Objective:To investigate the influence of diabetes on anterior cruciate ligament(ACL) reconstruction in rabbits and the va-lidity of this animal model. Methods:A total of 36 healthy male New Zealand rabbits were randomly divided into groups A and B. The rabbits in group B were given the injection of alloxan 80 mg/kg via the auricular vein,followed by alloxan 120 mg/kg after 48 hours,and those in group A were given an equal volume of normal saline. After a model of diabetes was established,autologous tendon was used for ACL reconstruction. Gross observation,blood glucose,histology,bone mineral density(BMD),micro-CT,and qRT-PCR were used to observe the influence of diabetes on ACL reconstruction. Results:Gross observation showed that group A had smooth surface and homogeneous texture of the tendon graft in the articular cavity,while group B had rough surface,brittle texture,and yellow color of the tendon graft. From after modeling to 8 weeks after surgery,group B had a significant increase in fasting blood glucose and a significantly higher level of fasting blood glucose than group A(P<0.01). Histological examination showed that at 8 weeks after surgery,group B had significant reductions in the numbers of pancreatic islets and islet cells(P<0.01). At 4 weeks after surgery,group A had significantly higher BMD values of the bone tunnel and the surrounding area than group B(P<0.01);at 8 weeks after surgery,both groups had a significant increase in BMD,and there was a significant difference between the two groups(P<0.01). Micro-CT showed that compared with group B at 4 and 8 weeks after surgery,group A had a significantly smaller cross-sectional area of the bone tunnel than group B(4.544±0.056) mm2,(3.667±0.095) mm2 vs. (4.734±0.044) mm2,(4.247±0.069) mm2,P<0.05. Conclusion:The rabbit model of alloxan-induced diabetes and ACL reconstruction is safe,reliable,economic,and stable. There is a significant reduc-tion in BMD of the bone tunnel and the surrounding area in di-abetic rabbits after ACL reconstruction,which results in de-layed growth of the bone tunnel.