Resveratrol and quercetin interact to inhibit neointimal hyperplasia in mice with a carotid injury

التفاصيل البيبلوغرافية
العنوان: Resveratrol and quercetin interact to inhibit neointimal hyperplasia in mice with a carotid injury
المؤلفون: Runhua Shi, James J. Kleinedler, Reto Asmis, Alok R. Khandelwal, Tammy R. Dugas, Lynette K. Rogers, Valeria Y. Hebert, Sarah L. Ullevig
المصدر: The Journal of nutrition. 142(8)
سنة النشر: 2012
مصطلحات موضوعية: medicine.medical_specialty, Vascular smooth muscle, Endothelium, Medicine (miscellaneous), Resveratrol, Antioxidants, Monocytes, Macrophage chemotaxis, chemistry.chemical_compound, Mice, Restenosis, Internal medicine, Neointima, Stilbenes, medicine, Animals, Drug Interactions, Platelet activation, Cell Proliferation, Neointimal hyperplasia, Inflammation, Nutrition and Dietetics, Hyperplasia, Chemotaxis, Endothelial Cells, medicine.disease, Tunica intima, Thromboxane B2, medicine.anatomical_structure, Endocrinology, chemistry, Female, Quercetin, Endothelium, Vascular, Carotid Artery Injuries
الوصف: Restenosis is a critical complication of angioplasty and stenting. Restenosis is multifactorial, involving endothelial injury, inflammation, platelet activation, and vascular smooth muscle cell (VSMC) proliferation. Thus, dietary strategies to prevent restenosis likely require the use of more than one agent. Resveratrol (R) and quercetin (Q) are polyphenols that are known to exhibit vascular protective effects. We tested whether R and Q administered in the diet interact to inhibit vessel stenosis in mice with a carotid injury. B6.129 mice were administered a high-fat diet containing 21% fat and 0.2% cholesterol along with R (25 mg/kg), Q (10 mg/kg), or R + Q for 2 wk. A carotid injury was induced and the mice were again administered the enriched diet for 2 wk. Compared with the controls, R significantly decreased stenosis, assessed as an intima:media ratio, by 76%. Although Q treatment alone exhibited no effect, it potentiated the effect of R in that treatment with R + Q significantly decreased the intima:media ratio by 94%. Moreover, this effect was greater than that of R treatment alone (P < 0.05). Although treatments with R, Q, and R + Q significantly affected platelet activation and endothelial function, the responses observed for R + Q were less than additive. Specifically, the effects of R + Q were less than the sum of effects for treatments with R and Q alone. In contrast, treatment with R + Q exhibited more-than-additive effects on inflammatory markers and significant interactions between R and Q were observed. The presence of synergy between R and Q was thus tested in cultures of VSMC and macrophages. Isobolographic analysis revealed that 2:1 molar ratios of R:Q exhibited synergistic inhibition of VSMC proliferation and macrophage chemotaxis. In conclusion, in combination, R and Q can interact to reduce the extent of restenosis, perhaps due to their synergistic inhibition of VSMC proliferation and inflammation.
تدمد: 1541-6100
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20bc9a03594720e73f746b06793de1edTest
https://pubmed.ncbi.nlm.nih.gov/22718033Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....20bc9a03594720e73f746b06793de1ed
قاعدة البيانات: OpenAIRE