Cortical O <sub>2</sub> supply and metabolism are suppressed in the aged mice

H Hongyi Kang (Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center) S Sitong Zhou (Department of Chemical Engineering, University of California) M Michael Giannetto (Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center) E Evan D. McConnell (Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center) N Ning Kang (Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center) Q Qian Sun H Hetince Zhao (Department of Ophthalmology, Renaissance School of Medicine at Stony Brook University) H Helen S. Wei (Department of Surgery, College of Medicine, University of Kentucky) K Kevin Kramer (Department of Biomedical Engineering, University of California) Y Yaojun Guo (Department of Chemical Engineering, University of California) J Juliana S. Costa (Department of Anatomy and Bakar Aging Research Institute, University of California) S Saul A. Villeda (Department of Anatomy and Bakar Aging Research Institute, University of California) M Maiken Nedergaard J Jiandi Wan (Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center)

Abstract

Current evidence suggests that the rejuvenating effects of parabiosis on brain function arise from the exchange of blood factors that enhance synaptic plasticity, promote neurogenesis, and reduce neuroinflammation in aged animals. However, aging is also associated with diminished tissue oxygenation. Here, we report that erythrocytes (red blood cells, RBCs) from aged mice exhibit reduced responsiveness to low oxygen tension (PO 2 ) and release O 2 slower than those from young mice. In vivo, sensory stimulation evoked a smaller and delayed capillary RBC flow in aged mice. Although activity-evoked PO 2 dips were diminished in aged mice; experimentally reducing PO 2 to comparable levels did not restore capillary flow in aged mice, consistent with diminished RBC O 2 responsiveness observed ex vivo. Notably, RBCs from aged mice in heterochronic parabiosis pairs (young-aged) displayed faster responses to low PO 2 compared to those from aged mice in isochronic pairs (aged-aged). Together, these findings across multiple levels of analysis demonstrate that aging impairs RBC responsiveness to O 2 and suggest that improved RBC-mediated O 2 delivery contributes to the rejuvenating effects of parabiosis.

Article Details

Volume / Issue Vol. 123, Issue 4
Published January 27, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (14)

H

Hongyi Kang

Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center

S

Sitong Zhou

Department of Chemical Engineering, University of California

M

Michael Giannetto

Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center

E

Evan D. McConnell

Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center

N

Ning Kang

Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center

Q

Qian Sun

H

Hetince Zhao

Department of Ophthalmology, Renaissance School of Medicine at Stony Brook University

H

Helen S. Wei

Department of Surgery, College of Medicine, University of Kentucky

K

Kevin Kramer

Department of Biomedical Engineering, University of California

Y

Yaojun Guo

Department of Chemical Engineering, University of California

J

Juliana S. Costa

Department of Anatomy and Bakar Aging Research Institute, University of California

S

Saul A. Villeda

Department of Anatomy and Bakar Aging Research Institute, University of California

M

Maiken Nedergaard

J

Jiandi Wan

Department of Neurosurgery, Center for Translational Neuromedicine, University of Rochester Medical Center