| First Author | Shinotsuka T | Year | 2023 |
| Journal | Cell Rep Methods | Volume | 3 |
| Issue | 7 | Pages | 100519 |
| PubMed ID | 37533646 | Mgi Jnum | J:347162 |
| Mgi Id | MGI:7616644 | Doi | 10.1016/j.crmeth.2023.100519 |
| Citation | Shinotsuka T, et al. (2023) Stimulated Raman scattering microscopy reveals a unique and steady nature of brain water dynamics. Cell Rep Methods 3(7):100519 |
| abstractText | The biological activities of substances in the brain are shaped by their spatiotemporal dynamics in brain tissues, all of which are regulated by water dynamics. In contrast to solute dynamics, water dynamics have been poorly characterized, owing to the lack of appropriate analytical tools. To overcome this limitation, we apply stimulated Raman scattering multimodal multiphoton microscopy to live brain tissues. The microscopy system allows for the visualization of deuterated water, fluorescence-labeled solutes, and cellular structures at high spatiotemporal resolution, revealing that water moves faster than fluorescent molecules in brain tissues. Detailed analyses demonstrate that water, unlike solutes, diffuses homogeneously in brain tissues without differences between the intra- and the extracellular routes. Furthermore, we find that the water dynamics are steady during development and ischemia, when diffusions of solutes are severely affected. Thus, our approach reveals routes and uniquely robust properties of water diffusion in brain tissues. |
