{"id":27,"date":"2020-09-15T20:58:33","date_gmt":"2020-09-15T20:58:33","guid":{"rendered":"https:\/\/www.renalphysiopathology.com\/?page_id=27"},"modified":"2023-06-05T22:05:22","modified_gmt":"2023-06-05T22:05:22","slug":"original-articles","status":"publish","type":"page","link":"https:\/\/www.renalphysiopathology.com\/publications\/original-articles\/","title":{"rendered":"Original Articles"},"content":{"rendered":"
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Original Articles<\/h1>\t\t\t\t\t
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The Mineralocorticoid Receptor on Smooth Muscle Cells Promotes Tacrolimus-Induced Renal Injury in Mice<\/h3>\n
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The Mineralocorticoid Receptor on Smooth Muscle Cells Promotes Tacrolimus-Induced Renal Injury in Mice<\/h3>\n

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Figueroa S.M., Bertocchio J., Nakamura T., El-Moghrabi S., Jaisser F. and Amador C.A. Pharmaceutics. 2023; 15(5):1373.<\/h4>\n

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Tacrolimus (Tac) is a calcineurin inhibitor commonly used as an immunosuppressor after solid organ transplantation. However, Tac may induce hypertension, nephrotoxicity, and an increase in aldosterone levels. The activation of the mineralocorticoid receptor (MR) is related to the proinflammatory status at the renal level. It modulates the vasoactive response as they are expressed on vascular smooth muscle cells…<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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\u03b1-Ketoglutarate Upregulates Collecting Duct (Pro)renin Receptor Expression, Tubular Angiotensin II Formation, and Na+ Reabsorption During High Glucose Conditions<\/h3>\n
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\u03b1-Ketoglutarate Upregulates Collecting Duct (Pro)renin Receptor Expression, Tubular Angiotensin II Formation, and Na+ Reabsorption During High Glucose Conditions<\/h3>\n

Guerrero A., Visniauskas B., C\u00e1rdenas P., Figueroa S.M., Vivanco J., Salinas-Parra N., Araos P., Nguyen Q.M., Kassan M., Amador C.A., Prieto M.C. and Gonzalez A.A. Frontiers in Cardiovascular Medicine. 2021; 8:644797.<\/h4>\n

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Diabetes mellitus (DM) causes high glucose (HG) levels in the plasma and urine. The (pro)renin receptor (PRR) is a key regulator of renal Na+ handling. PRR is expressed in intercalated (IC) cells of the collecting duct (CD) and binds renin to promote angiotensin (Ang) II formation, thereby contributing to Na+ reabsorption. In DM, the Kreb\u2019s cycle is in a state of suppression in most tissues. However, …<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Upregulation of Cortical Renin and Downregulation of Medullary (Pro) Renin Receptor in Unilateral Ureteral Obstruction<\/h3>\n
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Upregulation of Cortical Renin and Downregulation of Medullary (Pro) Renin Receptor in Unilateral Ureteral Obstruction<\/h3>\n

Figueroa S.M., Lozano M., Lobos C., Hennrikus M.T., Gonzalez A.A., Amador C.A. Frontiers in Pharmacology. 2019; 14(10):1314. PMID: 31803050<\/h4>\n

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Chronic kidney disease (CKD) is characterized by renal dysfunction, which is a common feature of other major diseases, such as hypertension and diabetes. Unilateral ureteral obstruction (UUO) has been used as a model of CKD in experimental animals and consists of total obstruction of one kidney ureter. The UUO decreases renal blood flow, which promotes the synthesis of renin in the juxtaglomerular apparatus…<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Dendritic cells are crucial for cardiovascular remodeling and modulate neutrophil gelatinase- associated lipocalin expression upon mineralocorticoid receptor activation<\/h3>\n
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\nDendritic cells are crucial for cardiovascular remodeling and modulate neutrophil gelatinase- associated lipocalin expression upon mineralocorticoid receptor activation<\/p>\n<\/h3>\n

\nAraos P., Prado C., Lozano M., Figueroa S., Espinoza A., Berger T., Mak T., Jaisser F., Pacheco R., Michea L., Amador C.A. Journal of Hypertension. 2019; 37(7):1482-1492. PMID: 31033725<\/p>\n<\/h4>\n

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\nAdaptive immunity is crucial in cardiovascular and renal inflammation\/fibrosis upon hyperactivation of mineralocorticoid receptor. We have previously demonstrated that dendritic cells can respond to mineralocorticoid receptor activation, and the neutrophil gelatinase-associated lipocalin (NGAL) in dendritic cells is highly increased during aldosterone (Aldo)\/mineralocorticoid receptor-dependent cardiovascular damage…<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Deletion of mineralocorticoid receptors in smooth muscle cells blunts renal vascular resistance following acute cyclosporine administration<\/h3>\n
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\nDeletion of mineralocorticoid receptors in smooth muscle cells blunts renal vascular resistance following acute cyclosporine administration<\/p>\n<\/h3>\n

\nAmador C., Bertocchio J.P., Andr\u00e9-Gr\u00e9goire G., Placier S., Duong Van Huyen J.P., El Moghrabi S., Berger S., Warnock D., Chatziantoniou C., Jaffe I., Rieu P., Jaisser F.. Kidney International. 2016; 89(2): 354-62. PMID: 26422501<\/p>\n<\/h4>\n

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\nCalcineurin inhibitors such as cyclosporine A (CsA) are still commonly used after renal transplantation, despite CsA\u2013induced nephrotoxicity (CIN), which is partly related to vasoactive mechanisms. The mineralocorticoid receptor (MR) is now recognized as a key player in the control of vascular tone, and both endothelial cell- and vascular smooth muscle cell (SMC)-MR modulate the vasoactive responses to vasodilators and …<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Spironolactone decreases DOCA-salt-induced organ damage by blocking the activation of T helper 17 and the downregulation of regulatory T lymphocytes.<\/h3>\n
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\nSpironolactone decreases DOCA-salt-induced organ damage by blocking the activation of T helper 17 and the downregulation of regulatory T lymphocytes.<\/p>\n<\/h3>\n

\nAmador C.A., Barrientos V., Pe\u00f1a J., Herrada A.A., Gonz\u00e1lez M., Vald\u00e9s S., Carrasco L., Alzamora R., Figueroa F., Kalergis A.M., Michea L. Hypertension. 2014; 63(4): 797-803. PMID: 24420551<\/p>\n<\/h4>\n

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\nAdaptive immune response has been implicated in inflammation and fibrosis as a result of exposure to mineralocorticoids and a high-salt diet. We hypothesized that in mineralocorticoid-salt\u2013induced hypertension, activation of the mineralocorticoid receptor alters the T-helper 17 lymphocyte (Th17)\/regulatory T-lymphocyte\/interleukin-17 (IL-17) pathway, contributing to cardiac and renal damage. We studied the …<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Neutrophil Gelatinase\u2013Associated Lipocalin, a Novel Mineralocorticoid Biotarget, Mediates Vascular Profibrotic Effects of Mineralocorticoids<\/h3>\n
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Neutrophil Gelatinase\u2013Associated Lipocalin, a Novel Mineralocorticoid Biotarget, Mediates Vascular Profibrotic Effects of Mineralocorticoids<\/h3>\n

Tarjus A., Mart\u00ednez E., Amador C., Latouche C., El Moghrabi S., Berger T., Wah Mak T., Fay R., Farman N., Rossignol P., Zannad F., L\u00f3pez N., Jaisser F. Hypertension. 2015; 66(1): 158-66. PMID: 25987661<\/h4>\n

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Activation of the mineralocorticoid receptor has been shown to be deleterious in cardiovascular diseases (CVDs). We have recently shown that lipocalin 2 (Lcn2), or neutrophil gelatinase\u2013associated lipocalin (NGAL), is a primary target of aldosterone\/mineralocorticoid receptor in the cardiovascular system. Lcn2 is a circulating protein, which binds matrix metalloproteinase 9 and modulates its stability. We hypothesized that Lcn2 could be a mediator of …<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Neutrophil Gelatinase-Associated Lipocalin from immune cells is mandatory for aldosterone-induced cardiac remodeling and inflammation<\/h3>\n
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Neutrophil Gelatinase-Associated Lipocalin from immune cells is mandatory for aldosterone-induced cardiac remodeling and inflammation<\/h3>\n

Buonafine M., Mart\u00ednez-Mart\u00ednez E., Amador C, Gravez B., Ibarrola J., Fern\u00e1ndez-Celis A., El Moghrabi S., Rossignol P., L\u00f3pez-Andr\u00e9s N., Jaisser F. Journal of Molecular and Cellular Cardiology. 2018; 115:32-38. PMID: 29289651.<\/h4>\n

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Immune system activation is involved in cardiovascular (CV) inflammation and fibrosis, following activation of the mineralocorticoid receptor (MR). We previously showed that Neutrophil Gelatinase-Associated Lipocalin (NGAL) is a novel target of MR signaling in CV tissue and plays a critical role in aldosterone\/MR-dependent hypertension and fibrosis. We hypothesized that the production of NGAL by immune cells may play an important part in the …<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Myeloid CD11c+ Antigen-Presenting Cells Ablation Prevents Hypertension in Response to Angiotensin II Plus High-Salt Diet.<\/h3>\n
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Myeloid CD11c+ Antigen-Presenting Cells Ablation Prevents Hypertension in Response to Angiotensin II Plus High-Salt Diet.<\/h3>\n

Hevia D., Araos P., Prado C., Fuentes Luppichini E., Rojas M., Alzamora R., Cifuentes-Araneda F., Gonz\u00e1lez A., Amador C.A., Pacheco R., Michea L. Hypertension. 2018; 71(4):709-718. PMID: 29378857.<\/h4>\n

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Increasing evidence shows that antigen-presenting cells (APCs) are involved in the development of inflammation associated to hypertension. However, the potential role of APCs in the modulation of renal sodium transport has not been addressed. We hypothesized that APCs participate in renal sodium transport and, thus, development of high blood pressure in response to angiotensin II plus a high-salt diet. Using transgenic mice that allow the …<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>

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Aldosterone Promotes Autoimmune Damage by Enhancing Th17-Mediated Immunity<\/h3>\n
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\nAldosterone Promotes Autoimmune Damage by Enhancing Th17-Mediated Immunity<\/p>\n<\/h3>\n

\nHerrada A.A., Contreras F.J., Marini N.P., Amador C.A., Gonz\u00e1lez P.A., Cort\u00e9s C.M., Riedel C.A., Carvajal C.A., Figueroa F., Michea L.F., Fardella C.E., Kalergis A.M. J Immunol. 2010; 184(1): 191-202. PMID: 19949098<\/p>\n<\/h4>\n

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\nExcessive production of aldosterone leads to the development of hypertension and cardiovascular disease by generating an inflammatory state that can be promoted by T cell immunity. Because nature and intensity of T cell responses is controlled by dendritic cells (DCs), it is important to evaluate whether the function of these cells can be modulated by aldosterone. In this study we show that aldosterone augmented the activation of …<\/p>\n<\/div>\n<\/div><\/div><\/div><\/div>