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Aging Mouse Basic Data Collection Study on Histopathological Evaluation of Liver and Kidney in C57BL/6J and C57BL/6N Mice at 78 Weeks of Age

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Aging Mouse Basic Data Collection Study on Histopathological Evaluation of Liver and Kidney in C57BL/6J and C57BL/6N Mice at 78 Weeks of Age

*C57BL/6J mice cannot be shipped outside of Japan due to licensing agreements. Please consider using our contract research services if you need to use this strain.

Accelerate your understanding of age-related disease with detailed pathological data. This study provides crucial insights into organ-level changes in two key mouse strains, offering a resource for validating hypotheses and advancing your research. Our commitment to open data empowers you to access transparent, peer-reviewed information that can save you valuable time and resources in your experimental design.

Study Overview

This study evaluated histopathological changes in the liver and kidneys of aged C57BL/6J (B6J) and C57BL/6N (B6N) mice provided by CLEA Japan. The objective was to clarify structural changes at the organ level in geriatric mice and provide this information as a fundamental resource for age-related disease research.

With the extension of average lifespans, the need for research on age-related organ disorders, including liver and kidney diseases, is growing. However, there is a lack of fundamental histological information on aged mice. In this study, we selected mice with elevated values in blood biochemistry and urinalysis to conduct a detailed pathological analysis of the liver and kidneys.

Individual Selection - C57BL/6N

Individual Selection C57BL/6N
  • Liver selection: Mouse Nos. 7 and 10, which showed high ALT and AST values.
  • Kidney selection: Mouse Nos. 19 and 24, which showed high urinary protein.
  • Mouse Nos. 1 and 2 were used as controls for both liver and kidney.

Individual Selection - C57BL/6J

Individual Selection C57BL/6J
  • Liver selection: Mouse Nos. 5 and 8, which showed high ALT and AST values.
  • Kidney selection: Mouse Nos. 27 and 28, which showed high urinary protein.
  • Mouse Nos. 1 and 2 were used as controls for both liver and kidney.

Materials and Methods

Animals

  • C57BL/6JJcl (B6J): 30 male mice, started at 62 weeks of age.
  • C57BL/6NJcl (B6N): 30 male mice, started at 64 weeks of age.

Housing Conditions

  • Diet: CE-2 (autoclaved), ad libitum
  • Temperature: 20–26°C, Humidity: 45–70%
  • Lighting: 12-hour light / 12-hour dark cycle
  • Single-caged (M cage)
  • Sterilized water, ad libitum

Study Design

  • Regular body weight measurements: Once every two weeks.
  • Dissection and organ collection/weight measurement at 78 weeks of age.
  • For this study, the liver and kidneys were fixed in formalin for histopathological evaluation.

Individual Selection Criteria

  • Liver evaluation: Two mice with high ALT and AST values, and two control mice.
  • Kidney evaluation: Two mice with high urinary protein, and two control mice.

Evaluation Methods

  • Scoring of pathological changes (+++: severe, ++: moderate, +: mild, ±: very mild, -: normal).
  • Items observed: Liver (vacuolization, hypertrophy, focal necrosis), Kidney (adhesion, enlargement, etc.).

Results

Histopathological Evaluation of Liver and Kidney

Histopathological evaluation overview

Results: Histopathological Evaluation (Liver) C57BL/6N

B6N Liver histopathology

Results: Histopathological Evaluation (Kidney) C57BL/6N

B6N Kidney histopathology
  • Focal necrosis (moderate to severe) was observed in two mice with high ALT/AST values.
  • Findings such as fatty liver and hepatocyte hypertrophy, which may be age-related, were also confirmed.

Results: Histopathological Evaluation (Liver) C57BL/6J

B6J Liver histopathology

Results: Histopathological Evaluation (Kidney) C57BL/6J

B6J Kidney histopathology
  • Focal necrosis was observed in the B6J strain as well, but no clear correlation with blood parameters was found.

Summary

Liver

  • Focal necrosis was observed in two C57BL/6N mice that showed elevated liver function parameters.
  • Focal necrosis was also confirmed in other individuals, including C57BL/6J mice, ranging from moderate to severe, but no correlation with liver function parameters was seen.
  • ⇒ Fatty liver and hepatocyte hypertrophy may be age-related changes.

Kidney

  • Effects on glomeruli were observed, but there was no correlation with urinary protein.
  • (The degree of glomerular injury was more severe in C57BL/6J mice than in C57BL/6N mice.)
  • ⇒ The glomerular findings may also be age-related.
  • No tubular damage was observed in either strain.

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