HDL3 particles (HDL3-P) are the smallest fully formed HDL particles. Hepatocytes and enterocytes produce the most important protein of HDL, Apo A-1. Apo-A1 collects phospholipids and a small amount of unesterified cholesterol to form a nascent Pre β-1 HDL. The Pre β-1 particles rapidly gather free cholesterol to become fully formed HDL3 particles.
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HDL3 particles (HDL3-P) are the smallest fully formed HDL particles. Hepatocytes and enterocytes produce the most important protein of HDL, Apo A-1. Apo-A1 collects phospholipids and a small amount of unesterified cholesterol to form a nascent Pre β-1 HDL. The Pre β-1 particles rapidly gather free cholesterol to become fully formed HDL3 particles.
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I have previously posted a summary of the “HDL3-P Activation Index” assay and a description of Reverse Cholesterol Transport (RCT) showing HDL3-P as a primary contributor to the RCT process. Additionally, HDL3-P provides anti-inflammatory and antioxidant protection to LDL most likely from paraoxonase-1.
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The observation that small HDL particles (HDL3-P) are produced immediately on the consumption of protein is important in the functionality of HDL. There are many markers known today for CVD risk but, since HDL3-P is the primary player in reverse cholesterol transport (RCT) it has promise as a leader.
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Consumption of protein stimulates, in a time dependent manner, the posprandial production of Apo A1 and HDL3 particle production. This HDL3 particle activation can be measured as the difference between fasting and postprandial specimens.
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A treatment to reduce the inflammation of calcified and micro-calcified plaque by providing an anti-inflammatory response at the exact location of the inflammation. The non-steroid gallium compound treatment incorporates into the lesion and provides anti-inflammatory activity that can last for months
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Scholarly articles suggest that either high or low HDL3-C/HDL3-P is atherogenic creating uncertainty on the functionality of HDL3. Recent articles have also focused on the importance of HDL3 over HDL2 in reverse cholesterol transport (RCT), anti-oxidant and cardioprotective function. HDL3 is usually identified by analytical methods measuring either size or density and two types of HDL3 have been identified with the same size and density.
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Gallium compounds, which are non-steroids, have been studied for various cancer treatments in animals and humans and found to be effective in a number of trials. In fact, the use of gallium nitrate (GN) is FDA approved for the treatment of hypercalcemia (bone calcium loss) in cancer patients. Also, the anti-inflammatory and neuropathic pain blocking properties of gallium compounds have been studied and are relevant to the treatment of TBI.
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