Verapamil and digoxin are frequently used in combination, and clinical experience suggests that verapamil may increase digoxin toxicity. We have investigated the influence of verapamil on digoxin pharmacokinetics in the rat. Rats were injected with 10 mg/kg verapamil s.c. twice a day for 7 days while control rats were injected with saline only. On the 7th day, all the rats received 0.5 mg/kg of digoxin i.p. Two, 4, 6, 8 and 10 hours later, groups of 6 to 8 verapamil pretreated and control animals were sacrificed and plasma, heart, brain, liver, kidney and muscle digoxin concentrations were assayed. Digoxin levels were significantly higher in the plasma, heart, liver and muscle of the verapamil pretreated rats at 6, 8 and 10 hours (p less than 0.01).

Download full-text PDF

Source

Publication Analysis

Top Keywords

verapamil digoxin
8
rats injected
8
verapamil pretreated
8
plasma heart
8
digoxin
7
verapamil
7
plasma tissue
4
tissue levels
4
levels digoxin
4
digoxin rat
4

Similar Publications

Gastrointestinal absorption and its regulation of hawthorn leaves flavonoids.

Sci Rep

January 2025

School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai, 201203, P.R. China.

Hawthorn leave flavonoids (HLF) are widely used as an herb or dietary supplements for cardio-cerebrovascular diseases. However, its gastrointestinal absorption behavior and mechanism have not been disclosed. In this study, gastrointestinal absorption and its regulation of 4''-O-glucosylvitexin (GLV), 2''-O-rhamnosylvitexin (RHV), vitexin (VIT), rutin (RUT) and hyperoside (HP) in HLF were investigated using in vitro, in situ and in vivo models.

View Article and Find Full Text PDF

Background: Preventing high heart rates in patients with atrial fibrillation (AF) is a key objective of AF management. Data regarding heart rates in patients with paroxysmal AF (PAF) is lacking. This analysis aimed to provide insight into heart rates during PAF episodes measured with continuous implantable loop monitoring.

View Article and Find Full Text PDF

Background: Atrial fibrillation (AF) is associated with an increased risk of hospital admission, but few data on reasons for hospitalization and on the role of anti-arrhythmic drugs are available.

Objectives: The purpose of this study was to investigate the incidence rate and factors associated with all-cause, cardiovascular, and AF-related hospitalizations.

Methods: Prospective ongoing ATHERO-AF (Atherosclerosis in Atrial Fibrillation) cohort study enrolling AF patients on oral anticoagulants.

View Article and Find Full Text PDF

Brigatinib is an oral anaplastic lymphoma kinase (ALK) inhibitor approved for the treatment of ALK-positive metastatic non-small cell lung cancer. In vitro studies indicated that brigatinib is primarily metabolized by CYP2C8 and CYP3A4 and inhibits P-gp, BCRP, OCT1, MATE1, and MATE2K. Clinical drug-drug interaction (DDI) studies with the strong CYP3A inhibitor itraconazole or the strong CYP3A inducer rifampin demonstrated that CYP3A-mediated metabolism was the primary contributor to overall brigatinib clearance in humans.

View Article and Find Full Text PDF
Article Synopsis
  • The study examined the relationship between chronic obstructive pulmonary disease (COPD) and atrial fibrillation (AF) using data from the global GLORIA-AF registry, focusing on how COPD affects treatment and outcomes.
  • Out of 36,263 patients, 6.2% had COPD, with varying prevalence in different regions; factors like age, gender, and smoking were linked to COPD presence.
  • COPD patients experienced different medication patterns and significantly worse health outcomes, including higher risks of death, major adverse cardiovascular events (MACEs), and major bleeding compared to patients without COPD.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!