Effect of Goreisan, a Traditional Japanese Medicine, on Rat Hindlimb Lymphedema

被引:0
作者
Kawakami, Zenji [1 ]
Matsubara, Yosuke [1 ]
Ogura, Keisuke [1 ]
Imamura, Sachiko [1 ]
Iizuka, Seiichi [1 ]
Zhang, Nana [1 ]
Matsumoto, Chinami [1 ]
Fujitsuka, Naoki [1 ]
机构
[1] Tsumura & Co, Tsumura Kampo Res Labs, 3586 Yoshiwara,Ami Machi, Inashiki, Ibaraki 3001192, Japan
关键词
goreisan; hindlimb; Kampo; lymphedema; pathophysiology; rat model; FIBROSIS; CANCER; RHIZOMES; BETA;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Secondary lymphedema occurs after cancer surgery involving lymph node dissection owing to the lymphatic system dysfunction. However, the pathophysiology of lymphedema and the molecular pathways involved remain unknown. This study aimed to develop a rat hindlimb lymphedema model and investigate the mechanisms that drive pathophysiology and the effects of the traditional Japanese medicine goreisan on lymphedema. The rat lymphedema model was induced by combination surgeries of popliteal lymph node dissection, skin cautery incision, and fascial ablation coagulation in the right hindlimb using male Wistar rats. The foot volume was significantly increased, and recovery was delayed by combination surgeries. Dermal thickness and dilated lymphatic vessels of the hindlimb were observed on postoperative day 2. The number of infiltrating leukocytes (CD45 (+) cells), including CD4 (+) T-cells, increased in the lymphedema group compared with that in the sham group. The relative mRNA expression and protein levels of interleukin-6 (IL -6), CC chemokine ligand 2 (CCL2), transforming growth factor beta 1 (TGF- beta 1), and Fms-related receptor tyrosine kinase 4 (FLT4) were significantly higher in the lymphedema group than in the sham group. Foot volume was decreased by goreisan, furosemide, and prednisolone treatments. Goreisan diminished the increase in CD4 (+) T-cells, and the same trend was observed for CCL2 and FLT4 expression. In conclusion, the rat hindlimb lymphedema model in this study exhibited increased foot volume, skin-infiltrating cells, and pathological changes accompanied by inflammatory and fibrotic responses, suggesting that the model presented significant clinical features of lymphedema. Goreisan may exert a therapeutic effect on lymphedema by inhibiting CD4(+) T-cell infiltration.
引用
收藏
页码:1179 / 1188
页数:10
相关论文
共 50 条
  • [1] [Anonymous], 2020, LYMPHOLOGY, V53, P3
  • [2] Th2 differentiation is necessary for soft tissue fibrosis and lymphatic dysfunction resulting from lymphedema
    Avraham, Tomer
    Zampell, Jamie C.
    Yan, Alan
    Elhadad, Sonia
    Weitman, Evan S.
    Rockson, Stanley G.
    Bromberg, Jacqueline
    Mehrara, Babak J.
    [J]. FASEB JOURNAL, 2013, 27 (03) : 1114 - 1126
  • [3] A Single 9-Colour Flow Cytometric Method to Characterise Major Leukocyte Populations in the Rat: Validation in a Model of LPS-Induced Pulmonary Inflammation
    Barnett-Vanes, Ashton
    Sharrock, Anna
    Birrell, Mark A.
    Rankin, Sara
    [J]. PLOS ONE, 2016, 11 (01):
  • [4] Preparation of Single-cell Suspensions for Cytofluorimetric Analysis from Different Mouse Skin Regions
    Broggi, Achille
    Cigni, Clara
    Zanoni, Ivan
    Granucci, Francesca
    [J]. JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2016, (110):
  • [5] Pharmacological Treatment of Secondary Lymphedema
    Brown, Stav
    Dayan, Joseph H.
    Coriddi, Michelle
    Campbell, Adana
    Kuonqui, Kevin
    Shin, Jinyeon
    Park, Hyeung Ju
    Mehrara, Babak J.
    Kataru, Raghu P.
    [J]. FRONTIERS IN PHARMACOLOGY, 2022, 13
  • [6] Bruns Frank, 2003, J Support Oncol, V1, P121
  • [7] Atractylodin Suppresses TGF-β-Mediated Epithelial-Mesenchymal Transition in Alveolar Epithelial Cells and Attenuates Bleomycin-Induced Pulmonary Fibrosis in Mice
    Chang, Kai-Wei
    Zhang, Xiang
    Lin, Shih-Chao
    Lin, Yu-Chao
    Li, Chia-Hsiang
    Akhrymuk, Ivan
    Lin, Sheng-Hao
    Lin, Chi-Chien
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (20)
  • [8] Alisol B 23-acetate attenuates CKD progression by regulating the renin-angiotensin system and gut-kidney axis
    Chen, Hua
    Wang, Min-Chang
    Chen, Yuan-Yuan
    Chen, Lin
    Wang, Yan-Ni
    Vaziri, Nosratola D.
    Miao, Hua
    Zhao, Ying-Yong
    [J]. THERAPEUTIC ADVANCES IN CHRONIC DISEASE, 2020, 11
  • [9] IL-6 regulates adipose deposition and homeostasis in lymphedema
    Cuzzone, Daniel A.
    Weitman, Evan S.
    Albano, Nicholas J.
    Ghanta, Swapna
    Savetsky, Ira L.
    Gardenier, Jason C.
    Joseph, Walter J.
    Torrisi, Jeremy S.
    Bromberg, Jacqueline F.
    Olszewski, Waldemar L.
    Rockson, Stanley G.
    Mehrara, Babak J.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2014, 306 (10): : H1426 - H1434
  • [10] Organ fibrosis inhibited by blocking transforming growth factor-β signaling via peroxisome proliferator-activated receptor γ agonists
    Deng, Yi-Lei
    Xiong, Xian-Ze
    Cheng, Nan-Sheng
    [J]. HEPATOBILIARY & PANCREATIC DISEASES INTERNATIONAL, 2012, 11 (05) : 467 - 478