지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
초록· 키워드
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Objective: The purpose of experimental study was to prove the effects of Boyangmakseong-bang (BYMSB) treatment on cBSA-induced in a MN mouse model.
Methods: We divided mice into 4 groups. The Normal group had no treatment. We used cBSA and induced MN mouse model to the other 3 groups. The Control group was treated with cBSA (9㎎/ ㎏ i.p) only. The second group, named ‘BY-250’, was treated with cBSA (9 ㎎/㎏ i.p) and BYMSB extract (250 ㎎/㎏, p.o). The third group, named ‘BY-500’, was treated with cBSA (9 ㎎/㎏ i.p) and BYMSB extract (500㎎/㎏, p.o). After cBSA and BYMSB extract treatment for 4 weeks, the increase in percentage of body weight, proteinuria, serum albumin, total cholesterol, creatinine and BUN of all groups were measured. The CD3+, CD19+, CD4+, CD8+ cell levels of spleen of all groups were analyzed. IgA, IgG, IgM, IL-1β, TNF-α, IL-6 and IFN-γ levels of all groups were gauged. H&E staining, immunofluorescence staining and electron microscopy of kidney were observed.
Results: BYMSB showed significant decrease in the 24hrs proteinuria, serum total cholesterol, serum IgG levels and BUN levels, and showed significant increase in the serum albumin levels compared with the control group. BYMSB showed increase in the increasing percentage of body weight and IFN-γ levels compared with the control. BYMSB showed decrease in the CD3+ T cells, CD4+ Th cells, IL-1β, TNF-α and IL-6 levels, but did not show significant change compared with the control. BYMSB showed considerable decrease in the thickening of the GBM on H&E staining, deposition of IgG on immunofluorescence staining and deposition of electron-density on electron microscopy of kidney compared with the control.
Conclusions: According to the above results, it is suggested that BYMSB decreases the symptoms of MN induced by cBSA in a mouse model. Therefore BYMSB seems to be applicable to MN in clinical practice.
Methods: We divided mice into 4 groups. The Normal group had no treatment. We used cBSA and induced MN mouse model to the other 3 groups. The Control group was treated with cBSA (9㎎/ ㎏ i.p) only. The second group, named ‘BY-250’, was treated with cBSA (9 ㎎/㎏ i.p) and BYMSB extract (250 ㎎/㎏, p.o). The third group, named ‘BY-500’, was treated with cBSA (9 ㎎/㎏ i.p) and BYMSB extract (500㎎/㎏, p.o). After cBSA and BYMSB extract treatment for 4 weeks, the increase in percentage of body weight, proteinuria, serum albumin, total cholesterol, creatinine and BUN of all groups were measured. The CD3+, CD19+, CD4+, CD8+ cell levels of spleen of all groups were analyzed. IgA, IgG, IgM, IL-1β, TNF-α, IL-6 and IFN-γ levels of all groups were gauged. H&E staining, immunofluorescence staining and electron microscopy of kidney were observed.
Results: BYMSB showed significant decrease in the 24hrs proteinuria, serum total cholesterol, serum IgG levels and BUN levels, and showed significant increase in the serum albumin levels compared with the control group. BYMSB showed increase in the increasing percentage of body weight and IFN-γ levels compared with the control. BYMSB showed decrease in the CD3+ T cells, CD4+ Th cells, IL-1β, TNF-α and IL-6 levels, but did not show significant change compared with the control. BYMSB showed considerable decrease in the thickening of the GBM on H&E staining, deposition of IgG on immunofluorescence staining and deposition of electron-density on electron microscopy of kidney compared with the control.
Conclusions: According to the above results, it is suggested that BYMSB decreases the symptoms of MN induced by cBSA in a mouse model. Therefore BYMSB seems to be applicable to MN in clinical practice.
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UCI(KEPA) : I410-ECN-0101-2014-519-000284443