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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/11867
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dc.contributor.authorGutan, Oleg-
dc.date.accessioned2020-10-01T16:58:29Z-
dc.date.available2020-10-01T16:58:29Z-
dc.date.issued2016-
dc.identifier.citationGUTAN, Oleg. Angiogenesis of atherosclerotic plaque. In: MedEspera: the 6th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2016, p. 280.en_US
dc.identifier.isbn978-9975-3028-3-8.-
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/11867-
dc.descriptionDepartment of Morphopatology, Nicolae Testemitanu State University of Medicine and Pharmacy, Chisinau, Republic of Moldova, The 6th International Medical Congress for Students and Young Doctorsen_US
dc.description.abstractIntroduction: Atherosclerosis is considered a multifactorial disease with many risk factors: smoking, abuse of alcohol, diabetes, hypertension, dyslipidemia and infection with microorganisms. During angiogenesis in atherosclerotic plaque occurs formation of new vessels to maintain the supply of oxygen and nutrients to the cells of the vascular wall. The growth of new vessel that occurs in the regions of atherosclerotic plaque lesions in course of remodeling is considered predisposal factor to plaque rupture. Materials and Methods: We used morphological analysis and immunohistochemistry to investigate the expression of CD34, SMA (actin smooth muscle cells) and CD105- positive in affected vessels of large caliber (aorta, carotid) and medium (cerebral arteries, coronary) taken during necropsies of deceased patients from atherosclerotic complications and / or metabolic syndrome. In this study we included 17 fragments of human aorta with calcined fibrous plaques, 15carotid artery with less pronounced morphological stenosis, 13 middle cerebral arteries. The morphology of plaques was evaluated on serial sections stained with hematoxylin-eosin and analyzed on optical microscopy. The following antibodies were used for immunohistochemistry: SMA (smooth muscle actin), CD34, CD105. Results: At the intimate, most vessels in the region of atherosclerotic plaque were CD34 positive, at level of fibrous plaque - often, and at adventitia, namely vassa- vasorum were positive for CD34 in small and medium vessels. SMA marker is detected in smooth muscle cells, myofibroblasts, myoepithelial cells and less in pericytes. In the region of plaque and its adjacent areas, adventitia and intimate, CD105 vessel density was higher, and in distant regions of atherosclerotic lesion decreased their density. Conclusions:The role of angiogenesis in atherosclerosis is more complex and depends on the stage of pathological process. Our results show that the method of immunohistochemical with application of specific vascular markers, demonstrates important pathogenetic aspects in atherosclerotic plaque formation. In the development of atherosclerotic plaques and in the process of angiogenesis have an important role mast cells and macrophagestogether with other immunocompetent cells.en_US
dc.language.isoenen_US
dc.publisherMedEsperaen_US
dc.subjectangiogenesisen_US
dc.subjectatherosclerosisen_US
dc.subjectatherosclerotic plaqueen_US
dc.subjectSMAen_US
dc.subjectCD34en_US
dc.subjectCD105en_US
dc.titleAngiogenesis of atherosclerotic plaqueen_US
dc.typeArticleen_US
Appears in Collections:MedEspera 2016

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