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In this study, we used a model of induction of polycystic ovaries (<jats:styled-content style=\"fixed-case\">PO<\/jats:styled-content>) in rats by exposure to constant light to study the distribution and variations of glycosylated residues present in the different ovarian structures. Seven biotinylated lectins were used (<jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>on\u2010<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> WGA<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> DBA<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> SBA<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> PNA<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> RCA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">UEA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>) on tissue sections, and detection was performed using the streptavidin\/peroxidase method. In tissue sections was observed an increase in affinity for <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>on\u2010<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content> in the granulosa and theca interna of growing follicles and cysts in animals with <jats:styled-content style=\"fixed-case\">PO<\/jats:styled-content> in relation to the control group. Follicular cysts showed higher affinity for <jats:styled-content style=\"fixed-case\">WGA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">RCA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">I<\/jats:styled-content> which growing follicles in the same group, and there was a decrease in affinity for <jats:styled-content style=\"fixed-case\">PNA<\/jats:styled-content> in the cysts in relation to the growth of follicles in both groups. Atretic follicles in both groups showed greater labelling with lectins <jats:styled-content style=\"fixed-case\">PNA<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> SBA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">RCA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">I<\/jats:styled-content> in relation to healthy follicles. It could also be noted that the zona pellucida of cystic follicles lost the affinity for the lectin <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>on\u2010<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>. There was no staining on follicles in any category with the lectins <jats:styled-content style=\"fixed-case\">DBA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">UEA<\/jats:styled-content>\u2010I, although it was staining in the corpus luteum (control group) and in the mesothelium and interstitial glands of both groups with <jats:styled-content style=\"fixed-case\">DBA<\/jats:styled-content>. These observations probably reflect changes in the glycosaminoglycans present in the different ovarian compartments or in the glycosylation of cellular components essential for proper follicular dynamics.<\/jats:p>","DOI":"10.1111\/rda.12174","type":"journal-article","created":{"date-parts":[[2013,4,18]],"date-time":"2013-04-18T12:09:03Z","timestamp":1366286943000},"page":"850-857","source":"Crossref","is-referenced-by-count":5,"title":["Lectin\u2010Binding Pattern in Ovarian Structures of Rats with Experimental Polycystic Ovaries"],"prefix":"10.1111","volume":"48","author":[{"given":"CG","family":"Barbeito","sequence":"first","affiliation":[{"name":"C\u00e1tedra de Histolog\u00eda y Embriolog\u00eda Facultad de Ciencias Veterinarias Universidad Nacional de La Plata Esperanza Santa Fe Argentina"},{"name":"Concejo Nacional de Investigaciones Cient\u00edficas y T\u00e9cnicas (CONICET) Buenos Aires 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