Related Experiment Video
Updated: Aug 31, 2026

Preclinical Model of Hind Limb Ischemia in Diabetic Rabbits
Published on: June 2, 2019
The development of the acute inflammatory response to experimental cutaneous mucormycosis in normal and diabetic
Abstract:
The histologic changes associated with the development of the acute inflammatory response to experimental cutaneous mucormycosis were studied at various times from 5 minutes to 24 hours after inoculation into normal rabbits and in rabbits with acute alloxan diabetes and acidosis. In normal animals the response by polymorphonuclear leukocytes began within a few minutes after inoculation, increased rapidly in extent and intensity and reached its peak within 6 to 12 hours. By that time there was also early proliferation of fibroblasts and of large mononuclear cells and these cellular reactions, together with the accumulated granulocytes, began to produce a demarcation of the lesions. Beginning 4 to 6 hours after inoculation the fungus showed some growth but this remained confined to the necrotic center of the lesions. In the diabetic rabbits the onset of the response by polymorphonuclear leukocytes was delayed by several hours, reduced in intensity and was apparently less effective. There was no proliferation of fibroblasts and the lesions were spreading rather than circumscribed. Fungus growth in the tissues began shortly after inoculation, was marked, progressed rapidly, and soon extended beyond the site of inoculation. The large mononuclear cells, however, appeared at about the same time and in equal number in the lesions of both diabetic and non-diabetic animals and showed no morphologic changes. It is concluded that a significant delay and impaired effectiveness of the response by polymorphonuclear leukocytes, a lack of fibroblastic proliferation and an enhanced growth of the fungus lower host resistance to infection with it and are directly consequent on severe alterations in host metabolism.
Insights
Diabetic rabbits show delayed and less effective inflammatory responses to mucormycosis, leading to increased fungal growth and spreading lesions. Impaired polymorphonuclear leukocyte function and lack of fibroblast proliferation reduce host resistance.
Area of Science:
- Mycology
- Immunology
- Pathology
Background:
- Cutaneous mucormycosis is a serious fungal infection.
- Host immune responses are critical in controlling fungal infections.
- Diabetes and acidosis can impair immune function.
Purpose of the Study:
- To investigate the histologic changes during experimental cutaneous mucormycosis.
- To compare the inflammatory response in normal versus diabetic rabbits.
- To understand the role of host metabolism in mucormycosis pathogenesis.
Main Methods:
- Histologic examination of lesions in rabbits at various time points post-inoculation.
- Comparison between normal rabbits and rabbits with alloxan-induced diabetes and acidosis.
- Assessment of polymorphonuclear leukocyte, fibroblast, and mononuclear cell responses.
- Evaluation of fungal growth within the lesions.
Main Results:
- Normal rabbits exhibited a robust polymorphonuclear leukocyte response peaking at 6-12 hours, with fibroblast proliferation and lesion demarcation.
- Diabetic rabbits showed delayed, less intense polymorphonuclear leukocyte response, absent fibroblast proliferation, and spreading lesions.
- Fungal growth was confined in normal rabbits but marked and invasive in diabetic rabbits.
- Large mononuclear cells appeared similarly in both groups without morphologic changes.
Conclusions:
- Impaired polymorphonuclear leukocyte response and lack of fibroblast proliferation in diabetic rabbits significantly lower host resistance.
- Enhanced fungal growth in diabetic rabbits is a direct consequence of altered host metabolism.
- These findings highlight the critical role of host immune status in the outcome of mucormycosis.
