Various endurance training intensities improve GFR and Up-regulate AQP2/GSK3β in lithium-induced nephropathic rats

Abstract Background Lithium is extensively used for mood stabilization in bipolar disorder, but its long-term use can lead to nephrotoxicity, characterized by a reduction in glomerular filtration rate (GFR) and potential progression to end-stage renal disease (ESRD). Exercise has been shown to have...

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Main Authors: Shadan Saberi, Mohammad Amin Rajizadeh, Mohammad Khaksari, Azadeh Saber, Mohammad Akhbari, Soheil Aminizadeh, Forouzan Rafie
Format: Article
Language:English
Published: BMC 2025-02-01
Series:BMC Nephrology
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Online Access:https://doi.org/10.1186/s12882-025-03997-5
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author Shadan Saberi
Mohammad Amin Rajizadeh
Mohammad Khaksari
Azadeh Saber
Mohammad Akhbari
Soheil Aminizadeh
Forouzan Rafie
author_facet Shadan Saberi
Mohammad Amin Rajizadeh
Mohammad Khaksari
Azadeh Saber
Mohammad Akhbari
Soheil Aminizadeh
Forouzan Rafie
author_sort Shadan Saberi
collection DOAJ
description Abstract Background Lithium is extensively used for mood stabilization in bipolar disorder, but its long-term use can lead to nephrotoxicity, characterized by a reduction in glomerular filtration rate (GFR) and potential progression to end-stage renal disease (ESRD). Exercise has been shown to have protective effects on renal function, yet the impact of varying exercise intensities on lithium-induced nephropathy is not well understood. Aim This study aimed to investigate the effects of different intensities of endurance training on kidney function and inflammation in a rat model of lithium-induced nephropathy, focusing on the expression of aquaporin 2 (AQP2), glycogen synthase kinase 3-beta (GSK-3β), and SIRT1. Methods Thirty-five male Wistar rats were divided into five groups: control, lithium-only, lithium with low-intensity exercise (LIT), lithium with medium-intensity exercise (MIT), and lithium with high-intensity exercise (HIT). The lithium-induced nephropathy model was established by administering lithium in food. Exercise groups underwent treadmill training at specified intensities for eight weeks. Fractional excretion of sodium (FENa) was measured, and GFR was evaluated by Cr clearance. ELISA and Western blotting assessed inflammatory markers (TNF-α, IL-10), SIRT1, GSK-3β, and AQP2 expressions in kidney tissues. Results Lithium significantly reduced Cr clearance and increased FENa compared to controls. All exercise intensities improved Cr clearance and reduced FENa, with HIT showing the most significant improvement. Exercise at all intensities reduced TNF-α levels and increased IL-10 levels, with MIT and HIT significantly enhancing SIRT1 levels. Lithium reduced the expression of GSK-3β and AQP2, whereas exercise increased their expression across all intensities. Conclusion Endurance training, particularly at high intensity, significantly mitigates lithium-induced renal impairment by improving GFR, reducing inflammation, and enhancing the expression of renal protective proteins. These findings suggest that tailored exercise regimens could be beneficial for patients undergoing long-term lithium therapy to prevent renal damage. Clinical trial number Not applicable. Graphical Abstract
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spelling doaj-art-51cf23516f204ea994aa9a530ecd10de2025-02-09T12:16:49ZengBMCBMC Nephrology1471-23692025-02-0126111110.1186/s12882-025-03997-5Various endurance training intensities improve GFR and Up-regulate AQP2/GSK3β in lithium-induced nephropathic ratsShadan Saberi0Mohammad Amin Rajizadeh1Mohammad Khaksari2Azadeh Saber3Mohammad Akhbari4Soheil Aminizadeh5Forouzan Rafie6Physiology Research Center, Institute of Neuropharmacology, Kerman University of Medical SciencesPhysiology Research Center, Institute of Neuropharmacology, Kerman University of Medical SciencesEndocrinology and Metabolism Research Center, Kerman University of Medical SciencesPhysiology Research Center, Institute of Neuropharmacology, Kerman University of Medical SciencesPhysiology Research Center, Institute of Neuropharmacology, Kerman University of Medical SciencesPhysiology Research Center, Institute of Neuropharmacology, Kerman University of Medical SciencesNeuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical SciencesAbstract Background Lithium is extensively used for mood stabilization in bipolar disorder, but its long-term use can lead to nephrotoxicity, characterized by a reduction in glomerular filtration rate (GFR) and potential progression to end-stage renal disease (ESRD). Exercise has been shown to have protective effects on renal function, yet the impact of varying exercise intensities on lithium-induced nephropathy is not well understood. Aim This study aimed to investigate the effects of different intensities of endurance training on kidney function and inflammation in a rat model of lithium-induced nephropathy, focusing on the expression of aquaporin 2 (AQP2), glycogen synthase kinase 3-beta (GSK-3β), and SIRT1. Methods Thirty-five male Wistar rats were divided into five groups: control, lithium-only, lithium with low-intensity exercise (LIT), lithium with medium-intensity exercise (MIT), and lithium with high-intensity exercise (HIT). The lithium-induced nephropathy model was established by administering lithium in food. Exercise groups underwent treadmill training at specified intensities for eight weeks. Fractional excretion of sodium (FENa) was measured, and GFR was evaluated by Cr clearance. ELISA and Western blotting assessed inflammatory markers (TNF-α, IL-10), SIRT1, GSK-3β, and AQP2 expressions in kidney tissues. Results Lithium significantly reduced Cr clearance and increased FENa compared to controls. All exercise intensities improved Cr clearance and reduced FENa, with HIT showing the most significant improvement. Exercise at all intensities reduced TNF-α levels and increased IL-10 levels, with MIT and HIT significantly enhancing SIRT1 levels. Lithium reduced the expression of GSK-3β and AQP2, whereas exercise increased their expression across all intensities. Conclusion Endurance training, particularly at high intensity, significantly mitigates lithium-induced renal impairment by improving GFR, reducing inflammation, and enhancing the expression of renal protective proteins. These findings suggest that tailored exercise regimens could be beneficial for patients undergoing long-term lithium therapy to prevent renal damage. Clinical trial number Not applicable. Graphical Abstracthttps://doi.org/10.1186/s12882-025-03997-5Lithium-induced nephropathyEndurance trainingExercise intensityGlomerular filtration rateInflammationAquaporin 2
spellingShingle Shadan Saberi
Mohammad Amin Rajizadeh
Mohammad Khaksari
Azadeh Saber
Mohammad Akhbari
Soheil Aminizadeh
Forouzan Rafie
Various endurance training intensities improve GFR and Up-regulate AQP2/GSK3β in lithium-induced nephropathic rats
BMC Nephrology
Lithium-induced nephropathy
Endurance training
Exercise intensity
Glomerular filtration rate
Inflammation
Aquaporin 2
title Various endurance training intensities improve GFR and Up-regulate AQP2/GSK3β in lithium-induced nephropathic rats
title_full Various endurance training intensities improve GFR and Up-regulate AQP2/GSK3β in lithium-induced nephropathic rats
title_fullStr Various endurance training intensities improve GFR and Up-regulate AQP2/GSK3β in lithium-induced nephropathic rats
title_full_unstemmed Various endurance training intensities improve GFR and Up-regulate AQP2/GSK3β in lithium-induced nephropathic rats
title_short Various endurance training intensities improve GFR and Up-regulate AQP2/GSK3β in lithium-induced nephropathic rats
title_sort various endurance training intensities improve gfr and up regulate aqp2 gsk3β in lithium induced nephropathic rats
topic Lithium-induced nephropathy
Endurance training
Exercise intensity
Glomerular filtration rate
Inflammation
Aquaporin 2
url https://doi.org/10.1186/s12882-025-03997-5
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