Kidney Injury from Recurrent Heat Stress and Rhabdomyolysis: Protective Role of Allopurinol and Sodium Bicarbonate
Background: Heat stress and rhabdomyolysis are major risk factors for the occurrence of repeated acute kidney injury in workers exposed to heat and strenuous work. These episodes, in turn, may progress to chronic kidney disease. Objective: The purpose of this study was to test the effect of allopuri...
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Veröffentlicht in: | American journal of nephrology 2018-11, Vol.48 (5), p.339-348 |
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creator | Sánchez-Lozada, Laura-Gabriela García-Arroyo, Fernando E. Gonzaga, Guillermo Silverio, Octaviano Blas-Marron, Mónica G. Muñoz-Jimenez, Itzel Tapia, Edilia Osorio-Alonso, Horacio Madero, Magdalena Roncal-Jiménez, Carlos A. Weiss, Ilana Glaser, Jason Johnson, Richard J. |
description | Background: Heat stress and rhabdomyolysis are major risk factors for the occurrence of repeated acute kidney injury in workers exposed to heat and strenuous work. These episodes, in turn, may progress to chronic kidney disease. Objective: The purpose of this study was to test the effect of allopurinol (AP) and sodium bicarbonate on the kidney injury induced by recurrent heat stress dehydration with concomitant repeated episodes of rhabdomyolysis. Methods: The model consisted of heat stress exposure (1 h, 37°C) plus rhabdomyolysis (R) induced by repetitive IM injections of glycerol (7.5 mL/kg BW days) in the rat. In addition, to replicate the human situation, uricase was inhibited (oxonic acid [OA] 750 mg/K/d) to increase uric acid (UA) levels. Additional groups were treated either with AP 150 mg/L, n = 10, bicarbonate (BC; 160 mM, n = 10), or both (AP + BC, n = 10) in drinking water. We also included 2 control groups consisting of normal controls (N-Ref, n = 5) and uricase-inhibited rats (OA, n = 5) that were not exposed to heat or muscle injury. Groups were studied for 35 days. Results: Uricase-inhibited rats exposed to heat and rhabdomyolysis developed pathway and increased intrarenal oxidative stress and inflammasome activation. Kidney injury could be largely prevented by AP, and also BC, although the treatments were not synergistic. Conclusion: Increased levels of UA may play an important role in the renal alterations induced by heat stress and continuous episodes of rhabdomyolysis. Therefore, treatments aimed to reduce hyperuricemia may help to decrease the renal burden in these conditions. Clinical trials are suggested to test whether this is also true in humans. |
doi_str_mv | 10.1159/000494663 |
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These episodes, in turn, may progress to chronic kidney disease. Objective: The purpose of this study was to test the effect of allopurinol (AP) and sodium bicarbonate on the kidney injury induced by recurrent heat stress dehydration with concomitant repeated episodes of rhabdomyolysis. Methods: The model consisted of heat stress exposure (1 h, 37°C) plus rhabdomyolysis (R) induced by repetitive IM injections of glycerol (7.5 mL/kg BW days) in the rat. In addition, to replicate the human situation, uricase was inhibited (oxonic acid [OA] 750 mg/K/d) to increase uric acid (UA) levels. Additional groups were treated either with AP 150 mg/L, n = 10, bicarbonate (BC; 160 mM, n = 10), or both (AP + BC, n = 10) in drinking water. We also included 2 control groups consisting of normal controls (N-Ref, n = 5) and uricase-inhibited rats (OA, n = 5) that were not exposed to heat or muscle injury. Groups were studied for 35 days. Results: Uricase-inhibited rats exposed to heat and rhabdomyolysis developed pathway and increased intrarenal oxidative stress and inflammasome activation. Kidney injury could be largely prevented by AP, and also BC, although the treatments were not synergistic. Conclusion: Increased levels of UA may play an important role in the renal alterations induced by heat stress and continuous episodes of rhabdomyolysis. Therefore, treatments aimed to reduce hyperuricemia may help to decrease the renal burden in these conditions. Clinical trials are suggested to test whether this is also true in humans.</description><identifier>ISSN: 0250-8095</identifier><identifier>EISSN: 1421-9670</identifier><identifier>DOI: 10.1159/000494663</identifier><identifier>PMID: 30391956</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Acute Kidney Injury - drug therapy ; Acute Kidney Injury - etiology ; Acute Kidney Injury - pathology ; Acute renal failure ; Allopurinol ; Allopurinol - administration & dosage ; Animals ; Complications and side effects ; Disease Models, Animal ; Disease Progression ; Drug therapy ; Glycerol - administration & dosage ; Glycerol - toxicity ; Heat stress disorders ; Heat-Shock Response ; Hot Temperature - adverse effects ; Humans ; Kidney - drug effects ; Kidney - pathology ; Male ; Occupational Exposure - adverse effects ; Original Report: Laboratory Investigation ; Oxidative Stress - drug effects ; Oxonic Acid - administration & dosage ; Rats ; Renal Insufficiency, Chronic - etiology ; Renal Insufficiency, Chronic - pathology ; Renal Insufficiency, Chronic - prevention & control ; Rhabdomyolysis ; Rhabdomyolysis - blood ; Rhabdomyolysis - drug therapy ; Rhabdomyolysis - etiology ; Risk factors ; Sodium Bicarbonate - adverse effects ; Testing ; Treatment Outcome ; Urate Oxidase - antagonists & inhibitors ; Urate Oxidase - metabolism ; Uric Acid - blood ; Uric Acid - metabolism</subject><ispartof>American journal of nephrology, 2018-11, Vol.48 (5), p.339-348</ispartof><rights>2018 S. Karger AG, Basel</rights><rights>2018 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2018 S. Karger AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-35b06433024d0b2fea3f50a1c31438588ad04d977adebbcc7cf4c1a42582ef0f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2423,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30391956$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sánchez-Lozada, Laura-Gabriela</creatorcontrib><creatorcontrib>García-Arroyo, Fernando E.</creatorcontrib><creatorcontrib>Gonzaga, Guillermo</creatorcontrib><creatorcontrib>Silverio, Octaviano</creatorcontrib><creatorcontrib>Blas-Marron, Mónica G.</creatorcontrib><creatorcontrib>Muñoz-Jimenez, Itzel</creatorcontrib><creatorcontrib>Tapia, Edilia</creatorcontrib><creatorcontrib>Osorio-Alonso, Horacio</creatorcontrib><creatorcontrib>Madero, Magdalena</creatorcontrib><creatorcontrib>Roncal-Jiménez, Carlos A.</creatorcontrib><creatorcontrib>Weiss, Ilana</creatorcontrib><creatorcontrib>Glaser, Jason</creatorcontrib><creatorcontrib>Johnson, Richard J.</creatorcontrib><title>Kidney Injury from Recurrent Heat Stress and Rhabdomyolysis: Protective Role of Allopurinol and Sodium Bicarbonate</title><title>American journal of nephrology</title><addtitle>Am J Nephrol</addtitle><description>Background: Heat stress and rhabdomyolysis are major risk factors for the occurrence of repeated acute kidney injury in workers exposed to heat and strenuous work. These episodes, in turn, may progress to chronic kidney disease. Objective: The purpose of this study was to test the effect of allopurinol (AP) and sodium bicarbonate on the kidney injury induced by recurrent heat stress dehydration with concomitant repeated episodes of rhabdomyolysis. Methods: The model consisted of heat stress exposure (1 h, 37°C) plus rhabdomyolysis (R) induced by repetitive IM injections of glycerol (7.5 mL/kg BW days) in the rat. In addition, to replicate the human situation, uricase was inhibited (oxonic acid [OA] 750 mg/K/d) to increase uric acid (UA) levels. Additional groups were treated either with AP 150 mg/L, n = 10, bicarbonate (BC; 160 mM, n = 10), or both (AP + BC, n = 10) in drinking water. We also included 2 control groups consisting of normal controls (N-Ref, n = 5) and uricase-inhibited rats (OA, n = 5) that were not exposed to heat or muscle injury. Groups were studied for 35 days. Results: Uricase-inhibited rats exposed to heat and rhabdomyolysis developed pathway and increased intrarenal oxidative stress and inflammasome activation. Kidney injury could be largely prevented by AP, and also BC, although the treatments were not synergistic. Conclusion: Increased levels of UA may play an important role in the renal alterations induced by heat stress and continuous episodes of rhabdomyolysis. Therefore, treatments aimed to reduce hyperuricemia may help to decrease the renal burden in these conditions. Clinical trials are suggested to test whether this is also true in humans.</description><subject>Acute Kidney Injury - drug therapy</subject><subject>Acute Kidney Injury - etiology</subject><subject>Acute Kidney Injury - pathology</subject><subject>Acute renal failure</subject><subject>Allopurinol</subject><subject>Allopurinol - administration & dosage</subject><subject>Animals</subject><subject>Complications and side effects</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>Drug therapy</subject><subject>Glycerol - administration & dosage</subject><subject>Glycerol - toxicity</subject><subject>Heat stress disorders</subject><subject>Heat-Shock Response</subject><subject>Hot Temperature - adverse effects</subject><subject>Humans</subject><subject>Kidney - drug effects</subject><subject>Kidney - pathology</subject><subject>Male</subject><subject>Occupational Exposure - adverse effects</subject><subject>Original Report: Laboratory Investigation</subject><subject>Oxidative Stress - drug effects</subject><subject>Oxonic Acid - administration & dosage</subject><subject>Rats</subject><subject>Renal Insufficiency, Chronic - etiology</subject><subject>Renal Insufficiency, Chronic - pathology</subject><subject>Renal Insufficiency, Chronic - prevention & control</subject><subject>Rhabdomyolysis</subject><subject>Rhabdomyolysis - blood</subject><subject>Rhabdomyolysis - drug therapy</subject><subject>Rhabdomyolysis - etiology</subject><subject>Risk factors</subject><subject>Sodium Bicarbonate - adverse effects</subject><subject>Testing</subject><subject>Treatment Outcome</subject><subject>Urate Oxidase - antagonists & inhibitors</subject><subject>Urate Oxidase - metabolism</subject><subject>Uric Acid - blood</subject><subject>Uric Acid - metabolism</subject><issn>0250-8095</issn><issn>1421-9670</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0c9rFDEUB_Agil2rB-8iAUH0sPVlkvnlbS1qiwVlq-chk7x0UzPJNskI8987666LBckhED7fBy9fQp4zOGOsbN8BgGhFVfEHZMFEwZZtVcNDsoCihGUDbXlCnqR0C8CKBurH5IQDb1lbVgsSv1jtcaKX_naMEzUxDHSNaowRfaYXKDO9zhFTotJrut7IXodhCm5KNr2n32LIqLL9hXQdHNJg6Mq5sB2j9cH9iVwHbceBfrBKxj54mfEpeWSkS_jscJ-SH58-fj-_WF59_Xx5vrpaKsEhL3nZQyU4h0Jo6AuDkpsSJFOcCd6UTSM1CN3WtdTY90rVygjFpCjKpkADhp-SN_u52xjuRky5G2xS6Jz0GMbUFYwDlHXB-Uxf7emNdNhZb0KOUu14t6r4_IEz3amz_6j5aBysCh6Nnd_vBV7_E9igdHmTghuzDT7dh2_3UMWQUkTTbaMdZJw6Bt2u4u5Y8WxfHtYa-wH1Uf7tdAYv9uCnjDcYj-CQ_w2H3ag7</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Sánchez-Lozada, Laura-Gabriela</creator><creator>García-Arroyo, Fernando E.</creator><creator>Gonzaga, Guillermo</creator><creator>Silverio, Octaviano</creator><creator>Blas-Marron, Mónica G.</creator><creator>Muñoz-Jimenez, Itzel</creator><creator>Tapia, Edilia</creator><creator>Osorio-Alonso, Horacio</creator><creator>Madero, Magdalena</creator><creator>Roncal-Jiménez, Carlos A.</creator><creator>Weiss, Ilana</creator><creator>Glaser, Jason</creator><creator>Johnson, Richard J.</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20181101</creationdate><title>Kidney Injury from Recurrent Heat Stress and Rhabdomyolysis: Protective Role of Allopurinol and Sodium Bicarbonate</title><author>Sánchez-Lozada, Laura-Gabriela ; García-Arroyo, Fernando E. ; Gonzaga, Guillermo ; Silverio, Octaviano ; Blas-Marron, Mónica G. ; Muñoz-Jimenez, Itzel ; Tapia, Edilia ; Osorio-Alonso, Horacio ; Madero, Magdalena ; Roncal-Jiménez, Carlos A. ; Weiss, Ilana ; Glaser, Jason ; Johnson, Richard J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-35b06433024d0b2fea3f50a1c31438588ad04d977adebbcc7cf4c1a42582ef0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acute Kidney Injury - drug therapy</topic><topic>Acute Kidney Injury - etiology</topic><topic>Acute Kidney Injury - pathology</topic><topic>Acute renal failure</topic><topic>Allopurinol</topic><topic>Allopurinol - administration & dosage</topic><topic>Animals</topic><topic>Complications and side effects</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>Drug therapy</topic><topic>Glycerol - administration & dosage</topic><topic>Glycerol - toxicity</topic><topic>Heat stress disorders</topic><topic>Heat-Shock Response</topic><topic>Hot Temperature - adverse effects</topic><topic>Humans</topic><topic>Kidney - drug effects</topic><topic>Kidney - pathology</topic><topic>Male</topic><topic>Occupational Exposure - adverse effects</topic><topic>Original Report: Laboratory Investigation</topic><topic>Oxidative Stress - drug effects</topic><topic>Oxonic Acid - administration & dosage</topic><topic>Rats</topic><topic>Renal Insufficiency, Chronic - etiology</topic><topic>Renal Insufficiency, Chronic - pathology</topic><topic>Renal Insufficiency, Chronic - prevention & control</topic><topic>Rhabdomyolysis</topic><topic>Rhabdomyolysis - blood</topic><topic>Rhabdomyolysis - drug therapy</topic><topic>Rhabdomyolysis - etiology</topic><topic>Risk factors</topic><topic>Sodium Bicarbonate - adverse effects</topic><topic>Testing</topic><topic>Treatment Outcome</topic><topic>Urate Oxidase - antagonists & inhibitors</topic><topic>Urate Oxidase - metabolism</topic><topic>Uric Acid - blood</topic><topic>Uric Acid - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sánchez-Lozada, Laura-Gabriela</creatorcontrib><creatorcontrib>García-Arroyo, Fernando E.</creatorcontrib><creatorcontrib>Gonzaga, Guillermo</creatorcontrib><creatorcontrib>Silverio, Octaviano</creatorcontrib><creatorcontrib>Blas-Marron, Mónica G.</creatorcontrib><creatorcontrib>Muñoz-Jimenez, Itzel</creatorcontrib><creatorcontrib>Tapia, Edilia</creatorcontrib><creatorcontrib>Osorio-Alonso, Horacio</creatorcontrib><creatorcontrib>Madero, Magdalena</creatorcontrib><creatorcontrib>Roncal-Jiménez, Carlos A.</creatorcontrib><creatorcontrib>Weiss, Ilana</creatorcontrib><creatorcontrib>Glaser, Jason</creatorcontrib><creatorcontrib>Johnson, Richard J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sánchez-Lozada, Laura-Gabriela</au><au>García-Arroyo, Fernando E.</au><au>Gonzaga, Guillermo</au><au>Silverio, Octaviano</au><au>Blas-Marron, Mónica G.</au><au>Muñoz-Jimenez, Itzel</au><au>Tapia, Edilia</au><au>Osorio-Alonso, Horacio</au><au>Madero, Magdalena</au><au>Roncal-Jiménez, Carlos A.</au><au>Weiss, Ilana</au><au>Glaser, Jason</au><au>Johnson, Richard J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kidney Injury from Recurrent Heat Stress and Rhabdomyolysis: Protective Role of Allopurinol and Sodium Bicarbonate</atitle><jtitle>American journal of nephrology</jtitle><addtitle>Am J Nephrol</addtitle><date>2018-11-01</date><risdate>2018</risdate><volume>48</volume><issue>5</issue><spage>339</spage><epage>348</epage><pages>339-348</pages><issn>0250-8095</issn><eissn>1421-9670</eissn><abstract>Background: Heat stress and rhabdomyolysis are major risk factors for the occurrence of repeated acute kidney injury in workers exposed to heat and strenuous work. These episodes, in turn, may progress to chronic kidney disease. Objective: The purpose of this study was to test the effect of allopurinol (AP) and sodium bicarbonate on the kidney injury induced by recurrent heat stress dehydration with concomitant repeated episodes of rhabdomyolysis. Methods: The model consisted of heat stress exposure (1 h, 37°C) plus rhabdomyolysis (R) induced by repetitive IM injections of glycerol (7.5 mL/kg BW days) in the rat. In addition, to replicate the human situation, uricase was inhibited (oxonic acid [OA] 750 mg/K/d) to increase uric acid (UA) levels. Additional groups were treated either with AP 150 mg/L, n = 10, bicarbonate (BC; 160 mM, n = 10), or both (AP + BC, n = 10) in drinking water. We also included 2 control groups consisting of normal controls (N-Ref, n = 5) and uricase-inhibited rats (OA, n = 5) that were not exposed to heat or muscle injury. Groups were studied for 35 days. Results: Uricase-inhibited rats exposed to heat and rhabdomyolysis developed pathway and increased intrarenal oxidative stress and inflammasome activation. Kidney injury could be largely prevented by AP, and also BC, although the treatments were not synergistic. Conclusion: Increased levels of UA may play an important role in the renal alterations induced by heat stress and continuous episodes of rhabdomyolysis. Therefore, treatments aimed to reduce hyperuricemia may help to decrease the renal burden in these conditions. Clinical trials are suggested to test whether this is also true in humans.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>30391956</pmid><doi>10.1159/000494663</doi><tpages>10</tpages></addata></record> |
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subjects | Acute Kidney Injury - drug therapy Acute Kidney Injury - etiology Acute Kidney Injury - pathology Acute renal failure Allopurinol Allopurinol - administration & dosage Animals Complications and side effects Disease Models, Animal Disease Progression Drug therapy Glycerol - administration & dosage Glycerol - toxicity Heat stress disorders Heat-Shock Response Hot Temperature - adverse effects Humans Kidney - drug effects Kidney - pathology Male Occupational Exposure - adverse effects Original Report: Laboratory Investigation Oxidative Stress - drug effects Oxonic Acid - administration & dosage Rats Renal Insufficiency, Chronic - etiology Renal Insufficiency, Chronic - pathology Renal Insufficiency, Chronic - prevention & control Rhabdomyolysis Rhabdomyolysis - blood Rhabdomyolysis - drug therapy Rhabdomyolysis - etiology Risk factors Sodium Bicarbonate - adverse effects Testing Treatment Outcome Urate Oxidase - antagonists & inhibitors Urate Oxidase - metabolism Uric Acid - blood Uric Acid - metabolism |
title | Kidney Injury from Recurrent Heat Stress and Rhabdomyolysis: Protective Role of Allopurinol and Sodium Bicarbonate |
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