Evolutionary changes leading to efficient glymphatic circulation in the mammalian brain
Narufumi Kameya,
Itsuki Sakai,
Kengo Saito,
Toshihide Hamabe-Horiike,
Yohei Shinmyo,
Mitsutoshi Nakada,
Satoru Okuda () and
Hiroshi Kawasaki ()
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Narufumi Kameya: Kanazawa University
Itsuki Sakai: Kanazawa University
Kengo Saito: Kanazawa University
Toshihide Hamabe-Horiike: Kanazawa University
Yohei Shinmyo: Kanazawa University
Mitsutoshi Nakada: Kanazawa University
Satoru Okuda: Kanazawa University
Hiroshi Kawasaki: Kanazawa University
Nature Communications, 2024, vol. 15, issue 1, 1-17
Abstract:
Abstract The functional significance of the morphological and genetic changes that occurred in the brain during evolution is not fully understood. Here we show the relationships between evolutionary changes of the brain and glymphatic circulation. We establish a mathematical model to simulate glymphatic circulation in the cerebral hemispheres, and our results show that cortical neurons accumulate in areas of the cerebral hemispheres where glymphatic circulation is highly efficient. We also find that cortical folds markedly enhance the efficiency of glymphatic circulation in the cerebral hemispheres. Furthermore, our in vivo study using ferrets reveals sulcus-dominant cerebrospinal fluid (CSF) influx, which enhances the efficiency of glymphatic circulation in the enlarged cerebral hemispheres of gyrencephalic brains. Sulcus-dominant CSF influx is mediated by preferential expression of aquaporin-4 in sulcal regions, and similar expression patterns of aquaporin-4 are also found in human cerebral hemispheres. These results indicate that evolutionary changes in the cerebral hemispheres are related to improved efficiency of glymphatic circulation. It seems plausible that the efficiency of glymphatic circulation is an important factor determining the evolutionary trajectory of the cerebral hemispheres.
Date: 2024
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-54372-1
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DOI: 10.1038/s41467-024-54372-1
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