Kang Jae-Heon, Jeong In Sun, Kim Min-Young
Inje University Seoul Paik hospital, Seoul 04551, Republic of Korea.
AngioLab, Inc., Daejeon 34016, Republic of Korea.
Evid Based Complement Alternat Med. 2018 May 28;2018:4381205. doi: 10.1155/2018/4381205. eCollection 2018.
Adipose tissue growth is angiogenesis-dependent, and angiogenesis inhibitors can regulate adipose tissue mass by cutting off the blood supply. We examined whether antiangiogenic herbal composition Ob-X can reduce fast-growing abdominal fat, especially visceral fat in humans by inhibiting angiogenesis. Eighty abdominally obese subjects (body mass index: 25-29.9 kg/m, waist circumference: exceeding 90 cm for males and 85 cm for females) participated in a 12-week randomized, double-blind, placebo-controlled human study to evaluate the efficacy and safety of Ob-X. 690 mg of Ob-X was administered orally twice a day. The Ob-X group showed a noticeable reduction in visceral fat of 20.5% after the 12-week treatment as compared to baseline measured by computed tomography. The change in visceral fat in the Ob-X group was statistically significant as compared to the placebo group (p = 0.0495) and 1.9 times higher than in the placebo group. Therefore, angiogenesis inhibitor Ob-X has the potential to improve obesity-related metabolic syndrome by reducing dangerous visceral fat.
脂肪组织的生长依赖于血管生成,血管生成抑制剂可通过切断血液供应来调节脂肪组织的质量。我们研究了抗血管生成草药组合物Ob-X是否能通过抑制血管生成来减少人类快速增长的腹部脂肪,尤其是内脏脂肪。80名腹部肥胖受试者(体重指数:25-29.9kg/m,腰围:男性超过90cm,女性超过85cm)参与了一项为期12周的随机、双盲、安慰剂对照人体研究,以评估Ob-X的疗效和安全性。每天口服两次690mg的Ob-X。与通过计算机断层扫描测量的基线相比,Ob-X组在12周治疗后内脏脂肪明显减少了20.5%。与安慰剂组相比,Ob-X组内脏脂肪的变化具有统计学意义(p=0.0495),且比安慰剂组高1.9倍。因此,血管生成抑制剂Ob-X有潜力通过减少危险的内脏脂肪来改善肥胖相关的代谢综合征。