{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T17:16:04Z","timestamp":1792516564125,"version":"4.5.0"},"reference-count":71,"publisher":"Oxford University Press (OUP)","issue":"1","license":[{"start":{"date-parts":[[2024,6,13]],"date-time":"2024-06-13T00:00:00Z","timestamp":1718236800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":["rep.bioscientifica.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2024,7,1]]},"abstract":"<jats:title>\u2003<\/jats:title>\n                  <jats:sec>\n                    <jats:title>In brief<\/jats:title>\n                    <jats:p>The endocrine disruptor, nonylphenol (NP) increases 20:4n-6 release in Sertoli cells via PKA\/cPLA2 activation. Our data show that lipid metabolism could be a target of NP-induced abnormal reproductive outcomes.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Abstract<\/jats:title>\n                    <jats:p>Nonylphenol (NP), an endocrine-disrupting chemical, is an environmental contaminant, and many notorious effects on male fertility have been reported in animal models and wild-type species. Here, we evaluated the effects of NP in follicle-stimulating hormone (FSH) signal transduction pathways and lipid metabolism using an in vitro model of rat Sertoli cell (SC) primary culture. Results show that an acute (1 h) SC exposure to NP (10 \u00b5M) increased the intra- and extra-cellular concentrations of free fatty acids (FFAs), mainly arachidonic acid (20:4n-6). Phosphatidylinositol seemed to be the major phospholipid source of this 20:4n-6 release by activation of the protein kinase A (PKA)\/cytoplasmic phospholipase A2 (cPLA2) pathway. NP also increased diacylglycerols (DAG) levels and the expression (mRNA) of cyclooxygenase 2 (Cox2) and prostaglandin E2 (PGE2) levels. It is noteworthy that accumulation of lipid droplets took place after 24 h NP exposition, which was prevented by both a PKA inhibitor and a PLA2 inhibitor. Like FSH, NP triggers the release of 20:4n-6, which is a substrate for PGE2 synthesis via PKA\/PLA2 activation. In addition, NP induces the formation of DAG, which could be required as a cofactor of the PKC-mediated activation of the COX2 inflammatory pathway. Our findings suggest that NP alters lipid homeostasis in SCs by inducing the activation of pro-inflammatory pathways that may trigger adverse effects in testis physiology over time. Concomitantly, the SC enhances the acylation of surplus FFAs (including 20:4n-6) in neutral lipids as a protective mechanism to shield itself from lipotoxicity and pro-inflammatory signals.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1530\/rep-23-0292","type":"journal-article","created":{"date-parts":[[2024,5,17]],"date-time":"2024-05-17T12:52:11Z","timestamp":1715950331000},"update-policy":"https:\/\/doi.org\/10.1530\/crossmarkpolicy-11","source":"Crossref","is-referenced-by-count":4,"title":["Nonylphenol releases arachidonic acid in rat Sertoli cells via activation of PKA and PLA2"],"prefix":"10.1093","volume":"168","author":[{"given":"Florencia X","family":"Santiago Valtierra","sequence":"first","affiliation":[{"name":"Instituto de Investigaciones Bioqu\u00edmicas de Bah\u00eda Blanca (INIBIBB) , Consejo Nacional de Investigaciones Cient\u00edficas y T\u00e9cnicas (CONICET), Bah\u00eda Blanca, Argentina"},{"name":"Departamento de Biolog\u00eda , Bioqu\u00edmica y Farmacia, Universidad Nacional del Sur (UNS), Bah\u00eda Blanca, Argentina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Paulina","family":"Urriola-Mu\u00f1oz","sequence":"additional","affiliation":[{"name":"Departamento de Fisiolog\u00eda , Pontificia Universidad Cat\u00f3lica de Chile, Santiago, Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rodrigo","family":"Godoy-Sep\u00falveda","sequence":"additional","affiliation":[{"name":"Instituto de Qu\u00edmica , Pontificia Universidad Cat\u00f3lica de Valpara\u00edso, Valpara\u00edso, Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ricardo D","family":"Moreno","sequence":"additional","affiliation":[{"name":"Departamento de Fisiolog\u00eda , Pontificia Universidad Cat\u00f3lica de Chile, Santiago, Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Juan G","family":"Reyes","sequence":"additional","affiliation":[{"name":"Instituto de Qu\u00edmica , Pontificia Universidad Cat\u00f3lica de Valpara\u00edso, Valpara\u00edso, Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ana S","family":"Vall\u00e9s","sequence":"additional","affiliation":[{"name":"Instituto de Investigaciones Bioqu\u00edmicas de Bah\u00eda Blanca (INIBIBB) , Consejo Nacional de Investigaciones Cient\u00edficas y T\u00e9cnicas (CONICET), Bah\u00eda Blanca, Argentina"},{"name":"Departamento de Biolog\u00eda , Bioqu\u00edmica y Farmacia, Universidad Nacional del Sur (UNS), Bah\u00eda Blanca, Argentina"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8297-0999","authenticated-orcid":false,"given":"Gerardo M","family":"Oresti","sequence":"additional","affiliation":[{"name":"Instituto de Investigaciones Bioqu\u00edmicas de Bah\u00eda Blanca (INIBIBB) , Consejo Nacional de Investigaciones Cient\u00edficas y T\u00e9cnicas (CONICET), Bah\u00eda Blanca, Argentina"},{"name":"Departamento de Biolog\u00eda , 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