Silver jubilee: 25 years of the first demonstration of the direct effect of phosphate on the parathyroid cell.
СтатьяОбзорПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Bover Jordi, Trinidad Pedro, Jara Aquiles, Soler-Majoral Jordi, Martín-Malo Alejandro, Torres Armando, Frazão João, Ureña Pablo, Dusso Adriana, Arana Carolt, Graterol Fredzzia, Romero-González Gregorio, Troya Maribel, Samaniego Diana, D'Marco Luis, Valdivielso José Manuel, Fernández Elvira, Arenas María Dolores, Torregrosa Vicente, Navarro-González Juan F, Lloret María Jesús, Ballarín J A, Bosch Ricardo J, Górriz José L, de Francisco Agl, Gutiérrez Orlando, Ara Jordi, Felsenfeld Arnold, Canalejo Antonio, Almadén Yolanda
Аннотация
Although phosphorus is an essential element for life, it is not found in nature in its native state but rather combined in the form of inorganic phosphates (PO43-), with tightly regulated plasma levels that are associated with deleterious effects and mortality when these are out of bounds. The growing interest in the accumulation of PO43- in human pathophysiology originated in its attributed role in the pathogenesis of secondary hyperparathyroidism (SHPT) in chronic kidney disease. In this article, we review the mechanisms by which this effect was justified and we commemorate the important contribution of a Spanish group led by Dr. M. Rodríguez, just 25 years ago, when they first demonstrated the direct effect of PO43- on the regulation of the synthesis and secretion of parathyroid hormone by maintaining the structural integrity of the parathyroid glands in their original experimental model. In addition to demonstrating the importance of arachidonic acid (AA) and the phospholipase A2-AA pathway as a mediator of parathyroid gland response, these findings were predecessors of the recent description of the important role of PO43- on the activity of the calcium sensor-receptor, and also fueled various lines of research on the importance of PO43- overload not only for the pathophysiology of SHPT but also in its systemic pathogenic role.