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i think after xifaxan i dont absorb RS.maybe xifaxan killed bacteria needed for RS degrading.i ordered primal defense,prescript assist,bacillus coagulans and aor 3 .are these probiotic supplements will help with this?
Generally speaking, mice, rats and pigs make excellent laboratory proxies for humans.
I'm afraid not. Animal models are no better at predicting outcomes in humans than tossing dice. If you don't believe me, have a look at some quotes (mostly from scientists) in my blogpost here.
i think after xifaxan i dont absorb RS.maybe xifaxan killed bacteria needed for RS degrading.i ordered primal defense,prescript assist,bacillus coagulans and aor 3 .are these probiotic supplements will help with this?
ok thanks.you use any probiotics?Hi finalgates,
I am not sure I understand your post (because I am in no way a scientist! ) but, just to comment, I have taken several courses of xifaxin over the years (it killed off a massive prevotella overgrowth) yet I am getting some significant responses to RS.
I have been a bit superstitious about reporting good results since we all know that it is hard to pin down "what is affecting what" but so far so good.
Best,
Sushi
ok thanks.you use any probiotics?
The effect of lactulose, pectin, arabinogalactan and cellulose on the production of organic acids and metabolism of ammonia by intestinal bacteria in a faecal incubation system
An in vitro faecal incubation system was used to study the metabolism of complex carbohydrates by intestinal bacteria. Homogenates of human faeces were incubated anaerobically with added lactulose, pectin, the hemicellulose arabinogalactan, and cellulose, both before and after subjects had been pre-fed each carbohydrate. Fermentation of added substrate was assessed by the production of short-chain fatty acids (SCFA) and suppression of net ammonia generation over 48 h of incubation. Control faecal homogenates to which carbohydrate was not added yielded an average increment of SCFA of 43 mmol/l, equivalent to 172 mmol/kg in the original stool. The addition of lactulose, pectin and arabinogalactan each increased the yield of SCFA by a similar amount, averaging 6·5 mmol/g carbohydrate or 1·05 mol/mol hexose equivalent; organic acid yield was not increased by pre-feeding these substances for up to 2 weeks. Acetate was the major SCFA in all samples at all times and, after pre-feeding with extra carbohydrate, butyrate concentrations exceeded propionate in all samples. Faecal homogenates incubated with cellulose showed no greater SCFA production than controls over the first 48 h, but there was a slight increase when samples from two subjects pre-fed cellulose were incubated for 14 d. Net ammonia generation was markedly suppressed by addition of lactulose to faecal incubates with an initial period of net bacterial uptake of ammonia. Pectin and arabinogalactan also decreased ammonia generation, but the reductions were not significant unless subjects were pre-fed these materials; cellulose had no effect on ammonia generation.[LINK]
Larch arabinogalactan: clinical relevance of a novel immune-enhancing polysaccharide.
Larch arabinogalactan is composed of greater than 98-percent arabinogalactan, a highly branched polysaccharide consisting of a galactan backbone with side-chains of galactose and arabinose sugars. Larch arabinogalactan is an excellent source of dietary fiber, and has been approved as such by the FDA. It has been shown to increase the production of short-chain fatty acids, principally butyrate and propionate, and has been shown to decrease the generation and absorption of ammonia. Evidence also indicates human consumption of larch arabinogalactan has a significant effect on enhancing beneficial gut microflora, specifically increasing anaerobes such as Bifidobacteria and Lactobacillus. Larch arabinogalactan has several interesting properties which appear to make it an ideal adjunctive supplement to consider in cancer protocols. Experimental studies have indicated larch arabinogalactan can stimulate natural killer (NK) cell cytotoxicity, enhance other functional aspects of the immune system, and inhibit the metastasis of tumor cells to the liver. The immune-enhancing properties also suggest an array of clinical uses, both in preventive medicine, due to its ability to build a more responsive immune system, and in clinical medicine, as a therapeutic agent in conditions associated with lowered immune function, decreased NK activity, or chronic viral infection. [LINK]
As a biological response modifier, larch arabinogalactan also appears to offer substantial promise. The currently documented effects on NK (Natural Killer (immunology) cytotoxicity, along with its effects on the function of the mononuclear portion of the immune system, suggest an array of clinical uses both in preventive medicine, due to its ability to build a more responsive immune system, and in clinical medicine, as a therapeutic agent in conditions associated with lowered immune function or decreased NK activity.
The prophylactic applications might include use as an immune-building agent for individuals with a propensity to ear infections and other upper respiratory infections. As a therapeutic agent, LARCH ARABINOGALACTAN APPEARS TO HOLD THE MOST PROMISE AS AN AGENT IN CONDITIONS CHARACTERIZED BY REDUCED NK ACTIVITY AND CHRONIC VIRAL INFECTIONS, SUCH AS CFS and viral hepatitis.[LINK]
barley and ota grass what role have in prImal defense?they have SBO?
Interesting info on Lactulose and Arabinogalactan. Arabinogalactan is a prebiotic fiber usually sold as Larch Arabinogalactan (it comes from the bark of the larch tree). I see it's a major component of Prebiogen, which Chris Kresser sells. Seems to be expensive as hell, but it seems to be one of the fibers that can help modulate the gut flora to decrease ammonia, which I know is desirable with this crowd:
Therapy of chronic fatigue syndrome
Chronic fatigue syndrome (CFS) is characterized by unexplained, debilitating fatigue or easy fatigability lasting longer than six months. While a number of clinical trials have been performed in CFS patients, there is currently no established therapy for CFS. Treatment with acyclovir of CFS patients is ineffective. Intravenous immunoglobulin therapy appears to be effective, though the results are controversial. Antidepressants might help the associated depression and anxiety but not other symptoms. Trials with magnesium have improved the well-being of patients. Restoration of NK activity by biological response modifiers, such as sizofirann, resulted in restoration of NK cell activity and recovery from CFS. Taken together, immunological abnormalities may be involved in CFS, and its restoration may produce clinical benefit in CFS. [LINK]
Just got my thyroid test result:
TSH 0.72 (0.4 - 3.7)
T3 4.6 (3.6 - 6.3)
T4 20 (12 - 22)
So they all look normal. And older test a few years back, looked like this, definitely some changes:
TSH 1.3
T3 4.3
T4 13
Whether this is due to RS, iodine or a combination of factors, I can't say. I would be interested in seeing whether cortisol and aldosterone has gone up as well.
EDIT #3: I'm almost positive that Kresser's Prebiogen is actually re-branded Biotagen, which is much more affordable from Amazon (about half the price). Those products aren't a pure arabinogalactan, but a variety of fibers are often a desirable quality. For instance, it also has Beta-glucan, which has a number of immune-enhancing properties similar to arabinogalactan.
More details on Biotagen can be found here:
http://www.klaire.com/prod/proddetail.asp?id=K-BTG
I'm away from home at the moment and many, many miles from my RS stash but I thought I'd update anyway...
I haven't used any RS for 13 days now, (or any probiotics for more than a week) and I'm continuing to have the lower body lymph swelling/burning. I ran a temperature on and off for the best part of 3 weeks, and had a very sore throat on and off but that's stopped now. It's early autumn here and everyone around me is well. Apart from the lymph I'm now feeling very well, and I wish I could back to the RS but feel I should maybe hold off a bit longer.
FWIW, last week a nurse friend suggested my symptoms were similar to what she'd seen with systemic toxo gondii infection. I have congenital toxoplasmosis (a flare up of which at adolescence kicked off my ME) but I have had no symptoms of an infection (and titre has remained stable) since 1999. I don't know if protozoal infection is playing any part in my response to RS or not, but so far I don't seem to be having the more typical reaction of gas/sulfur ==> gradual improved tolerance..
@Vegas you mentioned the lymph symptoms, and protozoa back there too....I'm curious as to whether you've had toxo gondii exposure in the past? Anne.
Ha, that's truePretty crazy. Looks like @adreno noticed this a few years ago.
Well actually lower TSH would indicate more thyroid activity. In any case I feel overstimulated, not under.@adreno, something I learnt About thyroid (My CFS Dr told me) is if I have it closer to TSH 0.5 than to 1.0 My signaling slows down. Is not exactley Brain fog but example: You ask me 2+2 and then I have to think about what you just told me (Translating the questions in to what you just said, not the actual calcualtion, I haven't even make it that far....that kind of signaling) will be too slow. So like you are under TSH 1.0 watch for that. Just a thoguht.
...
As to you present condition, I would operate under the assumption that the your symptoms are a clear manifestation of your improved ability to generate an immune response. This is not complicated, it is just a foreign experience to many, and the cumulative effects of sustained "immunoincompetence" have to be taken into consideration. There will be adverse consequences, even when there is no apparent stimulus, as you have experienced two weeks after the RS.
The lymph node you describe in the arm, assuming the right arm, is part of a different lymphatic channel altogether separate from the messenteric lymph nodes. If you are referring to the right arm, this may suggests that you have more than just the GIT infection, although not necessarily. As to whether this is a consequence of toxoplasmosis, I don't know.
My experiences have been very similar. I waited 10 days after the last tsp. The lymphatic pain by that time had largely but not totally subsided, and I was feeling pretty well. Then I took another tsp yesterday, and today I am having what I would describe as a true Herx reaction. chills, nausea, headache, body ache, ice cold hands, fatigue. I'm so over the RS experiment.
Seriously, I am seeing some good things, but 1 tsp is absolutely killing me, again.
In retrospect I am beginning to wonder if the initial success of the 2 week golden period of when I first tried Candex (never to be replicated again) was due to a massive pre-biotic effect. Supposedly up to 60% of the cell wall of Candida can be made of beta-glucan. I think that perhaps when I first tried Candex enzymes it tore up a massive amount of Candida and liberated beta-glucans on a large scale which then had a huge prebiotic effect and a positive immune stimulating effect. Not only was I destroying something bad I was perhaps more importantly feeding the good guys in one fell swoop. I think you had theorized something like this as well Ripley IIRC.