Radix Paeoniae Rubra Ameliorates Lupus Nephritis in Lupus-Like Symptoms of Mrl Mice by Reducing Intercellular Cell Adhesion Molecule-1, Vascular Cell Adhesion Molecule-1, and Platelet Endothelial Cell Adhesion Molecule-1 Expression

被引:9
|
作者
Wang, Weijie [1 ]
Cao, Lingyong [2 ]
Wang, Xinchang [1 ]
Fan, Yongsheng [1 ,2 ]
机构
[1] Zhejiang Chinese Med Univ, Dept Rheumatol, Affiliated Hosp 2, Hangzhou 310005, Peoples R China
[2] Zhejiang Chinese Med Univ, Coll Bas Med, Hangzhou, Peoples R China
关键词
Radix Paeoniae Rubra (RPR); MRL/lpr mice; ICAM-1; VCAM-1; PECAM-1; prednisone; RHEUMATOID-ARTHRITIS; ERYTHEMATOSUS; APOPTOSIS; DAMAGE; LEVEL;
D O I
10.2174/1386207323666200517114802
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Objective: Vasculitis is the basic pathological change of systemic lupus erythematosus (SLE). Radix Paeoniae Rubra (RPR), a traditional Chinese herb with the function of reducing blood stasis, has anti-inflammatory and immunoregulatory properties. This study explored the effects of RPR on the kidneys of lupus-like symptoms of mr1 (MRL/lpr) mice from the perspective of intercellular cell adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1) and platelet endothelial cell adhesion molecule-1 (PECAM-1). Methods: Eighteen MRL/lpr lupus model mice were randomly divided into three groups, the model control group, prednisone-treated group, and RPR-treated group, and 6 C57BL/ 6 mice were classified as a control group. After the mice had been treated for 12 weeks, the expression of ICAM-1, VCAM-1 and PECAM-1 in the kidney was determined by immunohistochemistry and Reverse Transcription-Polymerase Chain Reaction (RT-PCR). Results: After 12 weeks, there were significant differences in body weight in the model, prednisone and RPR groups compared with the normal group (P <0.05). Pathological observation: Compared with the model group, the proliferation of inflammatory cells infiltrated glomeruli and interstitial cells in prednisone and RPR groups were reduced, and renal pathological damage was reduced. Compared with the model group, urine protein level of prednisone and RPR groups were reduced with no significance (P> 0.05). The mRNA expression levels of ICAM-1 and VCAM-1 were significantly reduced in the prednisone group and RPR group compared with the model group (P <0.05 or P <0.01). Meanwhile, the immunohistochemistry expressions of ICAM-1 and VCAM1 expressed in the kidney were significantly reduced in the prednisone group and RPR group (P <0.01 or P <0.05). However, The mRNA expression level and the immunohistochemistry expressions of PECAM-1 expressed in the kidney were reduced in each treatment group (prednisone group and RPR group), but these differences were not significant (P>0.05). Conclusions: ICAM-1, VCAM-1 and PECAM-1 expression in the model group was found to be significantly increased. In addition, RPR could reduce the expression of ICAM-1, VCAM-1 and PECAM-1 in MRL/lpr lupus mice as effectively as prednisone, which may result in the dosage reduction of prednisone, thus decreasing the toxicity and improving the efficacy of prednisone based treatment of SLE.
引用
收藏
页码:675 / 683
页数:9
相关论文
共 50 条
  • [31] Inhibitors of vascular cell adhesion molecule-1 expression
    Schreiner, EP
    Oberhauser, B
    Foster, CA
    EXPERT OPINION ON THERAPEUTIC PATENTS, 2003, 13 (02) : 149 - 166
  • [32] Vascular cell adhesion molecule-1 and intracellular adhesion molecule-1 levels in carotid endarerectomy patients
    Lee, JA
    Choudhri, TF
    Connolly, ES
    Hoh, BL
    Quest, DO
    Solomon, RA
    Prestigiacomo, CJ
    Schmidt, AM
    STROKE, 1997, 28 (01) : 158 - 158
  • [33] Vascular cell adhesion molecule-1 is a key adhesion molecule in melanoma cell adhesion to the leptomeninges
    Brandsma, D
    Reijneveld, JC
    Taphoorn, MJB
    de Boer, HC
    Gebbink, MFBG
    Ulfman, LH
    Zwaginga, JJ
    Voest, EE
    LABORATORY INVESTIGATION, 2002, 82 (11) : 1493 - 1502
  • [34] Serum levels of soluble platelet endothelial cell adhesion molecule-1 and vascular cell adhesion molecule-1 are decreased in subjects with autism spectrum disorder
    Kameno, Yosuke
    Iwata, Keiko
    Matsuzaki, Hideo
    Miyachi, Taishi
    Tsuchiya, Kenji J.
    Matsumoto, Kaori
    Iwata, Yasuhide
    Suzuki, Katsuaki
    Nakamura, Kazuhiko
    Maekawa, Masato
    Tsujii, Masatsugu
    Sugiyama, Toshirou
    Mori, Norio
    MOLECULAR AUTISM, 2013, 4
  • [35] ELEVATED CYCLIC-AMP INHIBITS ENDOTHELIAL-CELL SYNTHESIS AND EXPRESSION OF TNF-INDUCED ENDOTHELIAL-LEUKOCYTE ADHESION MOLECULE-1, AND VASCULAR CELL-ADHESION MOLECULE-1, BUT NOT INTERCELLULAR-ADHESION MOLECULE-1
    POBER, JS
    SLOWIK, MR
    DELUCA, LG
    RITCHIE, AJ
    JOURNAL OF IMMUNOLOGY, 1993, 150 (11): : 5114 - 5123
  • [36] Antioxidants inhibit the expression of intercellular cell adhesion molecule-1 and vascular cell adhesion molecule-1 induced by oxidized LDL on human umbilical vein endothelial cells
    Cominacini, L
    Garbin, U
    Fratta Pasini, A
    Davoli, A
    Campagnola, M
    Contessi, GB
    Pastorino, AM
    LoCascio, V
    FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (1-2) : 117 - 127
  • [37] Serum levels of soluble platelet endothelial cell adhesion molecule-1 and vascular cell adhesion molecule-1 are decreased in subjects with autism spectrum disorder
    Yosuke Kameno
    Keiko Iwata
    Hideo Matsuzaki
    Taishi Miyachi
    Kenji J Tsuchiya
    Kaori Matsumoto
    Yasuhide Iwata
    Katsuaki Suzuki
    Kazuhiko Nakamura
    Masato Maekawa
    Masatsugu Tsujii
    Toshirou Sugiyama
    Norio Mori
    Molecular Autism, 4
  • [38] Associations of Circulating Vascular Cell Adhesion Molecule-1 and Intercellular Adhesion Molecule-1 With Long-Term Cardiac Function
    Mathew, Daniel T.
    Peigh, Graham
    Lima, Joao A. C.
    Bielinski, Suzette J.
    Larson, Nicholas B.
    Allison, Matthew A.
    Shah, Sanjiv J.
    Patel, Ravi B.
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2024, 13 (06):
  • [39] Intercellular adhesion molecule-1
    vandeStolpe, A
    vanderSaag, PT
    JOURNAL OF MOLECULAR MEDICINE-JMM, 1996, 74 (01): : 13 - 33
  • [40] CD44, intercellular adhesion molecule-1 and vascular cell adhesion molecule-1: biomarkers in search of validation in lymphomas
    Martin, Peter
    LEUKEMIA & LYMPHOMA, 2012, 53 (01) : 1 - 2