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Idealized Beauty:
Ancient Greek art, especially in the Hellenistic period, idealized figures like Alexander the Great with wavy hair, a straight nose, and a strong jawline, symbolizing beauty and virtue. Baron shares similar features, reflecting this classical ideal. -
Cultural Aesthetics:
Certain facial structures and hairstyles, associated with leadership and nobility, have remained consistent over time. Baron’s hairstyle mirrors the flowing look of Greek leaders, reflecting enduring beauty standards in modern grooming. -
Anatomical Similarities:
Both figures share symmetrical proportions, like high cheekbones and defined jaws. These features, prized in antiquity, still align with modern perceptions of beauty.
You get it. Try thinking out of our collective lense and steelman the other side. They believe that climate change is real. So, being able to flip the idea around would turn the point invalid.
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Point from our perspective: You believe humans can change the climate, so they can change the weather.
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flipped point from them: You believe humans can change the weather so they can change the climate.
Essentially, rending the point invalid.
Great. Even if you aren't sure of the si,e of the liposome it should still be better than nothing. Could you point me to the brand? Some brands add oil and call it liposomal even though it's not truly a liposomal formulation.
I am glad you got the liposomal form. Do you know its scale?
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The most bioavailable form of lysine is L-lysine hydrochloride (L-lysine HCl). This is the salt form of lysine, The absolute bioavailability of L-lysine hydrochloride (L-lysine HCl) likely around 50-60%
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Liposomal forms of nutrients, including lysine, are designed to improve bioavailability by encapsulating the active compound (in this case, lysine) within lipid bilayers. This liposomal delivery system protects lysine from degradation in the gastrointestinal tract and enhances its absorption through the gut lining.
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Size Matters the size of the liposomes plays a crucial role in determining their absorption efficiency. Research indicates that liposomes right around 100 nanometers (nm) tend to have the best absorption profiles.
It’s perplexing to me that atheist materialists still hold their position, given the overwhelming evidence pointing to the existence of more than just matter in motion.
Consider this simple thought experiment: if the universe – including space, time, matter, and energy – ceased to exist, would the universe itself still exist? The clear answer is "no." Yet, even in this hypothetical absence of the universe, fundamental principles of logic, such as the law of non-contradiction, would still hold true. This suggests that logic is not merely a property of the universe but something that transcends it. If the universe operates according to logical principles that exist beyond it, then it stands to reason that something beyond the material realm governs these truths, pointing to a reality deeper than physical matter alone.
Quercetin and curcumin have complementary rather than directly competitive. You are correct in that both are polyphenolic compounds with strong antioxidant and anti-inflammatory properties, but they target different molecular pathways, allowing for potential synergistic effects.
- Quercetin: Acts primarily through inhibition of pathways like NF-κB, PI3K/Akt, and JAK/STAT, and modulates various enzymes like COX and LOX, contributing to anti-inflammatory and anti-cancer properties.
- Curcumin: Primarily targets NF-κB, STAT3, and MAPK pathways and also inhibits various kinases and transcription factors.
While both affect NF-κB signaling, their precise binding sites and interactions with cellular components differ, so they do not directly compete but may enhance each other's effects, particularly in cancer research where their combination is studied for enhanced anti-angiogenesis and apoptosis-inducing activities.
Below is a more comprehensive breakdown of the Pharmacodynamic Properties of Quercetin and Curcumin
Quercetin Pharmacodynamics
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Antioxidant Activity:
- Quercetin is a potent scavenger of free radicals, reducing oxidative stress by neutralizing reactive oxygen species (ROS). It also upregulates endogenous antioxidant enzymes like superoxide dismutase (SOD), catalase, and glutathione peroxidase.
- Mechanism: Direct scavenging of radicals and inhibition of xanthine oxidase, which produces superoxide radicals.
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Anti-inflammatory Activity:
- Quercetin inhibits pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) by blocking the NF-κB pathway. It also downregulates enzymes like COX-2 and 5-LOX, reducing prostaglandins and leukotrienes.
- Mechanism: Suppression of NF-κB activation and inhibition of MAPKs (mitogen-activated protein kinases), leading to reduced expression of inflammatory genes.
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Anti-cancer Effects:
- Quercetin induces apoptosis and inhibits proliferation in cancer cells. It works by modulating the PI3K/Akt/mTOR and JAK/STAT pathways, both involved in cell growth and survival.
- Mechanism: Activation of pro-apoptotic proteins (Bax, caspases) and inhibition of anti-apoptotic proteins (Bcl-2). It also disrupts the cell cycle by regulating cyclins and CDKs (cyclin-dependent kinases).
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Angiogenesis Inhibition:
- Quercetin inhibits angiogenesis, the formation of new blood vessels, a crucial process in tumor growth.
- Mechanism: Downregulation of VEGF (vascular endothelial growth factor) and suppression of HIF-1α (hypoxia-inducible factor 1-alpha), limiting the blood supply to tumors.
Curcumin Pharmacodynamics
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Antioxidant Activity:
- Curcumin is also a strong antioxidant, directly scavenging ROS and upregulating antioxidant enzymes like glutathione. Curcumin’s antioxidant effects are closely linked to its anti-inflammatory and anti-cancer properties.
- Mechanism: Direct scavenging and upregulation of Nrf2 (nuclear factor erythroid 2-related factor 2), a transcription factor that controls the expression of antioxidant proteins.
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Anti-inflammatory Activity:
- Curcumin inhibits inflammatory mediators like TNF-α, IL-6, and IL-1β, primarily through the NF-κB pathway but also via STAT3 inhibition. It reduces the expression of COX-2 and LOX, much like quercetin.
- Mechanism: Suppression of NF-κB and STAT3, which reduces the transcription of inflammatory genes.
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Anti-cancer Effects:
- Curcumin exerts its anti-cancer effects through multiple pathways, including apoptosis induction, inhibition of cell proliferation, and suppression of metastasis. It targets the PI3K/Akt and mTOR pathways, similar to quercetin, but also impacts Wnt/β-catenin signaling, making it effective in various cancer types.
- Mechanism: Curcumin inhibits cyclin D1, CDKs, and promotes pro-apoptotic factors like p53 and caspases. It also inhibits metastasis by downregulating matrix metalloproteinases (MMPs) and modulating epithelial-to-mesenchymal transition (EMT).
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Angiogenesis Inhibition:
- Curcumin blocks angiogenesis, particularly in the context of tumor growth. It does this by inhibiting VEGF, FGF (fibroblast growth factor), and PDGF (platelet-derived growth factor).
- Mechanism: Curcumin reduces HIF-1α and VEGF expression, similar to quercetin, but also inhibits other pro-angiogenic factors like MMP-9 and angiopoietins.
Potential Synergy in Pharmacodynamics
Although both compounds have overlapping actions (e.g., inhibiting NF-κB, VEGF, and inducing apoptosis), they do not directly compete in their mechanisms. Instead, they complement each other by targeting different aspects of similar pathways or working on parallel pathways that converge at key points:
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Complementary Antioxidant Effects:
- Both quercetin and curcumin reduce oxidative stress but through slightly different mechanisms. Quercetin’s direct scavenging and enzyme inhibition (e.g., xanthine oxidase) combined with curcumin’s activation of the Nrf2 pathway provide a broader antioxidant defense.
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Enhanced Anti-inflammatory Action:
- Quercetin’s inhibition of PI3K/Akt and JAK/STAT complements curcumin’s STAT3 suppression and NF-κB inhibition, resulting in a stronger reduction of inflammatory mediators like TNF-α and IL-6.
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Dual Targeting of Apoptosis and Cell Proliferation:
- Quercetin primarily acts through Bax/Bcl-2 modulation, while curcumin also engages p53 and cyclin pathways. This allows for enhanced apoptosis and inhibition of cancer cell proliferation from multiple angles.
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Stronger Angiogenesis Inhibition:
- Both quercetin and curcumin inhibit VEGF and HIF-1α, but curcumin also suppresses FGF and PDGF, which are critical in cancer-induced angiogenesis. Together, they provide a more comprehensive blockade of blood vessel formation in tumors.
Pathways of Interest in Cancer Research
- NF-κB: Both quercetin and curcumin inhibit NF-κB, leading to reduced inflammation, decreased cancer cell proliferation, and inhibition of survival signals.
- PI3K/Akt/mTOR: Quercetin and curcumin both target this pathway, which is crucial for cell growth and survival, particularly in cancer cells.
- JAK/STAT: Quercetin's effects on JAK/STAT could complement curcumin’s suppression of STAT3, enhancing their combined anti-inflammatory and anti-cancer effects.
- VEGF/HIF-1α: Their combined suppression of VEGF and HIF-1α, critical regulators of angiogenesis, is particularly important for limiting tumor growth.
Sources:
Not exactly. Although i would reccomend a low carb low FODMAP diet, fenbendazole inhibits glycolysis which mitigates much of the fuel the cancer is getting (generally) and it inhibits P-gp pumps.