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Novel Approaches in Chronic Renal Failure without Renal Replacement Therapy: A Review
Sandra Luz Martínez-Hernández1, Martín Humberto Muñoz-Ortega2, Manuel Enrique Ávila-Blanco3
1Departamento de Microbiología, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes, Aguascalientes 20100, Ags, Mexico.
Insights
Novel therapies for chronic kidney disease (CKD) focus on reducing inflammation and fibrosis. Future treatments may include regenerative medicine and targeted drug interventions to halt renal damage.
Area of Science:
- Nephrology
- Pharmacology
- Regenerative Medicine
Background:
- Chronic kidney disease (CKD) involves renal parenchymal damage and reduced glomerular filtration rate.
- Inflammation is a key driver of tissue damage and progression to renal failure in CKD.
- Current CKD treatments manage symptoms but do not halt disease progression.
Purpose of the Study:
- To review novel therapeutic strategies for CKD targeting inflammation, fibrosis, and regeneration.
- To explore mechanisms underlying the proinflammatory and profibrotic state in CKD.
- To identify potential pharmacological interventions for reversing renal damage.
Main Methods:
- Critical review of existing literature on CKD therapeutics.
- Examination of molecular signaling pathways (e.g., TGF-β, Smad, Nrf2) involved in renal inflammation and fibrosis.
- Analysis of emerging treatment modalities including vaptans, antifibrotics, antioxidants, stem cell therapy, and probiotics.
Main Results:
- Novel approaches aim to ameliorate inflammation and extracellular matrix accumulation.
- Understanding disease mechanisms may lead to targeted pharmacological interventions.
- Combination therapies show potential for reversing renal damage in CKD.
Conclusions:
- The non-replacement phase of CKD lacks effective treatments.
- Future research directions include vaptans, antifibrotic agents, antioxidants, stem cells, and probiotics.
- Targeting specific molecular pathways offers promise for mitigating renal damage in CKD.
Abstract:
Chronic kidney disease (CKD) is characterized by renal parenchymal damage leading to a reduction in the glomerular filtration rate. The inflammatory response plays a pivotal role in the tissue damage contributing to renal failure. Current therapeutic options encompass dietary control, mineral salt regulation, and management of blood pressure, blood glucose, and fatty acid levels. However, they do not effectively halt the progression of renal damage. This review critically examines novel therapeutic avenues aimed at ameliorating inflammation, mitigating extracellular matrix accumulation, and fostering renal tissue regeneration in the context of CKD. Understanding the mechanisms sustaining a proinflammatory and profibrotic state may offer the potential for targeted pharmacological interventions. This, in turn, could pave the way for combination therapies capable of reversing renal damage in CKD. The non-replacement phase of CKD currently faces a dearth of efficacious therapeutic options. Future directions encompass exploring vaptans as diuretics to inhibit water absorption, investigating antifibrotic agents, antioxidants, and exploring regenerative treatment modalities, such as stem cell therapy and novel probiotics. Moreover, this review identifies pharmaceutical agents capable of mitigating renal parenchymal damage attributed to CKD, targeting molecular-level signaling pathways (TGF-β, Smad, and Nrf2) that predominate in the inflammatory processes of renal fibrogenic cells.
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