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Updated: Jan 21, 2026

Leprdb Mouse Model of Type 2 Diabetes: Pancreatic Islet Isolation and Live-cell 2-Photon Imaging Of Intact Islets
Published on: May 11, 2015
[Preventive and therapeutic effects of Keluoxin Capsules on early diabetic retinopathy in db/db mice]
Yun Luo1, Shan Lu1, Li-Tao Liu2
1Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences Beijing 100193, China.
Abstract:
The aim of this paper was to investigate the preventive effects of Keluoxin Capsules(KLX) on diabetic retinopathy in db/db mice. One hundred male db/db diabetic mice(45-55 g, 8 weeks) were randomly divided into 5 groups(model, KLX low dose, KLX middle dose, KLX high dose, Dobesilate) and 20 male C57 BL/KsJdb~(+/+) were taken as control group. Body weight and fasting blood-glucose were detected every week. Mice were administrated with saline(control and model group), KLX(780, 1 560, 3 120 mg·kg~(-1)·d~(-1), ig), Dobesilate(195 mg·kg~(-1)·d~(-1), ig) for 20 weeks, respectively. At the end of the administration, optical coherence tomography, fundus fluorescein angiography and electroretinogram of the retina were measured. The eyeball was extirpated and retina was isolated to make paraffin section, followed by HE staining and glial fibrillary acidic protein(GFAP) immunohistochemistry. The results indicated that KLX has no obvious effect on body weight and fasting blood level in db/db mice. However, KLX could significantly regulate the thickness of retinal ganglion layer and inner plexiform layer. KLX was able to remarkably reduce the quantity of diabetic microvessel. Meanwhile, KLX could notably improve retinal function. Moreover, KLX could observably modulate the cell arrangement and edema in each layer. There was no markable difference in retina according to the immunochemistry assay. In the present study, KLX exert marked preventive effects on diabetic retinopathy in db/db mice, which provided an experimental evidence for clinical use.
Insights
Keluoxin Capsules (KLX) show preventive effects against diabetic retinopathy in mice by improving retinal structure and function. KLX did not impact body weight or blood glucose levels but protected against retinal damage.
Area of Science:
- Ophthalmology
- Pharmacology
- Diabetology
Background:
- Diabetic retinopathy is a leading cause of blindness.
- Current treatments have limitations.
- Novel therapeutic strategies are needed.
Purpose of the Study:
- To investigate the preventive effects of Keluoxin Capsules (KLX) on diabetic retinopathy.
- To evaluate KLX's impact on retinal structure, function, and microvasculature in a mouse model.
Main Methods:
- db/db mice were treated with varying doses of KLX or Dobesilate for 20 weeks.
- Retinal structure and function were assessed using optical coherence tomography, fundus fluorescein angiography, and electroretinography.
- Histological analysis included HE staining and GFAP immunohistochemistry.
Main Results:
- KLX did not significantly affect body weight or fasting blood glucose levels.
- KLX treatment significantly improved retinal structure by regulating the thickness of the retinal ganglion and inner plexiform layers.
- KLX reduced microvascular abnormalities and improved retinal function, with no significant changes observed in GFAP immunohistochemistry.
Conclusions:
- Keluoxin Capsules demonstrate marked preventive effects against diabetic retinopathy in db/db mice.
- KLX modulates retinal structure and function, offering a potential therapeutic option.
- Further research is warranted to explore KLX's clinical efficacy.
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