Title:BHTCM Protects Müller Cells from Diabetic Retinopathy by Reducing
Abnormal Changes of Kir4.1 and AQP4, Suppressing VEGF and IL-1β,
and Enhancing PEDF Production
Volume: 20
Issue: 8
Author(s): Haiyan Wu, Xuejun Xie*, Jie Yang, Xuewei Qin, Ya Mo, Li Wan and Mei Zhang*
Affiliation:
- Department of Ophthalmology, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu,
China
- School of Pharmacy, Chengdu University
of Traditional Chinese Medicine, Chengdu, China
Keywords:
Bushen huoxue traditional Chinese medicine, Müller cells, diabetic retinopathy, advanced glycation end products, dithionite, diabetes.
Abstract:
Background: In the diabetic condition, damage to the Müller cells contributes to the pathogenesis
of diabetic retinopathy.
Aims: This study aimed to investigate the protective effect of Bushen Huoxue, Traditional Chinese Medicine
(BHTCM), on Müller in diabetic retinopathological conditions.
Methods: Primary rat retinal Müller cells (RRMC) were isolated and cultured under high glucose (50
nmol/L). The advanced glycation end products (AGEs) and sodium dithionite were applied to treat highglucose
administrated RRMC to mimic diabetic retinopathological conditions. The effects of BHTCM on
diabetic retinopathological RRMC were evaluated. The expressions of aquaporin-4 (AQP4) and Kir4.1
were determined by double-labeling immunofluorescence and ELISA. Levels of vascular endothelial
growth factor (VEGF), interleukin-1β (IL-1β) and pigment epithelium-derived factor (PEDF) were examined
with ELISA. Lactate dehydrogenase (LDH) activity was also evaluated.
Results: Retinal Müller cells were successfully isolated and identified. RRMC treated with AGEs and
sodium dithionite resulted in the increase of AQP4 and decrease of Kir4.1 in RRMC, increase of VEGF
and IL-1β secretion, increase of LDH activity, decrease of PEDF secretion in culture medium, all of
which, in a dose-dependent or time-dependent manner. Post treating RRMC with AGEs and dithionite,
BHTCM reversed changes in expression of AQP4 and Kir4.1 in RRMC, and reversed VEGF levels,
PEDF and IL-1β secretion in the culture medium. Moreover, BHTCM reversed the decrease of RRMC
cell membrane integrity after AGEs and dithionite treatment.
Conclusion: BHTCM protected Müller cells from diabetic damage by reducing abnormal changes of
Kir4.1 and AQP4, inhibiting VEGF and IL-1β, increasing PEDF production, and maintaining cell membrane
integrity. Therefore, BHTCM is a potential drug for the treatment of diabetic retinopathy, which
can correct the function of Müller cells.