リゾホスファチジン酸(LPA)がSLEモデルマウスの糸球体腎炎を改善させる

Objective: Lupus nephritis is a typical clinical manifestation of SLE. We previously reported that LPA treatment improves depressive-like behavior and microglial activation in MRL/lpr mice (an animal model of SLE). Thus, we examined the effects of LPA on renal function and glomerulonephritis in MRL/...

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Published in日本薬理学会年会要旨集 p. 2-B-SS11-1
Main Authors 永田, 亘, 小泉, 明穂, 中川, 慶一, 髙橋, さやか, 石塚, 俊晶
Format Journal Article
LanguageJapanese
Published 公益社団法人 日本薬理学会 2022
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ISSN2435-4953
DOI10.1254/jpssuppl.96.0_2-B-SS11-1

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Abstract Objective: Lupus nephritis is a typical clinical manifestation of SLE. We previously reported that LPA treatment improves depressive-like behavior and microglial activation in MRL/lpr mice (an animal model of SLE). Thus, we examined the effects of LPA on renal function and glomerulonephritis in MRL/lpr mice. Method:18-week-old MRL+/+ mice (n=12) were treated with vehicle and 18-week-old MRL/lpr mice (n=24) were treated with vehicle or LPA (1 mg/kg) for 2 weeks. After the treatment, urine and blood samples were collected, and histological examinations were performed. Results and Discussion: The significant increases in daily urinary albumin levels in MRL/lpr mice were lost by LPA treatment. Creatinine in plasma was not significantly different between the three groups. The significant increases in plasma dsDNA antibody levels in MRL/lpr mice were lost by LPA treatment. The increases of CD68-positive cells in the glomerulus were found in MRL/lpr mice and the increases were suppressed by LPA treatment. The PAS-positive rates in MRL/lpr mice were significantly increased compared to MRL+/+ mice and the increases were significantly suppressed by LPA treatment. These results suggest that LPA treatment improves glomerulonephritis and proteinuria in MRL/lpr mice.
AbstractList Objective: Lupus nephritis is a typical clinical manifestation of SLE. We previously reported that LPA treatment improves depressive-like behavior and microglial activation in MRL/lpr mice (an animal model of SLE). Thus, we examined the effects of LPA on renal function and glomerulonephritis in MRL/lpr mice. Method:18-week-old MRL+/+ mice (n=12) were treated with vehicle and 18-week-old MRL/lpr mice (n=24) were treated with vehicle or LPA (1 mg/kg) for 2 weeks. After the treatment, urine and blood samples were collected, and histological examinations were performed. Results and Discussion: The significant increases in daily urinary albumin levels in MRL/lpr mice were lost by LPA treatment. Creatinine in plasma was not significantly different between the three groups. The significant increases in plasma dsDNA antibody levels in MRL/lpr mice were lost by LPA treatment. The increases of CD68-positive cells in the glomerulus were found in MRL/lpr mice and the increases were suppressed by LPA treatment. The PAS-positive rates in MRL/lpr mice were significantly increased compared to MRL+/+ mice and the increases were significantly suppressed by LPA treatment. These results suggest that LPA treatment improves glomerulonephritis and proteinuria in MRL/lpr mice.
Author 中川, 慶一
永田, 亘
小泉, 明穂
石塚, 俊晶
髙橋, さやか
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Snippet Objective: Lupus nephritis is a typical clinical manifestation of SLE. We previously reported that LPA treatment improves depressive-like behavior and...
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SubjectTerms autoimmunity
glomerulus
lysophospholipid
Title リゾホスファチジン酸(LPA)がSLEモデルマウスの糸球体腎炎を改善させる
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