Angiogenesis Inhibitor, TNP-470, Prevents Diet-Induced and Genetic Obesity in Mice
Open accessAbstract
Adipose tissue growth has been proposed to involve recruitment of new blood vessels. Here, we test the hypothesis that delivery of an angiogenesis inhibitor in mice may prevent diet-induced obesity, the most common type of obesity in humans. We show that systemic administration of a selective angiogenesis inhibitor, TNP-470 (AGM-1470), prevents obesity in high caloric diet-fed wt mice as well as in genetically leptin-deficient ob/ob mice. Inhibition of obesity in mice by TNP-470 involves a reduction of vascularity in the adipose tissue. This therapeutic strategy appears to selectively affect the growth of adipose tissue as measured by the ratio between total fat and lean body mass. Interestingly, the treatment with TNP-470 results in decreased serum levels of low-density lipoprotein cholesterol. Furthermore, insulin levels are reduced, which indicates increased insulin sensitivity, suggesting that angiogenesis inhibitors may prevent the development of type II diabetes. Our findings suggest that similarly to growth and organogenesis in other tissues, adipose tissue growth is dependent on angiogenesis. Our observations may have conceptual implications for the prevention of obesity and related disorders.
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Chemical angiogenic inhibitors such as angiostatin, endostatin, thalidomide, and VEGFR2-blocking antibody TNP-470 reduce body weight and fat pad mass in diet-induced obese or genetically obese ob/ob mice.
“Chemical angiogenic inhibitors such as angiostatin, endostatin, and thalidomide as well as the VEGFR2-blocking antibody TNP-470, have been tested in diet-induced obese mice or genetically obese ob/ob mice and shown to significantly reduce body weight and fat pad mass (88,89).”
From The ominous triad of adipose tissue dysfunction: inflammation, fibrosis, and impaired angiogenesis. (2017) · cites this paper as [89]
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- Authors
- Bråkenhielm, E., Cao, R., Gao, B., Angelin, B., Cannon, B., Parini, P., & Cao, Y.
- Affiliations
- From the Microbiology and Tumor Biology Center (E.B., R.C., Y.C.), Karolinska Institutet, Stockholm, Sweden; The Wenner-Gren Institute (B.G., B.C.), The Arrhenius Laboratories F3, Stockholm University, Stockholm, Sweden; and Metabolism Unit (B.A., P.P.), Center for Metabolism and Endocrinology, Department of Medicine and Molecular Nutrition, Center for Nutrition and Toxicology, Novum, Karolinska Institutet at Huddinge University Hospital, Stockholm, Sweden.
- Stockholm University (SE)
- Venue
- Circulation Research
- Published
- 2004-06-25
- Volume
- 94
- Issue
- 12
- Pages
- 1579-1588
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- OpenAlex
- W2098387318
- Cited by
- 326
- References
- 38
- Citations by year
- 2026: 5 · 2025: 2 · 2024: 12 · 2023: 13 · 2022: 10 · 2021: 7 · 2020: 10 · 2019: 16 · 2018: 18 · 2017: 22 · 2016: 12 · 2015: 11 · 2014: 22 · 2013: 35 · 2012: 20
- FWCI
- 9.82
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Cancerfonden
- Vetenskapsrådet
- Topics
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Keywords
- TNP-470, angiogenesis inhibitors, diet-induced obesity, genetic obesity, ob/ob mice, leptin deficiency, adipose tissue expansion, LDL cholesterol, insulin sensitivity, type 2 diabetes prevention
- MeSH terms
- O-(Chloroacetylcarbamoyl)fumagillol, Adipose Tissue, Animals, Body Composition, Cattle, Cornea, Cyclohexanes, Dietary Fats, Drug Evaluation, Preclinical, Endothelium, Vascular, Insulin Resistance, Lipids, Male, Mice, Inbred C57BL, Mice, Obese, Obesity, Oxygen Consumption, Sesquiterpenes, Neovascularization, Physiologic, Anti-Obesity Agents, Angiogenesis Inhibitors, 3T3-L1 Cells, Endothelial Cells, Carbohydrate Metabolism, Lipid Metabolism, Mice
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