Carboxytherapy-Induced Fat loss is Associated with VEGF-Mediated Vascularization

被引:7
|
作者
Park, Jun Ho [1 ]
Wee, Syeo Young [1 ]
Chang, Jiyeon [2 ]
Hong, Sunmin [2 ]
Lee, Ju Hee [3 ]
Cho, Kae Won [2 ]
Choi, Chang Yong [4 ]
机构
[1] Soonchunhyang Univ Hosp, Dept Plast & Reconstruct Surg, Gumi 39371, South Korea
[2] Soonchunhyang Univ, Soonchunhyang Inst Medi Bio Sci SIMS, Cheonan 31151, South Korea
[3] Soonchunhyang Univ, Dept Med Biotechnol, Asan 31583, South Korea
[4] Soonchunhyang Univ Hosp, Dept Plast & Reconstruct Surg, Bucheon 14584, South Korea
基金
新加坡国家研究基金会;
关键词
Carboxytherapy; Adipose tissue; Remodeling; Adipose vasculature; VEGF; CARBON-DIOXIDE THERAPY; PPAR-GAMMA-FGF1; AXIS; ADIPOSE; GROWTH; BEIGE; ADIPOGENESIS; CELLULITE; BROWN; SKIN; CO2;
D O I
10.1007/s00266-018-1222-y
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Carboxytherapy is the transcutaneous administration of CO2 gas for therapeutic purposes. Although this non-surgical procedure has been widely used for reducing localized adiposity, its effectiveness on fat loss in obese patients and its underlying mechanisms remain unclear. Methods C57BL/6 mice were fed with a high-fat diet for 8 weeks to generate obese animal models. Obese mice were randomly assigned to two groups: One group was administered air to both inguinal fat pads (air/air), and the other group was treated with air to the left inguinal fat pad and with CO2 to the right inguinal fat pad (air/CO2). Each group was treated every other day for 2 weeks. Morphological changes and expression levels of genes associated with lipogenesis and vascularization in fat were determined by histological and qRT-PCR analyses. Results Mice treated with air/CO2 showed lower body weights and blood glucose levels compared to air/air-treated mice. Paired comparison analysis revealed that CO2 administration significantly decreased adipose tissue weights and adipocyte sizes compared to air treatment. Additionally, CO2 treatment markedly increased vessel numbers and expressions of Vegfa and Fgf1 genes in adipose tissues. The expressions of Fasn and Fabp4 genes were also modestly reduced in CO2-treated adipose tissue. Moreover, Ucp1 expression, the target gene of VEGF and a key regulator in energy expenditure, was significantly increased in CO2-treated adipose tissue. Conclusions Carboxytherapy is effective in the reduction of localized fat in obese patients which is mechanistically associated with alteration of the vasculature involved in VEGF. No Level Assigned This journal requires that authors assign a level of evidence to each submission to which Evidence-Based Medicine rankings are applicable. This excludes Review Articles, Book Reviews, and manuscripts that concern Basic Science, Animal Studies, Cadaver Studies, and Experimental Studies. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266.
引用
收藏
页码:1681 / 1688
页数:8
相关论文
共 13 条
  • [1] Carboxytherapy-Induced Fat loss is Associated with VEGF-Mediated Vascularization
    Jun Ho Park
    Syeo Young Wee
    Jiyeon Chang
    Sunmin Hong
    Ju Hee Lee
    Kae Won Cho
    Chang Yong Choi
    Aesthetic Plastic Surgery, 2018, 42 : 1681 - 1688
  • [2] VEGF-mediated angiogenesis and vascularization of a fumarate-crosslinked polycaprolactone (PCLF) scaffold
    Wagner, Eric R.
    Parry, Joshua
    Dadsetan, Mahrokh
    Bravo, Dalibel
    Riester, Scott M.
    Van Wijnen, Andre J.
    Yaszemski, Michael J.
    Kakar, Sanjeev
    CONNECTIVE TISSUE RESEARCH, 2018, 59 (06) : 542 - 549
  • [3] The role of tumor-associated macrophages in the radioresistance of esophageal cancer cells via regulation of the VEGF-mediated angiogenic pathway
    Sun, Fei
    Lian, Yingying
    Zhou, Mengyun
    Luo, Judong
    Hu, Lijun
    Wang, Jianlin
    Sun, Zhiqiang
    Yu, Jingping
    IMMUNOLOGIC RESEARCH, 2024, 72 (04) : 727 - 740
  • [4] Salidroside protects cardiomyocyte against hypoxia-induced death: A HIF-1α-activated and VEGF-mediated pathway
    Zhang, Jinping
    Liu, Anheng
    Hou, Rongrong
    Zhang, Juan
    Jia, Xin
    Jiang, Weifeng
    Chen, Jianzong
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2009, 607 (1-3) : 6 - 14
  • [5] Hypoxia-induced and HIF1α-VEGF-mediated tight junction dysfunction in choriocarcinoma cells: Implications for preeclampsia
    Zhang, Yuan
    Zhao, Hai-jun
    Xia, Xin-ru
    Diao, Fei-yang
    Ma, Xiang
    Wang, Jing
    Gao, Li
    Liu, Jie
    Gao, Chao
    Cui, Yu-gui
    Liu, Jia-yin
    CLINICA CHIMICA ACTA, 2019, 489 : 203 - 211
  • [6] VEGF-mediated NF-κB activation protects PC12 cells from damage induced by hypoxia
    Mo, Shi-Jing
    Hong, Jun
    Chen, Xu
    Han, Fang
    Ni, Yin
    Zheng, Yang
    Liu, Jing-Quan
    Xu, Liang
    Li, Qian
    Yang, Xiang-Hong
    Sun, Ren-Hua
    Yin, Xiao-Yu
    NEUROSCIENCE LETTERS, 2016, 610 : 54 - 59
  • [7] 6-sialyllactose ameliorates dihydrotestosterone-induced benign prostatic hyperplasia through suppressing VEGF-mediated angiogenesis
    Kim, Eun-Yeong
    Jin, Bo-Ram
    Chung, Tae-Wook
    Bae, Sung-Jin
    Park, Hyerin
    Ryu, Dongryeol
    Jin, Ling
    An, Hyo-Jin
    Ha, Ki-Tae
    BMB REPORTS, 2019, 52 (09) : 560 - 565
  • [8] BMECs Ameliorate High Glucose-Induced Morphological Aberrations and Synaptic Dysfunction via VEGF-Mediated Modulation of Glucose Uptake in Cortical Neurons
    Yu-Qi Huang
    Xiao Gu
    Xiao Chen
    Yi-Ting Du
    Bin-Chi Chen
    Feng-Yan Sun
    Cellular and Molecular Neurobiology, 2023, 43 : 3575 - 3592
  • [9] BMECs Ameliorate High Glucose-Induced Morphological Aberrations and Synaptic Dysfunction via VEGF-Mediated Modulation of Glucose Uptake in Cortical Neurons
    Huang, Yu-Qi
    Gu, Xiao
    Chen, Xiao
    Du, Yi-Ting
    Chen, Bin-Chi
    Sun, Feng-Yan
    CELLULAR AND MOLECULAR NEUROBIOLOGY, 2023, 43 (07) : 3575 - 3592
  • [10] Loss of APJ mediated β-arrestin signalling improves high-fat diet induced metabolic dysfunction but does not alter cardiac function in mice
    Li, Na
    Ma, Xiaochuan
    Ban, Ting
    Xu, Shaohua
    Ma, Yingli
    Ason, Brandon
    Hu, Liaoyuan A.
    BIOCHEMICAL JOURNAL, 2020, 477 (17) : 3313 - 3327