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Pharmacology
Systemic Pharmacotherapeutics of the Urinary System
Glomerular Disease
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  • Behavior
  • Circulatory System
  • Clinical Pathology and Procedures
  • Digestive System
  • Emergency Medicine and Critical Care
  • Endocrine System
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Chapters in Pharmacology
  • Pharmacology Introduction
  • Systemic Pharmacotherapeutics of the Cardiovascular System
  • Systemic Pharmacotherapeutics of the Digestive System
  • Systemic Pharmacotherapeutics of the Eye
  • Systemic Pharmacotherapeutics of the Integumentary System
  • Systemic Pharmacotherapeutics of the Muscular System
  • Systemic Pharmacotherapeutics of the Nervous System
  • Systemic Pharmacotherapeutics of the Reproductive System
  • Systemic Pharmacotherapeutics of the Respiratory System
  • Systemic Pharmacotherapeutics of the Urinary System
  • Chemotherapeutics Introduction
  • Anthelmintics
  • Antibacterial Agents
  • Antifungal Agents
  • Anti-Inflammatory Agents
  • Antineoplastic Agents
  • Antiseptics and Disinfectants
  • Antiviral Agents and Biologic Response Modifiers
  • Ectoparasiticides
  • Growth Promotants and Production Enhancers
  • Vaccines and Immunotherapy
Topics in Systemic Pharmacotherapeutics of the Urinary System
  • Overview of Systemic Pharmacotherapeutics of the Urinary System
  • Bacterial Urinary Tract Infections
  • Fungal Urinary Tract Infections
  • Diuretics
  • Dopamine in Urinary Disease
  • Glomerular Disease
  • Diabetes Insipidus
  • Controlling Urine pH
  • Cystine-binding Agents in Urinary Disease
  • Urinary Incontinence
  • Urine Retention
 
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Glomerular Disease

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Angiotensin-converting enzyme (ACE) inhibitors may be beneficial in the management of dogs and cats with chronic renal failure (CRF). Renal disease progresses to CRF as a consequence of functional adaptations of the remaining nephrons, including glomerular hyperperfusion and hypertension controlled by angiotensin II. These responses initially enhance nephron filtration capacity and compensate for the decrease of glomerular filtration rate, but are detrimental in the longterm and cause further nephron loss. Administration of ACE inhibitors lowers glomerular pressure by decreasing systemic blood pressure and locally inhibiting angiotensin II. In CRF patients, ACE inhibitors may decrease proteinuria caused by changes in glomerular membrane permeability and selectivity from mechanical injury induced by glomerular hypertension, potentially slowing disease progression. ACE inhibitors also tend to increase appetite and body weight in renal failure patients. Enalapril is used in dogs at a dosage of 0.5 mg/kg, PO, sid-bid; benazepril is used in cats at a dosage of 0.5–1.0 mg/kg, PO, sid.

Dimethyl sulfoxide has been used in dogs with amyloidosis with variable results. It is given at a dosage of 80 mg/kg/day, divided tid and given as a 10% solution either PO or SC. Thromboembolism and systemic hypertension are frequent complications of glomerular diseases in dogs, and to a lesser extent in cats, and should be managed as the need arises. Thromboembolism may be prevented by giving aspirin at 0.5–5 mg.kg bid, to high-risk animals such as those with serum albumin <2.0 g/dL, plasma fibrinogen >400 mg/dL, or plasma antithrombin III activity <70%.

Last full review/revision March 2012 by Patricia M. Dowling, DVM,MSc, DACVIM, DACVCP

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