Center for Molecular and Vascular Biology, Katholieke Universiteit Leuven, Leuven, Belgium.
Clin Exp Pharmacol Physiol. 2013 Oct;40(10):689-97. doi: 10.1111/1440-1681.12154.
(1) A potential role for the gelatinases in adipocyte differentiation in vitro and adipose tissue development in vivo was investigated using the gelatinase inhibitor tolylsam ((R)-3-methyl-2-[4-(3-p-tolyl-[1,2,4]oxadiazol-5-yl)-benzenesulphonylamino]-butyric acid). (2) Differentiation of murine 3T3-F442A preadipocytes (12 days after reaching confluence) into mature adipocytes in vitro was promoted in the presence of tolylsam (10-100 μmol/L). (3) De novo development of fat tissue in nude mice injected with preadipocytes and kept on a high-fat diet was significantly impaired following treatment with tolylsam (100 mg/kg per day for 4 weeks). (4) Adipose tissue development in matrix metalloproteinase (MMP)-2 deficient mice, kept on a high-fat diet, was significantly impaired following administration of tolylsam (100 mg/kg per day for 15 weeks). This was associated with markedly enhanced metabolic rate. (5) Treatment of MMP-2-deficient mice with tolylsam (100 mg/kg per day, 15 weeks) was associated with the preservation of collagen and a reduction in blood vessel size in adipose tissues in vivo. (6) Furthermore, plasma levels of triglycerides and free fatty acids were reduced by tolylsam treatment of MMP-2-deficient mice (100 mg/kg per day, 15 weeks), whereas nutrient adsorption in the intestine was not affected. (7) The results of the present study indicate that tolylsam promotes preadipocyte differentiation in vitro, but impairs adipose tissue development in vivo.
(1)本研究利用明胶酶抑制剂托利萨姆((R)-3-甲基-2-[4-(3-对甲苯-[1,2,4]恶二唑-5-基)-苯磺酰氨基]-丁酸),研究其在体外脂肪细胞分化和体内脂肪组织发育中的潜在作用。(2)在存在托利萨姆(10-100 μmol/L)的情况下,促进了体外培养的鼠 3T3-F442A 前脂肪细胞(达到汇合后 12 天)向成熟脂肪细胞的分化。(3)在用高脂肪饮食喂养的裸鼠中,经前脂肪细胞注射后新形成的脂肪组织的发育在托利萨姆(100mg/kg/天,持续 4 周)治疗后明显受损。(4)在用高脂肪饮食喂养的基质金属蛋白酶(MMP)-2 缺陷小鼠中,经托利萨姆(100mg/kg/天,持续 15 周)给药后,脂肪组织的发育明显受损,同时伴随着代谢率的显著提高。(5)用托利萨姆(100mg/kg/天,15 周)治疗 MMP-2 缺陷小鼠与体内脂肪组织中胶原蛋白的保存和血管大小的减少有关。(6)此外,托利萨姆治疗 MMP-2 缺陷小鼠可降低血浆甘油三酯和游离脂肪酸水平(100mg/kg/天,15 周),而肠道的营养吸收不受影响。(7)本研究结果表明,托利萨姆促进了前脂肪细胞的体外分化,但损害了体内脂肪组织的发育。