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Front Endocrinol (Lausanne) ; 12: 652807, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-33868179

RESUMO

Recurrent spontaneous abortion (RSA) remains a critical and challenging problem in reproduction. To discover novel biomarkers for RSA, ultra performance liquid chromatography/tandem mass spectrometry (UPLC-MS/MS) metabolomics approach was applied to detect RSA serum metabolic profiles and explore its possible pathogenesis and mechanism. The abortion rat model was established, and a metabolomics analysis was performed to evaluate the differentially expressed metabolites between the control and model groups. Immunohistochemistry (IHC), qRT-PCR, and Western blot further examined the expression of Arachidonic acid metabolism-related genes in uterus tissues. To identify arachidonic acid metabolism-related changes in RSA, ELISA's potential mechanisms were further confirmed in serum. Ninety-one metabolites were significantly different between the two groups, as indicated by a VIP ≥1, fold change ≥1. The metabolic pathways involving arachidonic acid metabolism pathway (P = 0.00044) are related to RSA. Verification by experimental showed that compared with the control rats, the expression of the COX-1, COX-2, PTGFR, and TBXA2R genes associated with the arachidonic acid metabolism pathway has significantly increased the uterus and serum of RSA rats (P < 0.05). Regulation of the arachidonic acid metabolism pathway might serve as a promising therapeutic strategy for relieving RSA women's symptoms.


Assuntos
Aborto Habitual/sangue , Ácido Araquidônico/sangue , Cromatografia Líquida de Alta Pressão/métodos , Regulação da Expressão Gênica , Metabolômica/métodos , Prenhez , Espectrometria de Massas em Tandem/métodos , Animais , Ácido Araquidônico/química , Biomarcadores/sangue , Ciclo-Oxigenase 1/sangue , Ciclo-Oxigenase 2/sangue , Feminino , Imuno-Histoquímica , Masculino , Proteínas de Membrana/sangue , Redes e Vias Metabólicas , Metaboloma , Gravidez , Prostaglandinas/sangue , Ratos , Ratos Endogâmicos Lew , Receptores de Prostaglandina/sangue , Receptores de Tromboxano A2 e Prostaglandina H2/sangue
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