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Curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus

Systemic lupus erythematosus (SLE) is an autoimmune disorder with prevalent hypertension and renal disease. To avoid side effects of immunosuppressive drugs, alternative therapies are needed. Curcumin has been used in Eastern medicine for its anti‐inflammatory and antioxidant properties. This study...

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Autores principales: Dent, Elena L., Taylor, Erin B., Turbeville, Hannah R., Ryan, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354090/
https://www.ncbi.nlm.nih.gov/pubmed/32652896
http://dx.doi.org/10.14814/phy2.14501
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author Dent, Elena L.
Taylor, Erin B.
Turbeville, Hannah R.
Ryan, Michael J.
author_facet Dent, Elena L.
Taylor, Erin B.
Turbeville, Hannah R.
Ryan, Michael J.
author_sort Dent, Elena L.
collection PubMed
description Systemic lupus erythematosus (SLE) is an autoimmune disorder with prevalent hypertension and renal disease. To avoid side effects of immunosuppressive drugs, alternative therapies are needed. Curcumin has been used in Eastern medicine for its anti‐inflammatory and antioxidant properties. This study tested whether oral curcumin administration attenuates autoimmunity and renal injury during SLE. Female NZBWF1 (model of SLE) and NZW/LacJ (control) mice were administered curcumin (500 mg kg(‐1) day(‐1), oral gavage) for 14 days in two separate groups beginning at either 26 or 32 weeks of age. Body weight and composition were monitored throughout the study. Immune activity was assessed by spleen weight, circulating dsDNA autoantibodies, and B lymphocytes. Renal injury (albumin excretion, glomerulosclerosis, blood urea nitrogen (BUN)) was measured as a hemodynamic function (glomerular filtration rate (GFR), mean arterial pressure (MAP)) in conscious mice. Body weight and composition were maintained in curcumin‐treated SLE mice, but decreased in vehicle‐treated SLE mice. Curcumin‐treated SLE mice had lower spleen weight and renal injury (glomerulosclerosis) compared to vehicle‐treated SLE mice when treatment started at 26 weeks of age. When curcumin treatment started at 32 weeks of age, renal injury (glomerulosclerosis, BUN) was reduced in SLE mice compared to vehicle‐treated SLE mice. GFR was reduced, and MAP was increased in vehicle‐treated SLE mice compared to controls; however, these were not improved with curcumin. No significant changes were observed in curcumin‐treated control mice. These data suggest that curcumin modulates autoimmune activity and may lessen renal injury in female mice with SLE.
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spelling pubmed-73540902020-07-17 Curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus Dent, Elena L. Taylor, Erin B. Turbeville, Hannah R. Ryan, Michael J. Physiol Rep Original Articles Systemic lupus erythematosus (SLE) is an autoimmune disorder with prevalent hypertension and renal disease. To avoid side effects of immunosuppressive drugs, alternative therapies are needed. Curcumin has been used in Eastern medicine for its anti‐inflammatory and antioxidant properties. This study tested whether oral curcumin administration attenuates autoimmunity and renal injury during SLE. Female NZBWF1 (model of SLE) and NZW/LacJ (control) mice were administered curcumin (500 mg kg(‐1) day(‐1), oral gavage) for 14 days in two separate groups beginning at either 26 or 32 weeks of age. Body weight and composition were monitored throughout the study. Immune activity was assessed by spleen weight, circulating dsDNA autoantibodies, and B lymphocytes. Renal injury (albumin excretion, glomerulosclerosis, blood urea nitrogen (BUN)) was measured as a hemodynamic function (glomerular filtration rate (GFR), mean arterial pressure (MAP)) in conscious mice. Body weight and composition were maintained in curcumin‐treated SLE mice, but decreased in vehicle‐treated SLE mice. Curcumin‐treated SLE mice had lower spleen weight and renal injury (glomerulosclerosis) compared to vehicle‐treated SLE mice when treatment started at 26 weeks of age. When curcumin treatment started at 32 weeks of age, renal injury (glomerulosclerosis, BUN) was reduced in SLE mice compared to vehicle‐treated SLE mice. GFR was reduced, and MAP was increased in vehicle‐treated SLE mice compared to controls; however, these were not improved with curcumin. No significant changes were observed in curcumin‐treated control mice. These data suggest that curcumin modulates autoimmune activity and may lessen renal injury in female mice with SLE. John Wiley and Sons Inc. 2020-07-11 /pmc/articles/PMC7354090/ /pubmed/32652896 http://dx.doi.org/10.14814/phy2.14501 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Dent, Elena L.
Taylor, Erin B.
Turbeville, Hannah R.
Ryan, Michael J.
Curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus
title Curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus
title_full Curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus
title_fullStr Curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus
title_full_unstemmed Curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus
title_short Curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus
title_sort curcumin attenuates autoimmunity and renal injury in an experimental model of systemic lupus erythematosus
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7354090/
https://www.ncbi.nlm.nih.gov/pubmed/32652896
http://dx.doi.org/10.14814/phy2.14501
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