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Drug Distribution: Plasma Protein Binding01:29

Drug Distribution: Plasma Protein Binding

Drugs predominantly attach to plasma proteins, with only a small percentage remaining unbound. The unbound portion can be calculated as one minus the bound fraction. Acidic drugs form large, inactive complexes by reversibly binding to plasma albumin, which prevents them from diffusing across biological barriers. These drug-protein complexes act as reservoirs for the drugs. As the concentration of unbound drugs decreases, these complexes quickly dissociate to release the free drug, maintaining...
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Local Anesthetics: Pharmacokinetics01:13

Local Anesthetics: Pharmacokinetics

The potency and duration of action of local anesthetics (LAs) are determined by their pharmacokinetics. Pharmacokinetics describes how LAs are absorbed, distributed, metabolized, and eliminated from the body. When administered to the vascular tissues, LAs are quickly absorbed and enter the systemic circulation, reducing their localized effects. Adding vasoconstrictors such as epinephrine to LAs reduces their absorption into the systemic circulation, making them clinically effective. The...
Local Anesthetics: Mechanism of Action01:23

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Local Anesthetics: Adverse Effects01:12

Local Anesthetics: Adverse Effects

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High-Density Lipoprotein-Specific Phospholipid Efflux Assay
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Plasma Lp-PLA(2) mass and apoB-lipoproteins that carry Lp-PLA(2) decrease after sodium.

Alexander Constantinides1, Michiel N Kerstens, Bert D Dikkeschei

  • 1Department of Endocrinology, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands.

European Journal of Clinical Investigation
|September 11, 2012
PubMed
Summary

A short-term sodium challenge significantly reduced lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) mass and apolipoprotein B-lipoprotein-associated phospholipase A(2) (apoB-Lp-PLA(2)) levels. This suggests a potential dietary intervention for cardiovascular risk markers.

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Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
06:47

Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation

Published on: January 28, 2021

Area of Science:

  • Cardiovascular Disease Research
  • Lipid Metabolism Studies
  • Nutritional Science

Background:

  • Lipoprotein-associated phospholipase A(2) (Lp-PLA(2)) is a key cardiovascular risk marker.
  • Lp-PLA(2) is primarily associated with apolipoprotein B (apoB)-containing lipoproteins.
  • Dietary sodium intake may influence apoB-lipoprotein levels.

Purpose of the Study:

  • To investigate the effect of a sodium challenge on plasma Lp-PLA(2) mass.
  • To determine if a sodium challenge alters apoB-lipoprotein particles carrying Lp-PLA(2) (apoB-Lp-PLA(2)).

Main Methods:

  • A 3-day oral sodium chloride challenge (9 g/day) was administered to 76 participants (45 women, 31 men).
  • Plasma Lp-PLA(2) mass was measured using turbidimetric immunoassay.
  • Levels of apoB-Lp-PLA(2) were assessed using a newly developed enzyme-linked immunosorbent assay.

Main Results:

  • Sodium loading significantly increased urinary sodium excretion.
  • Plasma Lp-PLA(2) mass and apoB-Lp-PLA(2) levels showed significant decreases post-challenge.
  • Associated reductions were observed in total cholesterol, non-HDL cholesterol, LDL cholesterol, apoB, and total cholesterol/HDL cholesterol ratio.

Conclusions:

  • Short-term oral sodium intake effectively reduces both plasma Lp-PLA(2) mass and apoB-Lp-PLA(2) levels.
  • These findings highlight a potential dietary strategy for managing cardiovascular risk markers.