Related Experiment Video
Updated: Jul 16, 2026

08:09
A Doxorubicin-induced Cardiomyopathy Model in Adult Zebrafish
Published on: June 7, 2018
[Chronic drug-induced hepatitis caused by dihydralazine].
G Roschlau1, S Hass, V Schmehl
1Pathologischen Institut, St. Hedwigs-Krankenhauses, Berlin.
Summary
Dihydralazine can cause chronic aggressive hepatitis, even without symptoms. Early detection of elevated transaminases and drug withdrawal leads to recovery, highlighting the importance of liver monitoring.
Area of Science:
- Hepatology
- Clinical Pharmacology
- Toxicology
Background:
- Dihydralazine is a vasodilator used in hypertension treatment.
- Drug-induced liver injury (DILI) is a significant clinical concern.
- Chronic aggressive hepatitis can be a manifestation of DILI.
Observation:
- Two cases of dihydralazine-induced chronic aggressive hepatitis are presented.
- One patient presented with obstructive jaundice, while the other was asymptomatic with elevated transaminases.
- Exposure to dihydralazine ranged from 2-3 years.
Findings:
- Biopsy confirmed chronic aggressive hepatitis in both cases.
- Withdrawal of dihydralazine resulted in patient recovery within 2-3 months.
- Acute dihydralazine-hepatitis was more frequent (77:2 ratio) than chronic cases in a review of 6,581 liver biopsies.
Implications:
- Elevated transaminases warrant drug withdrawal or liver biopsy to rule out dihydralazine hepatotoxicity.
- This study underscores the potential for dihydralazine to cause severe liver injury.
- Awareness of dihydralazine's hepatotoxic potential is crucial for clinicians managing hypertensive patients.
Related Concept Videos
Antihypertensive Drugs: Action of Diuretics
Diuretics are antihypertensive drugs used to treat hypertension resulting from sodium and water retention. Sodium, vital for fluid balance and nerve or muscle function, is regulated by the kidneys through millions of nephrons. Blood enters nephrons via afferent arterioles, which branch into capillaries called glomeruli. These filter blood plasma, allowing water and solutes, like sodium ions, to pass through capillary walls into Bowman's capsule. The filtrate then flows through various tubules...
Antihypertensive Drugs: Thiazide-Class Diuretics
Thiazide diuretics are sulfonamide derivatives featuring a benzothiadiazine ring system in their molecular structure. Based on this structure, thiazide diuretics can be categorized into two groups: thiazide-type and thiazide-like diuretics. Thiazide-type diuretics, including hydrochlorothiazide and chlorothiazide, consist of a benzothiadiazine backbone with an attached sulfonamide group. Thiazide-like diuretics, such as chlorthalidone and indapamide, lack the thiazide ring but demonstrate...
Heart Failure Drugs: Diuretics
Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
Chronic liver disease significantly impacts drug metabolism due to alterations in hepatic blood flow and enzyme accessibility. This disruption affects the body's pharmacokinetics—the movement and processing of drugs within the system. Key enzymes crucial for metabolizing medications become less accessible, changing how drugs are processed and utilized. Furthermore, liver disease influences the synthesis of plasma proteins, such as albumin and globulins, which play critical roles in drug binding...
Drug toxicity: Idiosyncratic Reactions
Idiosyncratic drug reactions represent abnormal chemical responses that vary significantly among individuals, ranging from extreme sensitivity to low doses to insensitivity to high doses. These reactions often occur due to the drug's covalent binding with serum proteins, forming a foreign hapten that triggers an immunotoxicological response. The variability in drug reactions has a strong pharmacogenetic foundation, with genetic differences crucial in how individuals metabolize drugs. For...
Rheumatic Heart Disease I: Introduction
Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...

