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
Hauptverfasser: 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.
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container_end_page 348
container_issue 5
container_start_page 339
container_title American journal of nephrology
container_volume 48
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.
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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. 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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. 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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.</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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