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Vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract (Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain

BACKGROUND: Oxidative stress in atherosclerosis produces H(2)O(2) and triggers the activation of nuclear factor kappa beta (NF-κB) and increase of inducible nitric oxide synthase (iNOS). The formation of vasa vasorum occurs in atherosclerosis. Vasa vasorum angiogenesis is mediated by VEGFR-1 and upr...

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Autores principales: Wihastuti, Titin Andri, Sargowo, Djanggan, Tjokroprawiro, Askandar, Permatasari, Nur, Widodo, Mohammad Aris, Soeharto, Setyowati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149390/
https://www.ncbi.nlm.nih.gov/pubmed/25187725
http://dx.doi.org/10.2147/VHRM.S61736
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author Wihastuti, Titin Andri
Sargowo, Djanggan
Tjokroprawiro, Askandar
Permatasari, Nur
Widodo, Mohammad Aris
Soeharto, Setyowati
author_facet Wihastuti, Titin Andri
Sargowo, Djanggan
Tjokroprawiro, Askandar
Permatasari, Nur
Widodo, Mohammad Aris
Soeharto, Setyowati
author_sort Wihastuti, Titin Andri
collection PubMed
description BACKGROUND: Oxidative stress in atherosclerosis produces H(2)O(2) and triggers the activation of nuclear factor kappa beta (NF-κB) and increase of inducible nitric oxide synthase (iNOS). The formation of vasa vasorum occurs in atherosclerosis. Vasa vasorum angiogenesis is mediated by VEGFR-1 and upregulated by hypoxia-inducible factor-1α (HIF-1α). The newly formed vasa vasorum are fragile and immature and thus increase plaque instability. It is necessary to control vasa vasorum angiogenesis by using mangosteen pericarp antioxidant. This study aims to demonstrate that mangosteen pericarp ethanolic extract can act as vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition in rats given a hypercholesterol diet. METHODS: This was a true experimental laboratory, in vivo posttest with control group design, with 20 Rattus norvegicus Wistar strain rats divided into five groups (normal group, hypercholesterol group, and hypercholesterol groups with certain doses of mangosteen pericarp ethanolic extract: 200, 400, and 800 mg/kg body weight). The parameters of this study were H(2)O(2) measured by using colorimetric analysis, as well as NF-κB, iNOS, and HIF-1α, which were measured by using immunofluorescence double staining and observed with a confocal laser scanning microscope in aortic smooth muscle cell. The angiogenesis of vasa vasorum was quantified from VEGFR-1 level in aortic tissue and confirmed with hematoxylin and eosin staining. RESULTS: Analysis of variance test and Pearson’s correlation coefficient showed mangosteen pericarp ethanolic extract had a significant effect (P<0.05) in decreasing vasa vasorum angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition in hypercholesterol-diet-given R. norvegicus Wistar strain. CONCLUSION: Mangosteen pericarp ethanolic extract 800 mg/kg body weight is proven to decrease vasa vasorum angiogenesis. Similar studies with other inflammatory parameters are encouraged to clarify the mechanism of vasa vasorum angiogenesis inhibition by mangosteen pericarp ethanolic extract.
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spelling pubmed-41493902014-09-03 Vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract (Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain Wihastuti, Titin Andri Sargowo, Djanggan Tjokroprawiro, Askandar Permatasari, Nur Widodo, Mohammad Aris Soeharto, Setyowati Vasc Health Risk Manag Original Research BACKGROUND: Oxidative stress in atherosclerosis produces H(2)O(2) and triggers the activation of nuclear factor kappa beta (NF-κB) and increase of inducible nitric oxide synthase (iNOS). The formation of vasa vasorum occurs in atherosclerosis. Vasa vasorum angiogenesis is mediated by VEGFR-1 and upregulated by hypoxia-inducible factor-1α (HIF-1α). The newly formed vasa vasorum are fragile and immature and thus increase plaque instability. It is necessary to control vasa vasorum angiogenesis by using mangosteen pericarp antioxidant. This study aims to demonstrate that mangosteen pericarp ethanolic extract can act as vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition in rats given a hypercholesterol diet. METHODS: This was a true experimental laboratory, in vivo posttest with control group design, with 20 Rattus norvegicus Wistar strain rats divided into five groups (normal group, hypercholesterol group, and hypercholesterol groups with certain doses of mangosteen pericarp ethanolic extract: 200, 400, and 800 mg/kg body weight). The parameters of this study were H(2)O(2) measured by using colorimetric analysis, as well as NF-κB, iNOS, and HIF-1α, which were measured by using immunofluorescence double staining and observed with a confocal laser scanning microscope in aortic smooth muscle cell. The angiogenesis of vasa vasorum was quantified from VEGFR-1 level in aortic tissue and confirmed with hematoxylin and eosin staining. RESULTS: Analysis of variance test and Pearson’s correlation coefficient showed mangosteen pericarp ethanolic extract had a significant effect (P<0.05) in decreasing vasa vasorum angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition in hypercholesterol-diet-given R. norvegicus Wistar strain. CONCLUSION: Mangosteen pericarp ethanolic extract 800 mg/kg body weight is proven to decrease vasa vasorum angiogenesis. Similar studies with other inflammatory parameters are encouraged to clarify the mechanism of vasa vasorum angiogenesis inhibition by mangosteen pericarp ethanolic extract. Dove Medical Press 2014-08-21 /pmc/articles/PMC4149390/ /pubmed/25187725 http://dx.doi.org/10.2147/VHRM.S61736 Text en © 2014 Wihastuti et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wihastuti, Titin Andri
Sargowo, Djanggan
Tjokroprawiro, Askandar
Permatasari, Nur
Widodo, Mohammad Aris
Soeharto, Setyowati
Vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract (Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain
title Vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract (Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain
title_full Vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract (Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain
title_fullStr Vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract (Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain
title_full_unstemmed Vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract (Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain
title_short Vasa vasorum anti-angiogenesis through H(2)O(2), HIF-1α, NF-κB, and iNOS inhibition by mangosteen pericarp ethanolic extract (Garcinia mangostana Linn) in hypercholesterol-diet-given Rattus norvegicus Wistar strain
title_sort vasa vasorum anti-angiogenesis through h(2)o(2), hif-1α, nf-κb, and inos inhibition by mangosteen pericarp ethanolic extract (garcinia mangostana linn) in hypercholesterol-diet-given rattus norvegicus wistar strain
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4149390/
https://www.ncbi.nlm.nih.gov/pubmed/25187725
http://dx.doi.org/10.2147/VHRM.S61736
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