B-ob/ob mice

C57BL/6N-Leptintm1Bcgen/Bcgen • 110172

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B-ob/ob mice

Product nameB-ob/ob mice
Catalog number110172
Strain nameC57BL/6N-Leptintm1Bcgen/Bcgen
Strain backgroundC57BL/6N
AliasesLep (leptin), obese

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  • Targeting strategy
  • Phenotypic analysis
  • Efficacy

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      Targeting strategy
      Model validation and analysis

      The results showed that the body weight of homozygous B-ob/ob mice (-/-) was continuously higher than that of the control group after 4 weeks of age.

      The results showed that the body weight of homozygous B-ob/ob mice (-/-) was continuously higher than that of the control group after 4 weeks of age.

      Efficacy of the anti-human GCGR antibody drug crotedumab in B-ob/ob mice

      Efficacy of the anti-human GCGR antibody drug crotedumab in B-ob/ob mice. (A) Body weight changes in B-ob/ob mice. (B-C) Non-fasting blood glucose and fasting blood glucose measurement. Male B-ob/ob mice, 8-10 weeks old, were randomly assigned to 2 groups of 6-7 animals each. Dosing occurred on Day 0. Non-fasting blood glucose was measured on days 0, 3, and 7, and fasting blood glucose after 6 hours of fasting. (D) Crotedumab improves glucose tolerance. (E) The area under the curve of blood glucose content. Mice were fasted for 6 h under free access to water, fasting blood glucose was measured at the tail tip (0 min), injected intraperitoneally at 2 g/kg, and blood glucose was measured at the indicated times. (Fig. F-G) glucagon and insulin measurements. The results showed that crotedumab had hypoglycemic effects in both fasted and non-fasted states while improving glucose tolerance in B-ob/ob mice. (Fig. Data are mean ± SEM; P ≤ 0.05, P ≤ 0.01, P ≤ 0.001)