Vitamin C (Liposomal) vs Vitamin D3

Mechanism

Ascorbic acid is an essential electron donor and cofactor for numerous enzymatic reactions. It is required for collagen synthesis (prolyl and lysyl hydroxylases), carnitine biosynthesis, catecholamine synthesis (dopamine beta-hydroxylase), and alpha-ketoglutarate-dependent dioxygenases including HIF-prolyl hydroxylases and TET methylcytosine dioxygenases (epigenetic regulation). It regenerates oxidized vitamin E, supports immune function via neutrophil chemotaxis, phagocytosis, and lymphocyte proliferation. Liposomal delivery bypasses SVCT1/2 transporter saturation, achieving plasma levels closer to IV administration.

Standard Dosing

1000-2000mg liposomal vitamin C daily

Timing

Divided doses throughout the day (every 4-6 hours) for optimal plasma levels. Away from high-dose minerals.

Cycle Duration

ongoing

Side Effects

• Diarrhea/GI upset at high non-liposomal doses (bowel tolerance)
• Kidney stone risk (oxalate pathway)
• False blood sugar readings on glucometers
• Dental erosion (chewable forms)

Contraindications

• Hemochromatosis (enhances iron absorption)
• G6PD deficiency (high-dose IV can cause hemolytic anemia)
• History of calcium oxalate kidney stones (may increase oxalate at high oral doses)
• Renal insufficiency (accumulation risk)

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Mechanism

Vitamin D3 (cholecalciferol) is hydroxylated in the liver to 25(OH)D (calcidiol), then in the kidneys to 1,25(OH)2D (calcitriol), the active hormone. Calcitriol binds the nuclear vitamin D receptor (VDR), forming a heterodimer with RXR that regulates >1000 genes. Key actions: upregulation of intestinal calcium/phosphorus absorption (TRPV6, calbindin), modulation of innate immunity (cathelicidin LL-37 antimicrobial peptide production), suppression of adaptive immune overactivation (Th1/Th17 to Treg shift), regulation of PTH and osteocalcin for bone mineralization, and modulation of insulin secretion from beta cells.

Standard Dosing

5000 IU daily (125 mcg)

Timing

With largest fat-containing meal of the day (fat-soluble). Morning preferred.

Cycle Duration

ongoing (lifelong for most people in northern latitudes)

Side Effects

• Hypercalcemia at excessive doses (>10,000 IU/day long-term without monitoring)
• Nausea/vomiting (toxicity)
• Kidney stones (with excessive calcium)
• Metallic taste (toxicity sign)

Contraindications

• Hypercalcemia
• Granulomatous diseases (sarcoidosis, some lymphomas — unregulated 1-alpha hydroxylase conversion)
• Primary hyperparathyroidism (without monitoring)
• Williams syndrome

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