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11th September 18:58
External User
Posts: 1
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Hi,
A few weeks back i approached Dr Bill Sardi about copying his vitamin C story in his Newsletter for a p post. We got to talking about psoriasis and he reported that he had a few folks who improved (their psoriasis) due to taking a supplement that he works with designed for moisturizing the skin. One thing lead to the next and I've taken six caps of HA twice a day for 13 days. HA is working beyond any expectations i had. After the first week i added in NAC twice a day and it boosted the HA a little more. My regular P diet plan is more or less in place. I have a ton of tests to run with HA. For all i know it could reverse tomorrow. Right now i'm living large and clear-ish and loving it. I'm gonna stick out my long neck and speculate that this is gonna be big. Longnecker big? Only if you want to pay me. Why shouldn't i get rich off you while clearing me? lol Here's what i'm taking, 3 caps of Purity's Vital H.A. Max formula twice a day. And 3 caps of Purity's Ultimate H.A. Forumula twice a day. I eat two meals a day and thats when i've taken (each six caps) so far. Here are some links, http://www.purityproducts.com/product.asp?sku=134 http://www.purityproducts.com/read_m...ultimateHA.htm I haven't tried this yet, but it may augment taking it orally, http://www.purityproducts.com/product.asp?sku=252 Here are a few abstracts, This one looks key, http://www.ncbi.nlm.nih.gov/entrez/q..._uids=15149843 Hyaluronan suppresses epidermal differentiation in organotypic cultures of rat keratinocytes. Hyaluronan (hyaluronic acid, HA) is an abundant matrix component between keratinocytes of the epidermis in vivo, but its function there remains unclear. We used a lift culture model, in which rat epidermal keratinocytes (REKs) stratify at an air-liquid interface, to ask whether HA may regulate epidermal proliferation and/or differentiation. In this model, early markers of differentiation (keratin 10), and later markers (profilaggrin, keratohyalin granules, cornified layers) are faithfully expressed, both temporally and spatially. HA, measured using two different analytical techniques, accumulated to high levels only in the presence of an intact basement membrane that seals the epidermal compartment. To test whether HA has a functional role in differentiation, Streptomyces hyaluronidase (StrepH, 1 U/ml; digests >95% of HA within 4 h) was added daily to lift cultures during stratification time-course experiments over 5 days. In StrepH-treated cultures, the expression of profilaggrin and the number and size of keratohyalin granules were significantly increased relative to controls using semiquantitative histological analyses. The StrepH-related accumulation of K10 protein and profilaggrin/filaggrin were confirmed by Western analyses. Thus, it appears that the presence of intercellular HA in the epidermis acts as a brake upon intracellular events that occur during keratinocyte differentiation. PMID: 15149843 Strep is one of the triggers of psoriasis. And anything that slows down differentiation is good for psoriasis. This next has a good idea for psoriasis also, upregulation of a key gene (HAS2) http://www.ncbi.nlm.nih.gov/entrez/q..._uids=15020224 Compound K induces expression of hyaluronan synthase 2 gene in transformed human keratinocytes and increases hyaluronan in hairless mouse skin. Ginsenosides, the major active ingredients of ginseng, have a variety of biomedical efficacies such as anti-aging, anti-oxidation, and anti-inflammatory activities. To understand the effects of compound K (20-O-beta-D-glucopyranosyl-20(S)-protopanaxadiol), one of the major metabolites of ginsenosides, on the skin, we assessed the expression levels of about 100 transcripts in compound K-treated HaCaT cells using cDNA microarray analysis. One gene up-regulated by compound K was hyaluronan synthase2 (HAS2). Semi-quantitative RT-PCR showed that compound K increased HAS2 mRNA in time- and dose-dependent manners. ELISA and immunocytochemistry using hyaluronan (HA)-binding protein showed that compound K effectively increased HA production in HaCaT cells. Finally, treatment of compound K on hairless mouse skin increased the amount of HA in the epidermis and papillary dermis. Our study suggests that topical application of compound K might prevent or improve the deteriorations, such as xerosis and wrinkles, partly ascribed to the age-dependent decrease of the HA content in human skin. PMID: 15020224 Looking at the surrounding genes may hold some clues. OMIN search of (HAS2) hits, 1: *601636 HYALURONAN SYNTHASE 2; HAS2 Gene map locus 8q24.12 Map: http://www.ncbi.nlm.nih.gov/entrez/q...st_uids=601636 2: *602428 HYALURONAN SYNTHASE 3; HAS3 Gene map locus 16q22.1 map: http://www.ncbi.nlm.nih.gov/entrez/q...st_uids=602428 What do we have in the group for it? (J's mentioned it! So has evetsm!) http://groups.google.com/groups?hl=e...ases.psoriasis Hyaluronic acid --diet anyone? http://groups.google.com/groups?q=Hy...eja.com&rnum=2 How to get Hyaluronic acid in your diet: Hyaluronic Acid supplements are now available in easy to consume capsules. http://www.hyaluronic-acid.org/ Web search of HA, http://www.miragemedical.co.uk/restylane.htm Gif: http://www.medscape.com/pi/editorial...ll/slide06.gif Taken from: http://www.medscape.com/viewprogram/264_pnt Have a Happy HA day. |
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11th September 18:58
External User
Posts: 1
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So I can maybe throw in some alpha-lipoic acid I have sitting around.
The logic is sweet, and if I get major clearing from it I'll want to buy the world a Coke, and maybe a bit more for you personally! Maybe we can get TJ's to start carrying it. I do like the sound of it, BUT wonder how much of it gets through the stomach undigested. Well, maybe if digestion breaks it apart, the body puts it right back together, and closer to where it's needed!??!?! Blended with this and that, no pure source? Well, screw that if it's working, but maybe go back later and figure it out. Wondered about it topically, but it's a big, fat polymer so it's not going to be absorbed. Moi? As an ingredient for a topical someone else mentioned, and I didn't even pick it out as the significant ingredient. Chemicals got their own web sites? Oh, brave new world! Well, I think I'll give the turmeric another week or three, but you've definitely got me to put HA on the top of the list of things to try next! And, meanwhile, eat less meat, maybe a bit more magnesium, less iron, fewer total calories. A high carb diet, boy, you *really* gotta reduce the total calories! (and in fact, I have to wonder if that's not the real reason those Japanese villagers lived longer, it's pretty clear now that that works, but I guess the HA helps with quality of life, maybe, hopefully). See if my local Japanese joint has a vegetarian bento lunch ... http://www.kabukirestaurants.com/pub...91528338117861 Well, salmon teriyaki, with that farmed salmon (ugh), plus or minus the tempura, good, but tempura includes an evil iron-containing shrimp, not to mention evil trans-fatty acids in the fry oil. Hmm, maybe I can negotiate a pure veggie tempura deal, triple sweet-potato, yum, and maybe they can throw in some onions and broccoli, which they don't now tho other places do. Local chain, doesn't even reach to San Diego, I do recommend the bento lunches and boat dinners and such, but do NOT go there for sushi!!! J. |
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11th September 18:58
External User
Posts: 1
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If you have ROS why not? Ala + ALC would be optimal. You may make
it to 100 without the HA skin fix treatment. Sweet! Its the real thing. I'll be eating it raw from some cocks comb before long. ![]() You got me. At the time i figured it couldn't hurt. They use young chicken breast bones. Besides the cocks combs and some microbial preparation, its the most plentifull source. Ok, lets try a few more abstracts. Still worth a try. If it pulls in moisture to the skins top surface and has HA trying to get in from the inside, maybe some sort of synergy will develop. And since my skin is looking so nice, it may make it look even better. ![]() I did use the wheatgrass yesterday and its looking fine. Recognize that elevated HA levels in blood serum indicates more HA is being degraded. For those who wish to learn more, HOW TO LIVER 100 YEARS WITHOUT GROWING OLD (www.hereandnowbooks.com). Clin Rheumatol. 2000;19(6):455-7. . Serum levels of hyaluronic acid in patients with psoriatic arthritis. Elkayam O, Yaron I, Shirazi I, Yaron M, Caspi D. Department of Rheumatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. oribe14@netvision.net.il The purpose of this study was to evaluate the serum levels of hyaluronic acid (HA) in a group of patients with psoriatic arthritis (PsA), with special emphasis on the relationships between HA levels and clinical parameters of joint and skin activity. Thirty-four patients with PsA, 34 patients with rheumatoid arthritis (RA) and 49 healthy volunteers participated in the study. Assessment of joint disease in patients with PsA included duration of morning stiffness, number of tender and swollen joints, right and left grip, the presence of inflammatory back pain and Schober's test. The current severity of skin involvement was graded according to the Psoriasis Area Severity Index (PASI). Serum levels of HA were measured by a radiometric assay. The mean HA serum levels of patients with PsA and RA were significantly increased in comparison with healthy controls (107 +/- 39.6 microg/dl in patients with PsA, whereas in patients with RA it was 168 +/- 32.4 microg/dl and 36.7 +/- 5.5 microg/dl in healthy controls). A highly significant correlation was found between levels of HA and index of skin involvement, but no association was found between HA levels and clinical parameters of joint severity. We conclude that in this cohort of patients with PsA, HA levels clearly reflected psoriatic skin involvement although it did not correlate with joint disease. Arch Dermatol Res. 1994;286(1):21-9. . Hyaluronan and CD44 in psoriatic skin. Intense staining for hyaluronan on dermal capillary loops and reduced expression of CD44 and hyaluronan in keratinocyte-leukocyte interfaces. Tammi R, Paukkonen K, Wang C, Horsmanheimo M, Tammi M. Department of Anatomy, University of Kuopio, Finland. The distributions of hyaluronan (HA) and its presumptive receptor, CD44, were studied in skin samples from 13 psoriasis vulgaris patients, using an HA-specific probe (HABC), and monoclonal antibodies, respectively. The general distribution of HA and CD44 in psoriatic lesional epidermis resembled that in normal epidermis. However, areas of epidermis invaded by leukocytes showed a local depletion of HA and CD44, particularly at the contact areas of keratinocytes to lymphocytes and neutrophils. Removal by cellular uptake or extracellular degradation of CD44 and HA may be required for tight adherence between a keratinocyte and a leukocyte. On the dermal side, the tips of the prolonged dermal papillae in psoriatic lesions were intensively stained with HABC. The dilated capillaries and the space below the tip basal lamina, in particular, were heavily covered with HA. Occasionally, a similar intense staining was seen around an enlarged capillary in uninvolved psoriatic skin. CD44-positive leukocytes were found around the affected capillaries. The accumulation of HA in the dermal papillae may support the growth of psoriatic lesions, since HA stimulates the growth of capillaries as well as attracting inflammatory cells. Br J Dermatol. 1985 Jun;112(6):663-71. . Circulating hyaluronate in psoriasis. Lundin A, Engstrom-Laurent A, Hallgren R, Michaelsson G. A radioassay method allowing measurements of low concentrations of circulating hyaluronate was used in a study of serum hyaluronate concentrations in 44 patients with psoriasis. Twenty-three of them had only skin lesions and 21 had both skin lesions and arthropathy. In both of these groups significantly elevated serum levels of hyaluronate were found. The highest values were observed in those with widespread and active skin disease and/or active arthritis. Serum hyaluronate positively correlated with the plasma concentrations of alpha 1-antitrypsin and haptoglobin and also with ESR, which may indicate a relationship between acute inflammation and increased production of hyaluronate. Seven patients with widespread atopic dermatitis included for comparison had normal hyaluronate values. In blister fluid from lesional skin in two patients with acute psoriasis, very high concentrations of hyaluronate were found, in comparison with the concentrations in blister fluid from non-involved skin. The increased concentration of serum hyaluronate in psoriasis indicates involvement of dermal and synovial tissue in psoriasis, in addition to the epidermal changes &&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&& Somethings amiss here. HA is high in the skin of psoriatics and i'm taking HA and my P is going bye bye. Rather counter-intuitive at this point. Degraded HA in the skin seems to be a problem for psoriatics. I wonder whats happening with the HA supplements as far as clearing my P? Oh and one more thing. In my haste i posted that Bill Sardi was Dr Bill Sardi. My mistake. Bills a health journalist. His articles are so insightfull, its hard not to think of him as anything other then a healer. And better yet, many of his articles aim for the prevention of disease and that makes as much sense as living to 100 and not enjoying the triP. Ha-PP-y P trails |
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