Dimethyl Fumarate Reduces Methylglyoxal-derived Carbonyl Stress Through Nrf2/GSH Activation in SH-SY5Y Cells DOI

Shin Koike,

Satori Tsurudome,

Shozo Okano

et al.

Neurochemical Research, Journal Year: 2024, Volume and Issue: 50(1)

Published: Nov. 22, 2024

Language: Английский

NRF2 in kidney physiology and disease DOI Creative Commons

Corry D. Bondi,

Hannah L. Hartman, Roderick J. Tan

et al.

Physiological Reports, Journal Year: 2024, Volume and Issue: 12(5)

Published: Feb. 28, 2024

Abstract The role of NRF2 in kidney biology has received considerable interest over the past decade. transcriptionally controls genes responsible for cellular protection against oxidative and electrophilic stress anti‐inflammatory functions. is expressed throughout plays a salt water handling. In disease, animal studies show that protects tubulointerstitial damage reduces interstitial fibrosis tubular atrophy, may slow progression polycystic disease. However, proteinuric glomerular diseases controversial. Although inducer, bardoxolone methyl (CDDO‐Me), increases filtration rate humans, it not been shown to disease diabetic Alport syndrome. Furthermore, was associated with negative effects on fluid retention, proteinuria, blood pressure. Several replicate findings worsened proteinuria more rapid although controversy exists. It clear further study needed better understand kidney. This review summarizes available data clarify promise risks targeting activity

Language: Английский

Citations

12

Potential role of molecular hydrogen therapy on oxidative stress and redox signaling in chronic kidney disease DOI Open Access
Cai‐Mei Zheng, Yi‐Chou Hou, Min-Tser Liao

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2024, Volume and Issue: 176, P. 116802 - 116802

Published: May 24, 2024

Oxidative stress plays a key role in chronic kidney disease (CKD) development and progression, inducing cell damage, inflammation, fibrosis. However, effective therapeutic interventions to slow down CKD advancement are currently lacking. The multifaceted pharmacological effects of molecular hydrogen (H2) have made it promising avenue. H2 is capable capturing harmful •OH ONOO- while maintaining the crucial reactive oxygen species (ROS) involved cellular signaling. NRF2-KEAP1 system, which manages redox balance, could be used treat CKD. activates this pathway, fortifying antioxidant defenses scavenging ROS counteract oxidative stress. can improve NRF2 signaling by using Wnt/β-catenin pathway indirectly activate mitochondria. Additionally, modulates NF-κB activity regulating status, inhibiting MAPK pathways, Trx levels. Treatment with also attenuates HIF neutralizing bolstering HIF-1α function. Furthermore, affects FOXO factors enhances enzymes. Despite encouraging results bench studies, clinical trials still limited require further investigation. focus review on hydrogen's treating renal diseases, specific regulation, discusses its potential applications.

Language: Английский

Citations

10

Repurposing the familiar: Future treatment options against chronic kidney disease DOI

Rohan Bhadange,

Anil Bhanudas Gaikwad

Journal of Pharmacy and Pharmacology, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 20, 2025

Chronic kidney disease (CKD) is a serious health issue with rising morbidity and mortality rates. Despite advances in understanding its pathophysiology, effective therapeutic options are limited, necessitating innovative treatment approaches. Also, current frontline treatments that available against CKD not uniformly often come significant side effects. Therefore, identifying new targets or improving existing for crucial. Drug repurposing promising strategy the drug discovery process involves screening approved drugs applications. This review discusses pharmacological mechanisms clinical evidence support efficacy of these repurposed drugs. Various classes such as inodilators, endothelin-1 type A (ET-1A) receptor antagonists, bisphosphonates, mineralocorticoid (MR) DNA demethylating agents, nuclear factor erythroid 2-related 2 (NRF2) activators, P2X7 inhibitors, autophagy modulators, hypoxia-inducible factor-prolyl hydroxylase inhibitors (HIF-PHI) discussed could remarkably contribute CKD. The critically examines potential well-established to slow progression enhance patient outcomes. emphasizes importance multidisciplinary approach advancing field repurposing, ultimately paving way therapies patients suffering from

Language: Английский

Citations

1

Vaccarin suppresses diabetic nephropathy through inhibiting the EGFR/ERK1/2 signaling pathway DOI Creative Commons
Xuexue Zhu, Xinyu Meng,

Xinyao Du

et al.

Acta Biochimica et Biophysica Sinica, Journal Year: 2024, Volume and Issue: 56(12), P. 1860 - 1874

Published: Aug. 9, 2024

Diabetic nephropathy (DN) is recognized as one of the primary causes chronic kidney disease and end-stage renal disease. Vaccarin (VAC) confers favorable effects on cardiovascular metabolic diseases, including type 2 diabetes mellitus (T2DM). Nonetheless, potential role mechanism VAC in etiology DN have yet to be completely elucidated. In this study, a classical mouse model T2DM experimentally induced via high-fat diet (HFD)/streptozocin (STZ) regimen. Renal histological changes are assessed H&E staining. Masson staining immunohistochemistry (IHC) employed assess fibrosis. RT-PCR utilized quantify mRNA levels fibrosis, oxidative stress inflammation markers. The malondialdehyde (MDA) reactive oxygen species (ROS), well content glutathione peroxidase (GSH-Px), measured. protein expressions collagen I, TGF-β1, α-SMA, E-cadherin, Nrf2, catalase, SOD3, SOD2, SOD1, p-ERK, p-EGFR (Y845), (Y1173), p-NFκB P65, t-ERK, t-EGFR t-NFκB P65 detected by western blot analysis. Our results reveal that has beneficial effect mice improving function mitigating damage. This achieved through its inhibition inflammatory cytokine overproduction, ROS generation. Moreover, treatment effectively suppresses process epithelial-mesenchymal transition (EMT), crucial characteristic high glucose (HG)-induced HK-2 cells. Network pharmacology analysis molecular docking identify epidermal growth factor receptor (EGFR) target for VAC. Amino acid site mutations Lys-879, Ile-918, Ala-920 EGFR may mediate direct binding EGFR. support these findings, reduces phosphorylation both downstream mediator, extracellular signal-regulated kinase 1/2 (ERK1/2), diabetic kidneys HG-treated Notably, blocking either or ERK1/2 yields benefits similar those observed with treatment. Therefore, study reveals attenuates damage inactivation EGFR/ERK1/2 signaling axis patients.

Language: Английский

Citations

4

Bardoxolone displays potent activity against triple negative breast cancer by inhibiting the TRIP13/STAT3 circuit DOI

Jianhua Deng,

Hongyue Li, Ziyang Liu

et al.

Acta Pharmacologica Sinica, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 12, 2025

Language: Английский

Citations

0

Endothelial NOX5 Obliterates the Reno-Protective Effect of Nox4 Deletion by Promoting Renal Fibrosis via Activation of EMT and ROS-Sensitive Pathways in Diabetes DOI Creative Commons
Karin Jandeleit‐Dahm,

Haritha R. Kankanamalage,

Aozhi Dai

et al.

Antioxidants, Journal Year: 2024, Volume and Issue: 13(4), P. 396 - 396

Published: March 26, 2024

Chronic hyperglycemia induces intrarenal oxidative stress due to the excessive production of reactive oxygen species (ROS), leading a cascade events that contribute development and progression diabetic kidney disease (DKD). NOX5, pro-oxidant NADPH oxidase isoform, has been identified as significant contributor renal ROS in humans. Elevated levels endothelial cell dysfunction associated inflammation, causing increased permeability, which can disrupt ecosystem, progressive albuminuria fibrosis DKD. This study specifically examines contribution cell-specific human NOX5 expression pathology transgenic mouse model additionally compares with previously characterized oxidase, NOX4, terms their relative roles Regardless NOX4 pathway, this found exacerbates injury, fibrosis. is attributed activation mesenchymal transition (EMT) pathway via enhanced formation modulation redox-sensitive factors. These findings underscore potential therapeutic significance inhibition The proposes inhibiting could be promising approach for mitigating DKD strengthens case NOX5-specific inhibitors intervention.

Language: Английский

Citations

2

The Role of Antioxidant Transcription Factor Nrf2 and Its Activating Compounds in Systemic Lupus Erythematosus DOI Creative Commons
Lu Liu, Karina de Leeuw, Harry van Goor

et al.

Antioxidants, Journal Year: 2024, Volume and Issue: 13(10), P. 1224 - 1224

Published: Oct. 11, 2024

Systemic lupus erythematosus (SLE) is a complex autoimmune disease in which kidney involvement, so-called nephritis (LN), common and one of the most severe manifestations. Oxidative stress (OS) may play role pathogenesis LN through exacerbation inflammation immune cell dysfunction/dysregulation. Nuclear factor erythroid 2-related 2 (Nrf2), also known as nuclear erythroid-derived 2-like 2, transcription that humans encoded by NFE2L2 gene regarded central regulator antioxidative response. Nrf2-activating compounds have been shown to alleviate oxidative cells tissues lupus-prone mice. Although precise mechanisms Nrf2 activation on system SLE remain be elucidated, are considered novel therapeutical options suppress OS thereby might activity SLE, especially LN. This review therefore summarizes signaling pathway with describes modulating this potential additional clinical interventions.

Language: Английский

Citations

2

Natural products as Nrf2 modulators for ferroptosis inhibition in renal disease therapy: Recent progress and future prospects DOI
Ruimin Tian, Shan Guo,

Shudong Chen

et al.

Phytomedicine, Journal Year: 2024, Volume and Issue: 136, P. 156342 - 156342

Published: Dec. 24, 2024

Language: Английский

Citations

2

Development of Potential Therapeutic Agents from Black Elderberries (the Fruits of Sambucus nigra L.) DOI Creative Commons
Yulin Ren,

Gunnar Meyer,

Andrew T. Anderson

et al.

Molecules, Journal Year: 2024, Volume and Issue: 29(13), P. 2971 - 2971

Published: June 22, 2024

Elderberry (

Language: Английский

Citations

1

Interplay between the Redox System and Renal Tubular Transport DOI Creative Commons

Xiaolan Wang,

Lianjian Li,

Xianfang Meng

et al.

Antioxidants, Journal Year: 2024, Volume and Issue: 13(10), P. 1156 - 1156

Published: Sept. 24, 2024

The kidney plays a critical role in maintaining the homeostasis of body fluid by filtration metabolic wastes and reabsorption nutrients. Due to overload, vast energy is required through aerobic metabolism, which inevitably leads generation reactive oxygen species (ROS) kidney. Under unstressed conditions, ROS are counteracted antioxidant systems maintained at low levels, involved signal transduction physiological processes. Accumulating evidence indicates that reduction–oxidation (redox) system interacts with renal tubular transport. Redox imbalance or dysfunction transport disease. Here, we discuss outline common feature Importantly, describe key molecules their relationship redox and, finally, summarize impact dysregulation on pathogenesis progression acute chronic

Language: Английский

Citations

1