SCIENCE@home

Inbred C57BL/6J and C57BL/6N mice exhibit differential vascular dysfunction compared to outbred UM-HET3 mice.

Mostafa Sabouri,Xiangyu Zheng,Bryan J Irwin,Zhuoxin Li,Jennifer Berg Sen,Joseph Bernardo,Daniel R Machin

Published 2025 in American Journal of Physiology. Heart and Circulatory Physiology

ABSTRACT

Inbred C57BL/6 mice are the most widely used laboratory mice in biomedical research. There are two C57BL/6 substrains, C57BL/6J and C57BL/6N, that are often used interchangeably incorrectly. We sought to examine vascular function in C57BL/6J and C57BL/6N mice. We observed lower systolic blood pressure and aortic stiffness in C57BL/6N vs. C57BL/6J mice. While acetylcholine-mediated vasodilation was similar between C57BL/6 substrains, flow-mediated vasodilation was greater in C57BL/6N vs. C57BL/6J mice. Aortic structural characteristics were also similar between C57BL/6 substrains. These findings indicate distinct differences in vascular function between C57BL/6 substrains, indicating greater vascular function in C57BL/6N mice. To determine the effect of inbreeding on vascular function in C57BL/6J or C57BL/6N mice, we also measured vascular function in UM-HET3 mice, an outbred genetically diverse strain derived from the C57BL/6 strain. In general, UM-HET3 mice had greater vascular function than either C57BL/6 substrain, demonstrated by lower aortic stiffness, aortic medial cross-sectional area, and aortic collagen content and greater aortic elastin content, acetylcholine-mediated vasodilation, and flow-mediated vasodilation. Notably, systolic blood pressure in C57BL/6N mice was also lower than UM-HET3 mice, while aortic elastin content and flow-mediated vasodilation were similar between C57BL/6N and UM-HET3 mice. Importantly, greater vascular function in UM-HET3 mice was not accompanied by greater measurement variability, as coefficient of variation across all measurements was similar between strains. These findings suggest that the greater vascular function in UM-HET3 mice does not come at the expense of measurement variability, making them a viable alternative to inbred mice in biomedical research.

PUBLICATION RECORD

CITATION MAP

EXTRACTION MAP

CLAIMS

  • No claims are published for this paper.

CONCEPTS

  • No concepts are published for this paper.

REFERENCES

Showing 1-52 of 52 references · Page 1 of 1

CITED BY

  • No citing papers are available for this paper.

Showing 0-0 of 0 citing papers · Page 1 of 1