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Related Concept Videos

Overview of Protein Metabolism01:21

Overview of Protein Metabolism

Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
Pharmacokinetics: Drug–Drug Interactions01:25

Pharmacokinetics: Drug–Drug Interactions

Drug interactions occur when the pharmacological effect of one drug is altered by another substance, either enhancing or diminishing its activity. The drug whose activity is altered is known as the object drug, and the substance causing the alteration is called the agent drug or the precipitant. The net effects of these interactions are mostly undesirable, leading to decreased effectiveness or increased adverse effects. In rare cases, interactions can be beneficial, such as the enhanced...
Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion01:20

Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion

Drug metabolism, a critical process in the liver, involves two primary phases: Phase I reactions and Phase II conjugation. Obesity introduces significant alterations in this metabolic process, primarily due to fatty infiltration of the liver, leading to conditions such as nonalcoholic fatty liver disease (NAFLD). This condition can modify the activities of both Phase I and II enzymes, impacting how drugs are metabolized in obese patients.Phase I metabolism sees variable effects across...
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase01:27

Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase

Phase II biotransformation reactions are essential for detoxifying and eliminating xenobiotics, including many pharmaceutical compounds. These reactions typically involve conjugation, the covalent attachment of polar endogenous groups such as glucuronic acid, sulfate, methyl, or acetyl moieties to functional groups introduced during Phase I metabolism. The resulting conjugates are more water-soluble, enabling efficient renal or biliary excretion.The major classes of Phase II enzymes include...
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Related Experiment Video

Updated: Jul 14, 2026

Cellular Redox Profiling Using High-content Microscopy
11:37

Cellular Redox Profiling Using High-content Microscopy

Published on: May 14, 2017

Metabolic issues associated with protease inhibitors.

Graeme Moyle1

  • 1HIV Medicine, St. Stephens Centre, Chelsea and Westminster Hospital, London, United Kingdom. gm@moyleg.demon.co.uk

Journal of Acquired Immune Deficiency Syndromes (1999)
|May 26, 2007
PubMed
Summary

HIV infection and antiretroviral therapy (ART) cause metabolic changes, increasing cardiovascular disease risk. Management involves lifestyle changes, medication, and careful drug selection to mitigate these risks.

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Area of Science:

  • Cardiology
  • Endocrinology
  • Infectious Diseases

Background:

  • HIV infection is associated with dyslipidemia, including low HDL and high triglycerides.
  • Antiretroviral therapy (ART) can exacerbate metabolic issues, increasing LDL, VLDL, triglycerides, and insulin resistance.
  • These metabolic changes elevate cardiovascular disease (CVD) risk in HIV-positive individuals.

Purpose of the Study:

  • To highlight the metabolic and cardiovascular risks associated with HIV and ART.
  • To emphasize the limitations of standard risk calculators in this population.
  • To discuss management strategies for metabolic risk in HIV-positive patients.

Main Methods:

  • Review of metabolic alterations in HIV infection.
  • Analysis of ART's impact on lipid profiles and insulin sensitivity.
  • Evaluation of cardiovascular risk assessment in the context of HIV.

Main Results:

  • HIV and ART contribute to dyslipidemia and insulin resistance.
  • Cardiovascular risk may be underestimated by conventional calculators.
  • Metabolic complications pose a significant CVD risk.

Conclusions:

  • HIV-positive individuals face elevated CVD risk due to metabolic changes from infection and ART.
  • Management requires lifestyle interventions, pharmacotherapy, and judicious ART selection.
  • Personalized strategies are crucial for mitigating metabolic and cardiovascular risks.