Why a hot cuppa is better for you than you think:

Sure, there is the addictive caffeine, and the tea stains, but imagine that caffeine megalomania of coffee toned down by the ingredients of L-theanine, a psychoactive and immunoactive ingredient. So when you see your workers or colleagues drinking tea, it is so that they are more efficient, focused, and mentally stable. I once worked with a high-strung man who claimed that all I did was sit around and drink tea. Well dude, if it wasn't for me drinking tea all day, making the molecular lab from scratch thanks to the good doctor, you wouldn't be working there to complain about everything.

Black tea and L-theanine.

Anti-proliferative effect of ascorbic acid

This is a fascinating paper. Of course, one should read it and see the methods and dosage.

Belin et. al

Hyperhomocysteinemia, Hyperglycemia, Hypertension, Oxidative Stress, and Inflammation = Atherosclerosis

Given that pathological changes to the liver cause a reduction in plasma LDL and Lp(a), it doesn't necessarily follow that cholesterol is a causal factor in pathological conditions. Especially if an individual has normal cholesterol metabolism, and isn't shoveling in excessive canisters of saturated fats (paraffins/waxes) and hydrogenated oils (gasoline) into their mouths, plasma cholesterol (HDL, LDL, ILDL, VLDLDL, Lp(a) are responses to other conditions. Something that is often misunderstood is that there are many kinds of fat, only one cholesterol, free cholesterol, esterified cholesterol, and several lipoproteins that include cholesterol. Cholesterol on its own is not water soluble. Cholesterol can only travel through the blood if part of a protein or polar lipid shuttle, such as that constituted by lipoproteins. LDL then is NOT cholesterol, but ApoB protein and cholesterol which serves to shuttle cholesterol through the blood to where it is supposed to go. These proteins, ApoA, ApoB, ApoE, ApoJ, Apo(a), etc. are not just randomly secreted by the liver. They are made for a purpose under the control of a homeostat protein. Just as rusted (oxidized) or rotten food can poison someone, so can rusted or rotten lipoprotein (oxidized LDL, ox-LDL, ox-phospholipid, nitrated, glycated, chlorinated, denatured lipid/lipoprotein) poison the repair system of the artery. This poison dump causes a local immune system reaction to attempt to clear out the junk yard. Yet, each soldier (white blood cell) that comes to the site gets poisoned and dies there in the graveyard (foam cell lesion that becomes necrotic core). This graveyard then gets bigger and bigger, until it is finally the atherosclerotic lesion.

It is true that it is associated with pathological conditions, and that hereditary hypercholesterolemia and build up syndromes cause disease. It is also true that some individuals have a genetic predisposition to higher Lp(a) or LDL levels. Yet, it is also true that natural and ubiquitous hormones such as testosterone and naturally produced and occurring antioxidants such as CoQ(10) can dramatically lower this "harmful" cholesterol.

So then, without a person inhaling several burgers, a grocery bag of trans-fat fries, and an entire gallon of whole milk ice-cream a day, what is it?

The Worldwide Model for Cardiovascular Medicine:

1) The ApoE KO mouse.
2) The LDL receptor KO mouse.
(sometimes they use salt hypertensive or STZ diabetic models)

None of these have apo(a) as humans do, and all create ascorbate within their own livers which humans don't do. Another thing to keep in mind is that mice eat 1/4 their own weight ( ! ) in food a day. For a 150 pound human, that is nearly 38 pounds of food a day. This doesn't reduce the validity of the model, but people generally ignore some profound differences between mouse and man. This mouse model is the main pillar of all of cardiovascular medicine for humans.

The Comedy of Academic Journals:

I have been published in various places already, but here is my recent experience in the field of cardiovascular medicine:

There is no cure for Aortic Aneurysm. No surgical intervention works very long, in fact this is what the famous Dr. DeBakey (DeBaghi) died of.

My first reviewer had some valid requests, but we can't do it because we have other things to do and other people have already proven what they ask for. They also ask to prove a parameter through a litmus test, when the evidence for it is right in front of them in another form.

The second reviewer obviously didn't even read the paper. They claim that I claim that the plaques resolve themselves, which is never stated anywhere within the paper. They are either asleep at the wheel or yet another pawn of scientific disinformation. The other absurd thing they request is "citations" for a novel find.

Oh well. Dr. DeBakey is turning in his grave. If I had to, I would just put the paper online and claim, "All of it is true, but there are no peer reviewers."

Here it is, and I am the first to state it ever in the world: In Mice, Aortic Dissections heal themselves often, but they do not in humans. Whoever claims it again basically owes me credit for the assertion of the whole chain of discovery. ha!

As history has shown, the ancient pillars of science are not infallible, and no human is infallible in their assertions. The gloss or prestige of a journal is only so important as to have power, but there are plenty of retractions and corrections in high profile science.

Vitamin C as a Cancer Target (From Wikipedia)

A biologist knows what a LOF mutation is and induces these to study what a gene function is. In the case of natural mutants of the VHF gene, these patients are very prone to cancer disease partially by constitutive activation of HIF. By adding elements (of which vitamin C is one), this process could be reversed:

"Treatment

Suggested targets for VHL-related cancers include targets of the HIF pathway, such as VEGF. Two inhibitors of VEGF sorafenib and sunitinib have recently been approved by the FDA [6]. The mTOR inhibitor rapamycin may also be an option [9]. Bevacizumab, a monoclonal antibody targeting VEGF, is one medication currently undergoing clinical trials

Since iron, 2-oxoglutarate and oxygen are necessary for the inactivation of HIF, it has been theorized that a lack of these cofactors could reduce the ability of hydroxlases in inactivating HIF. A recent study has shown that in cells with a high activation of HIF even in oxygenated environments was reversed by supplying the cells with ascorbate [10]. Thus, Vitamin C may be a potential treatment for HIF induced tumors." (as of 3/25/09) reference 10 being:

^ Knowles HJ, Raval RR, Harris AL, Ratcliffe, PJ. (2003). "Effect of ascorbate on the activity of hypoxia-inducible factor in cancer cells.". Cancer research 63: 1764–8.

Here is the Wikipedia link showing the value of vitamin C as a therapeutic against cancer: http://en.wikipedia.org/wiki/Von_Hippel-Lindau_tumor_suppressor link

Tea Benefits:

(wikipedia entry:)

Tea Boosts