How We're Reversing Alzheimer’s Disease for Our Clients: The Breakthrough Approach!

brenden henry

Published on: 30/10/2024

How We're Reversing Alzheimer’s Disease for Our Clients: The Breakthrough Approach! Hi, Brenden here, and I have a story I want to share with you all today about how we reversed Alzheimer's disease, something most consider impossible. And you know, in some of the videos I make, the claims may sound too good to be true, but the reality is that these are the true stories about the results we're getting for our clients. So, this one guy's mother was dealing with advanced stage Alzheimer's disease, and I know exactly how devastating that can be because my grandma was suffering from it in the past. Now, in this case, it was so severe she couldn't even recognize some of her own family members. She was at the point where she couldn't hold a coherent conversation with them and needed a caregiver 24/7. So, she was in a pretty bad state, right? Now, let me tell you what happened in just one month of being on my prescribed peptide stack, and in fact, she saw improvements in as little as one week. So, she was able to have coherent conversation with her family members for up to four hours, and she recognized them completely. She even called all the members in her family personally and hosted a family reunion, coordinating the entire thing on her own without any help. Just imagine how rewarding that must have been for everybody in the family. I mean, she's much more independent now, and her doctor was, well, he couldn't believe it. I mean, he even called it a miracle, and he said that after he saw her for himself, because reversing late-stage Alzheimer's disease, it's pretty much something that everybody considers to be impossible, you know? Now, in my free course, The Life-Changing Magic of Peptides, I cover one specific peptide that's been proven to help in Alzheimer's, in transgenic mouse models with three mutations that lead to amyloid plaque buildup. This peptide was shown to regrow mushroom spines by 100% and correct metabolic disturbances that contribute to the disease. You can get this free course by clicking the link in the description, or if you want a full consult and personalized program to help your loved one with Alzheimer's, check the other link. But in this video, I want to dive into some new research as of 2024. It goes into what actually drives Alzheimer's disease progression, and the root of it all appears to be impaired glucose metabolism in the brain. Now, it's not that simple, so let me explain. There's an enzyme in the brain called IDO1, and while impaired glucose metabolism is associated with its increase, it's also increased by inflammatory cytokines and oxidative stress, which can occur as part of the senescence-associated secretory phenotype, also known as SASP. And again, impaired glucose metabolism can contribute to this pathology as well. So when this condition develops, IDO1 also increases and converts tryptophan, an amino acid used to produce serotonin, into a harmful metabolite called Kynurenine. And high levels of IDO1 drive dysfunctional astrocytes. Now, you may not know what astrocytes are, but think of them as the quality control of our neurons. Their job is to keep our neurons healthy. But when astrocytes become dysfunctional, as they do in Alzheimer's disease, they starve neurons of energy by reducing lactate transfer from the astrocytes to the neurons. And this leads to impaired cognition and an increase in tau protein tangles and amyloid beta buildup, blocking neurons from communicating properly. Now, this increases oxidative stress and inflammatory cytokines, which further upregulates IDO1, which accelerates the decline in neuron energy availability and cognitive decline. So it is this vicious cycle, which is why people with Alzheimer's disease typically don't improve. They only get worse. So what's the solution? Well, the recent paper I mentioned talks about using an IDO1 inhibitor, which is actually a type of cancer drug that could be repurposed to improve brain glucose homeostasis. Now, they demonstrated that this can improve several aspects of cognition in Alzheimer's disease, and it makes sense. I mean, we have seen that intranasal insulin can improve cognition in Alzheimer's disease, but it's also limited since it has a hard time reaching the hippocampus, which is what's most implicated in Alzheimer's disease. Now, while IDO1 inhibitors and intranasal insulin show some promise, these methods are still light years behind the innovative approaches we've developed for our clients, which have consistently yielded positive results. You see, we were just following proven peptide science, including how certain peptides were able to regrow mushroom spines by 100% in transgenic mice and improve cognition in mice that were given diabetes, and even improve cognition in healthy mice and in healthy humans. So not only does the mechanistic data on these strategies show an inhibition of IDO1 indirectly through multiple mechanisms, but also reducing oxidative stress, boosting neuroprotective factors, increasing the non-amyloidogenic pathway, and reversing senescence of both neurons and the blood vessels to control the virus. While the improved metabolic health, like better glucose regulation, can improve mitochondrial functioning and gene transcription, peptides can also directly stimulate gene expression and decondense chromatin, which puts them a step ahead. So to recap, a major problem in Alzheimer's is impaired glucose metabolism in the brain, and while theories about oxidative stress and dysfunctional astrocytes aren't wrong, they're just components of the problem. After reviewing your loved one's situation, we can provide a specific peptide stack, medication adjustments, and optimizations for lifestyle and nutrition, all uniquely tailored to them. Now in this person that I mentioned at the start of this video, they wanted to avoid injections and nasal sprays, so we put them on an only oral stack, and even that was enough to give the transformation that I described. So it's just amazing guys.

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Secrets of Tadalafil

brenden henry

Published on: 09/10/2024

What if I told you that Cialis, a drug known for its use by elderly men to strengthen their erections, is actually one of the most potent health enhancers for men on the planet? Most guys are embarrassed at the thought of even using it, but Tadalafil, as it's officially called, is not just erectile dysfunction medication. Not only does it help with blood flow for erections, but this ED medication can literally prolong stem cell life, which can give your body the ability to regenerate almost any tissue, even if they normally won't heal. For example, one guy had a foot wound that would not heal for 20 years until he started Tadalafil. Tadalafil is useful for improving the function of the heart after an ischaemic injury such as a heart attack, and has been shown to result in a 13% lower incidence of major cardiovascular events, 25% lower mortality, and 39% lower cardiovascular related mortality compared to a control group in patients who had at least one cardiovascular disease risk factor. Tadalafil also enhances muscle growth and enhances bone strength through its ability to increase testosterone and upregulate androgen receptors. Tadalafil helps to reduce symptoms of benign prostatic hyperplasia by improving the testosterone to estrogen ratio, relaxing smooth muscle in the prostate and bladder, and improving blood flow, which can reduce symptoms like frequent urination and slow urination. Tadalafil can reduce blood pressure and improve endothelial function, thus lowering the risk of cardiovascular disease through regulating endogenous antioxidant production and dilating arteries, which can help prevent a blood clot from forming. Many people take aspirin to help prevent blood clots, and this works by thinning the blood, but the downside to this is that it can increase brain bleeds from trauma. Tadalafil doesn't thin the blood, it just dilates arteries, which could potentially make it a safer option, but it can still cause side effects if you use it incorrectly. So by the end of this video you will learn how to use Tadalafil most effectively, and an incredibly powerful synergistic combination you can use with it to get more healing power. My name is Brenden Henry, the world's leading expert in peptide science. I was the first person to make a video on the incredible power of the vesugen peptide for enhancing the proliferation and differentiation of mesenchymal stem cells and delaying their senescence. This is huge because stem cells cost tens of thousands of dollars, but this peptide can increase your own naturally for a small fraction of the price of stem cell clinics. This can lead to the acceleration of healing in your body. Whether you have an organ that's damaged, a joint, muscle, or recently undergone a surgical procedure, this will help you heal more quickly. And you can get even more benefits out of it by combining it with Tadalafil. This protocol can work well on its own, or it can be used to enhance the effects of stem cells you receive at the clinic. I currently have a client who purchased my peptide mastery course and coaching, link in the description, and he is looking to maximize the potential of a stem cell treatment at the clinic. So this is of course one of the things included in our protocol, and just one example of how traditional medications or supplements can synergize with certain peptides in ways that are not known by the majority of the people on the planet. In this video, I want to talk about what Tadalafil is and how it works on a mechanistic level so that you can understand the benefits it has to offer more clearly and be more willing to confidently use it to enhance yourself. Then I will tell you how to best use it and dose it so that you get all of the benefits without any toxic effects. First, Tadalafil is a PDE5 inhibitor that prevents the breakdown of CGMP, which enhances blood flow by promoting vasodilation. While it doesn't create CGMP directly, which requires nitric oxide, it helps increase CGMP levels by stopping its degradation. However, PDE5 inhibitors have some crosstalk with PDE8, which are high affinity C-AMP specific enzymes, leading to increased nitric oxide production indirectly. This crosstalk is significant because without it, these inhibitors would be much less effective because they'd have less nitric oxide to work with. Tadalafil's attributes extend to stimulating endogenous antioxidant production in muscle cells, cavernous tissue, and lung endothelial cells. This effect is due to hormesis, which is the body's upregulated production of endogenous antioxidants in response to a mild stressor, leading to a net protective effect. Evidence of this is seen in lung endothelial cells, where Tadalafil, by activating the CGMP-PKG1 pathway, enhances cellular antioxidant defenses, protecting against oxidative stress and dose damage. This leads to improved endothelial function in humans. Tadalafil also reduces the risk of thromboembolism, which is blood clots in males. Getting further into the mechanistic data, PDE5 inhibition increases CGMP levels, which stimulates PKG1 and also leads to an increase in androgens. PKG1 and PKG2 mediate the effects of CGMP, and Leydig cells express mRNA for both. However, inhibiting PKG leads to a dose-dependent decrease in androgen production, indicating that PKG is necessary for the CGMP-driven rise in androgens. When Tadalafil activates CGMP-PKG1, it phosphorylates the star protein, enhancing the transport of cholesterol into mitochondria and increasing testosterone production in Leydig cells. PDE5 inhibitors also interact with PDE8, leading to an intracellular C-AMP increase in Leydig cells, further facilitating testosterone production. Mice with PDE8 knockout have up to 4x more testosterone. Tadalafil has been shown to increase testosterone levels by an impressive 40% in men with metabolic syndrome over time. In a direct comparison with Sildenafil, Tadalafil has been found to be superior at increasing testosterone. Tadalafil can also enhance the testosterone-to-estrogen ratio by inhibiting the aromatase enzyme, and it increases androgen receptor density while improving lean body mass. It has been shown in human studies that you can expect to gain a couple pounds of lean mass and lose a couple pounds of fat from long-term Tadalafil use. Tadalafil improves bone strength and wound healing. It increases androgen receptors and decreases aromatase in osteoblast cell lines and was able to enhance fracture healing in a rat femur and improve bone density. Tadalafil also improves burn wound healing. Moving up to the brain, in elderly patients with erectile dysfunction, Tadalafil improves cerebral blood flow in the postcentral gyrus, precuneus, and brainstem, and enhances cognitive function, as assessed by the Montreal Cognitive Assessment Score. While it's uncertain if this effect occurs in younger men, Tadalafil has enhanced working memory in both young and old mice. Now let's get into how you should dose Tadalafil for maximum benefits and low side effects, even though its safety is well established. If you dose it too high, you may get occasional headaches, flushing, a stuffy nose, but there are two even worse side effects than that. One, muscle pain. Two, aortic damage and testicular toxicity. The muscle pain can occur because Tadalafil is a slight off target for PDE11 inhibition, which is known to cause muscle pain, especially back pain. At 5mg, this effect of Tadalafil is barely relevant, but it becomes more relevant once you go up to 10mg+. The aortic damage can occur due to oxidative stress combined with too much dilation. You see, Tadalafil is a hormetic stressor, as mentioned earlier, and this is how it increases endogenous antioxidant production, and is consistently shown to be net protective at 5mg human dosages. It's protective to the testes at these doses, as well, in both humans and mice who received an equivalent dose converted for their species. However, if you look at rodent studies, you will see that at a 20mg equivalent dose, that changes, and starts to have a net toxic effect. MDA levels increase, which are markers of oxidative stress, and antioxidant levels drop. The same case would be true if you did HBOT for 15 hours a week, which is hyperbaric oxygen chamber therapy. Some is great, but once you cross a certain threshold, it becomes toxic. This also relates to how some people using Tadalafil mention a slight dip in sex drive over time. This can occur if they are taking too high of a dose, usually 10mg+, and it can happen for a couple reasons. The first, is that it can start to induce oxidative stress in some people, as mentioned. And the second, is that it can reduce estrogen levels with long-term use, and estrogen is important for libido. This is why you need to use no more than 5mg a day, and also monitor your blood work for your testosterone to estrogen ratio. But you need to request LC-MS, MS, because this is the only accurate way to measure hormone levels. Doctors are mostly just concerned if something is within range, not if it's optimal. If your estradiol levels are near the low end of the range, and your testosterone levels are mid-range or high range, then you may consider adding in something to raise your estradiol up. DHEA or Omnibol, which contains pregnenolone and DHEA, is great for this, and Boron can help some people to a lesser extent, and also raise free testosterone slightly. In conclusion, Tadalafil is a fascinating and underappreciated compound with uses in healing broken bones, chronic wounds, heart damage, and increasing testosterone levels. For the best results, for both blood flow and stem cells, consider combining it with Vesugen, a tripeptide with a sequence lys-glu asked. To learn more, get the peptide mastery free edition on my website, linked in the description. You can also get our free guide, Toxic Testosterone, which reveals the hidden dangers of the 5 most commonly recommended testosterone supplements, and what to do instead. This has been Brenden Henry, the world's leading expert in peptide science.

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