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Related Concept Videos

Effect of Hepatic Disease on Pharmacokinetics: Active Drug, Metabolite and Fraction of Metabolized Drug01:14

Effect of Hepatic Disease on Pharmacokinetics: Active Drug, Metabolite and Fraction of Metabolized Drug

In pharmacotherapy, monitoring drug concentrations is paramount, especially for drugs whose therapeutic effects hinge on both the active compound and its metabolite. Hepatic impairment profoundly influences drug potency by altering liver function. If the drug is more potent than its metabolite, impaired liver function amplifies drug activity due to elevated drug concentration levels. Conversely, if the metabolite holds greater potency, diminished liver function diminishes drug activity by...
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test01:22

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess the...
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow01:26

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...
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
Diseases of the Liver and Gallbladder01:26

Diseases of the Liver and Gallbladder

Liver and gallbladder diseases are a significant health concern, with prominent conditions including cirrhosis, hepatitis, non-alcoholic fatty liver disease (NAFLD), and gallstones. Jaundice is a common manifestation of liver and biliary disease.
Cirrhosis is characterized by the scarring of hepatic lobules in the liver, which are replaced by fibrous tissue, affecting the liver's normal functioning. NAFLD, on the other hand, is caused by an excessive build-up of fat in the liver, not related to...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...

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Related Experiment Videos

Silybin and the liver: from basic research to clinical practice.

Carmela Loguercio1, Davide Festi

  • 1Gastroenterology School-Interuniversity Research Centre on Foods, Nutrition and Gastrointestinal Tract (CIRANAD), 2nd University of Naples, 80131 Naples, Italy. carmelina.loguercio@unina2.it

World Journal of Gastroenterology
|June 3, 2011
PubMed
Summary

Silybin, derived from milk thistle, shows promise for chronic liver disease. While clinical evidence is still developing, experimental studies confirm its antifibrotic, antioxidant, and metabolic benefits, with good bioavailability and safety.

Keywords:
Hepatic fibrosisHepatic inflammationLiver diseaseMilk thistleRadical speciesSilymarin

Related Experiment Videos

Area of Science:

  • Hepatology
  • Pharmacology
  • Natural Products

Background:

  • Herbal products, including milk thistle extracts like silymarin and silybin, are frequently used for chronic liver disease.
  • The clinical efficacy of these natural compounds remains under investigation, necessitating further research.

Purpose of the Study:

  • To review existing literature on the effects of purified silybin (free and conjugated) on liver cells, experimental liver damage, and patients with liver disease.
  • To evaluate the antifibrotic, anti-inflammatory, antioxidant, and metabolic properties of silybin.

Main Methods:

  • A comprehensive literature search of PUBMED was conducted for in vitro and in vivo studies on silybin.
  • The review incorporated experimental data and clinical trial information, alongside expert knowledge.

Main Results:

  • Silybin phytosome exhibits higher bioavailability than silymarin, with reduced impact from liver damage.
  • Experimental studies confirm silybin's antifibrotic, antioxidant, and metabolic effects.
  • Silybin demonstrates a favorable safety profile with no significant drug interactions at doses below 10 g/d.

Conclusions:

  • While previous human studies were limited, current clinical trials for silybin in chronic liver disease are promising.
  • Silybin presents as a potentially valuable therapeutic agent for managing chronic liver conditions based on current evidence.