• Published in: PloS one Vol. 13; no. 2; p. e0193017
• Main Authors: Maniwa, Keiichi, Yamashita, Haruyoshi, Tsukano, Hiroaki, Hishida, Ryuichi, Endo, Naoto, Shibata, Minoru, Shibuki, Katsuei
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 14-02-2018; Public Library of Science (PLoS)
• Subjects: Biology and Life Sciences; Bone surgery; Brachial plexus; Brain research; Cameras; Cortex (somatosensory); Experiments; Fluorescence; Hemodynamics; Imaging; Injuries; Latency; Medicine; Medicine and Health Sciences; Methods; Mice; Microscopy; Mouse devices; Nerves; Neuroimaging; Neurosurgery; Observations; Optical tomography; Orthopedics; Physical Sciences; Research and Analysis Methods; Sciatic nerve; Somatosensory cortex; Stimulation; Thalamus; Japan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0193017

To understand the neural mechanisms underlying the therapeutic effects of crossing nerve transfer for brachial plexus injuries in human patients, we investigated the cortical responses after crossing nerve transfer in mice using conventional and tomographic optical imaging. The distal cut ends of the left median and ulnar nerves were connected to the central cut ends of the right median and ulnar nerves with a sciatic nerve graft at 8 weeks of age. Eight weeks after the operation, the responses in the primary somatosensory cortex (S1) elicited by vibratory stimulation applied to the left forepaw were visualized based on activity-dependent flavoprotein fluorescence changes. In untreated mice, the cortical responses to left forepaw stimulation were mainly observed in the right S1. In mice with nerve crossing transfer, cortical responses to left forepaw stimulation were observed in the left S1 together with clear cortical responses in the right S1. We expected that the right S1 responses in the untreated mice were produced by thalamic inputs to layer IV, whereas those in the operated mice were mediated by callosal inputs from the left S1 to layer II/III of the right S1. To confirm this hypothesis, we performed tomographic imaging of flavoprotein fluorescence responses by macroconfocal microscopy. Flavoprotein fluorescence responses in layer IV were dominant compared to those in layer II/III in untreated mice. In contrast, responses in layer II/III were dominant compared to those in layer IV in operated mice. The peak latency of the cortical responses in the operated mice was longer than that in the untreated mice. These results confirmed our expectation that drastic reorganization in the cortical circuits was induced after crossing nerve transfer in mice.