On 24/11/2015 8:37:35, trantran83333 said:
You are from Adelaide, right?
On 11/23/2015, 2:52:57, trantran83333 said:*blood results*
A few of your liver enzymes got worse since 2012.That's something to note. Did you change your diet or lifestyle for the worse since 2012 or do you believe it to be strictly caused by the accutane? Your liver enzymes do not need to be higher than the reference range to indicate a problem by the way. Most path labs just use the local population's results averaged together. (The normal people getting their blood taken (mostly unhealthy people).
One example is AST and ALT. The ref range usually goes from like 5 up to40 or 50 IU/L but I've seen doctors who say there is pathologywhen the enzymes are as low as23-25.
One thing to note is that AST isn't specific to the liver as ALT is. High AST could indicate cell death in other parts of your body.
Your LD seemselevated as well. Yours: 143-175 U/L
According to some sources, the normal Adult Range: 45 - 90 U/L
Again, reference ranges vary wildly among labs. Some may suggest higher is normal.
Pay attention to patterns as well. Yours seems to have gotten worse.
LDH (Lactic Acid Dehydrogenase)is an enzyme found in many body tissues, including the liver. Elevated levels of LDH may indicate liver damage. Increases are usually found in cellular death and/or leakage from the cell or in some cases it can be useful in confirming myocardial or pulmonary infarction (only in relation to other tests). Decreased levels of the enzyme may be seen in cases of malnutrition, hypoglycemia, adrenal exhaustion or low tissue or organ activity"
Remember, high levels of retinoic acid in the liver can cause extreme oxidation of the tissues and cell death as shown in the vitamin A toxicity youtube video I posted a while back.
When is your next liver & gallbladder flush? I'm actually experiencing increased energy and better digestion since my last flush a couple weeks ago. I should also mention that I startedtaking taurine 1-2g/day a few days ago as well.
Has anyone seriously thought about getting a lawyer?
I got some chart notes from my ole derm. They finally arrived. So i cracked the thick style yellow envelope open and looked at all of the information the doctor wrote before, as, and after "treatment"
Here are a few snaps i took. Not to hold onto the depression, but if these interest anyone please give them a read. I have been experiencing all of the mental sode effects listed in this warning pamplet from 2009.
[Edited image out]
On 11/27/2015 6:09:07, trantran83333 said:How are you these days oli girl?
On 11/27/2015 6:09:07, trantran83333 said:How are you these days oli girl?
I am doing okay! I still have my days, but things have been better once I got a official dx! I took a year off from the forum and others to have a break which is sometimes a good thing. I try to live life to the fullest everyday as I don't know when it might not be here... My dream has always been to travel the world, so my daughter is graduating this year and when she goes off to college that exactly what I am going to do
I hope your doing well!
I really love hearing stuff that says - Roaccutane induced and the word "irreversible".......that just gives me so much faith yeah.....
Surely theseare grounds for us all to sue these mongrels for leading us to this position in life!!?
I have swollen legs and major varicose vein issues- not sure this whole taurine supplementing thing that everyone is tryingis the answer to ourproblems?
I'm really considering doing those water fasting detoxes..... Thats the last thing I can think to do till some Scientist/Doctor works out what the fuck we should do to fix this situation!?
Thanks for all the info to those doing great research - much appreciated!!
On 24 November 2015 8:07:35 pm, trantran83333 said:
From Wikipedia
https://en.wikipedia.org/wiki/Alanine_transaminase
"Significantly elevated levels of ALT (SGPT) often suggest the existence of other medical problems such as viral hepatitis, diabetes, congestive heart failure, liver damage, bile duct problems, infectious mononucleosis, or myopathy, so ALT is commonly used as a way of screening for liver problems. Elevated ALT may also be caused by dietary choline deficiency. However, elevated levels of ALT do not automatically mean that medical problems exist. Fluctuation of ALT levels is normal over the course of the day, and they can also increase in response to strenuous physical exercise."
https://en.wikipedia.org/wiki/Taurine#Physiological_functions
"Taurine has also been shown to help people with congestive heart failure by increasing the force and effectiveness of heart-muscle contractions"
This is backed up by tonnes of studies btw. The only reason I checked this out was because I notices ALT and AST were the markers that changes most drastically with accutane, and I'd already looked up taurine so when I read congestive heart failure I instantly linked it, whether correctly or incorrectly... Anyway, could mean nothing, just food for though. Thanks for the before and after TT83!
On another note why are so many sufferers Australian? I wonder if there are any differences between Roaccutane and Accutane, or if the prescribed amount differed?
Over the years I've received emailsfrom many all over the worldwith side effects (even one in Pakistan) However,I think you'll see more US, UK, AUS, & CAN victimsbecause ofthe western markets being saturated withdrugs in general. It probably comes down to politics and just a more readily available free market for business (even at the expense of personal health). I know I've read that the Japanese ministry of health actually banned Accutane from being sold in their country after several casesof adverse effects and studying the drug themselves. It would be interesting if we had some genetic predisposition to Retinoid toxicity seeing as how some of us don't come from cold snowy climates (Switzerland) And we know the most amounts of Vit A are in the livers of Huskies, Polar bears, Cold water fish/whale. It is some evolutionary adaptation to survive in cold environments. Although this probably isn't the case as I'm sure there are adverse cases in the Swiss population themselves.
1 hour ago, Fchawk said:
From Wikipedia
https://en.wikipedia.org/wiki/Alanine_transaminase
"Significantly elevated levels of ALT (SGPT) often suggest the existence of other medical problems such as viralhepatitis,diabetes,congestive heart failure, liver damage,bile ductproblems,infectious mononucleosis, ormyopathy, so ALT is commonly used as a way of screening for liver problems. Elevated ALT may also be caused by dietarycholinedeficiency. However, elevated levels of ALT do not automatically mean that medical problems exist. Fluctuation of ALT levels is normal over the course of the day, and they can also increase in response to strenuous physical exercise."
https://en.wikipedia.org/wiki/Taurine#Physiological_functions
"Taurine has also been shown to help people withcongestive heart failureby increasing the force and effectiveness of heart-muscle contractions"
This is backed up by tonnes of studies btw. The only reason I checked this out was because I notices ALT and AST were the markers that changes most drastically with accutane, and I'd already looked up taurineso when I read congestive heart failure I instantly linked it, whether correctly or incorrectly... Anyway, could mean nothing, just food for though. Thanks for the before and after TT83!
On another note why are so many sufferers Australian? I wonder if there are any differences between Roaccutane and Accutane, or if the prescribed amount differed?
It the same I was on 20mg a day.
it's relatively easy and cheap to get here packet of 60 is only $13 if I remember correctly. The government pays for the rest. I don't know how much they cost in America
1 hour ago, macleod said:Over the years I've received emailsfrom many all over the worldwith side effects (even one in Pakistan) However,I think you'll see more US, UK, AUS, & CAN victimsbecause ofthe western markets being saturated withdrugs in general. It probably comes down to politics and just a more readily available free market for business (even at the expense of personal health). I know I've read that the Japanese ministry of health actually banned Accutane from being sold in their country after several casesof adverse effects and studying the drug themselves. It would be interesting if we had some genetic predisposition to Retinoid toxicity seeing as how some of us don't come from cold snowy climates (Switzerland) And we know the most amounts of Vit A are in the livers of Huskies, Polar bears, Cold water fish/whale. It is some evolutionary adaptation to survive in cold environments. Although this probably isn't the case as I'm sure there are adverse cases in the Swiss population themselves.
We need a great doctor to talk with him , we need a doctor who knows the bloody side of the accutane. But i never saw anyone. Anyways there is a university who makes search on post finasteride victims. If the study have done with succsess , they would find the real problem about us ! Accutane and Finasteride is in the same league. So i still have hope. Let's see what we can get !
On 11/24/2015 at 5:37 PM, trantran83333 said:
Just been reading some studies and looking at various websites regarding liver damage, and Ive noticed that your liver tests would potentially indicate fatty liver, which TTH2014 has already suggested could be a/the consequence of accutane for the people who suffer from persistent side effects. Youve got evaluated ALT and slightly elevated AST
- Typically elevations in liver enzymes whereby the level of ALT elevation is higher than the level of AST elevation could be an indicator of fatty liver or NASH (Nonalcoholic Steatohepatitis)
- Therefore, one can presume a diagnosis of fatty liver or NASH based on signs of insulin resistance, elevated ALT levels for a long duration, signs of fatty liver through imaging and exclusion of other causes of elevated ALT levels and fatty liver
Source: [Edited link out]
Fatty liver is also indicated by a mild pain of discomfort in the liver area (under your right rib). Ive suffered from this since taking tane, and have had ultrasound scans on the area, and a various blood tests done (but not a full liver panel).
Fatty liver itself isnt a massive issue, but it develops into Cirrhosis which can be. Causes of Cirrhosis include¦
- Excessive intake of vitamins such as vitamin A. Being fat-soluble, vitamin A is stored to a variable degree in the body (liver), making it more likely to cause toxicity when taken in excess amounts
Fatty liver develops as follows;
Fatty Liver -> NASH (Nonalcoholic Steatohepatitis) -> Cirrhosis
Would be interesting to know if anyone suffering from accutane side effects has had a liver transplant. My guess would be this cured them of their side effects. Obviously this is not really a realistic solution, but the root cause of the sides is almost certainly liver damage.
Some interesting reading on [Edited link out] though for anyone whos interested
Treatments for Fatty live, NASH, Cirrhosis?
Interestingly one suggested treatment for Cirrhosis is SAMe, which was used in a study a while back that showed mitigation of isotretinoin side effects when supplemented along with the drug in this study;
http://lib.dr.iastate.edu/etd/13056
Study on the importance of SAMe (I know this has already been mentioned a number of times on this thread)
- S-Adenosyl-L-methionine (SAMe) exerts many key functions in the liver, including serving as a precursor for cysteine, 1 of 3 amino acids of glutathione--the major physiologic defense mechanism against oxidative stress
- The precursor of SAMe is methionine, one of the essential amino acids, which is activated by SAMe-synthetase (EC 2.5.1.6). Unfortunately, the activity of this enzyme is significantly decreased as a consequence of liver disease.
Something which Ive noticed in this study which is interesting is that methionine is apparently increased, and thus reduces SAMe. Ive been eating lots of brazil nuts to supplement methionine, but this I might hold off now..
- Because of decreased utilization, methionine accumulates and, simultaneously, there is a decrease in SAMe that acquires the status of an essential nutrient and therefore must be provided exogenously as a supernutrient to compensate for its deficiency
http://www.ncbi.nlm.nih.gov/pubmed/12418503
Sounds like additional methionine should actually be avoided, and maybe SAMe takeninstead?
I've just ordered NAC which apparently increases production ofGlutathione, and sounds like taking that along with SAMe could be beneficial based on the above study. Continuing with taurine too for the foreseeable.
5 hours ago, Mike San said:They aren't elevated though.
Yeah I misinterpreted the results! They actually look quite in range looking again. There is at least one study showing that isotretinoin raises AST and AST levels, however looking at one of these studies, it's not by a massive amount (but possibly enough to throw things out of balance). Would be very interesting if there was a follow up study to find out if any of the participants developed side effects from the drug, and whether they were the ones with elevated levels;
http://www.ncbi.nlm.nih.gov/pubmed/22714752
- Of the 130 patients who received isotretinoin between January and December 2009, only 70 were actually treated for 3 months or more and handed in the results of their laboratory tests. Of these 70 patients, 39 (55.7%) were female. The mean age of the women (23.9 years) was higher than the mean age of the men (20.1 years). There was a statistically significant increase in the levels of triglycerides (87.01 48.25 versus 105.32 48.76 mg/dL), AST (20.44 6.26 versus 24.38 11.92 U/L) and ALT (18.24 8.31 versus 23.34 20.03 U/L) performed prior to and 3 months or more after oral isotretinoin treatment. After treatment with oral isotretinoin, triglyceride levels had increased beyond the normal range in 11% of the patients, while 8.6% had elevated AST levels and 7.3% had increased ALT levels.
4 hours ago, Modeaa said:
"(Ro)accutane induced irreversible proteinuria
...(Ro)accutane is found to cause a statistically significant induction of TGF-beta1 in several independent studies. Six weeks of isotretinoin treatment caused a statistically significant 19% increase in suction blister fluid TGF-beta1 [1]. There are no measured values of the cumulative effect after 3-4 months exposure, which is common in acne-subjects. Various studies have shown that significantly increased TGF-beta1 correlate with with the amount of urinary protein excretion (proteinuria and albumineria),in adose, but also importantlytimedependent manner. This due to failure in the kidney, of renal proximal tubular protein reabsorbtion. This is of major importance, because a significant failure in reabsorbtion leads to the loss of important vitamins, hormones and amino-acids [2]."
https://www.raypeatforum.com/forum/viewtopic.php?t=5119
"Taurine is a naturally occurring beta-amino acid produced by methionine and cysteine metabolism. It is involved in a variety of physiological functions, including immunomodulatory and antifibrotic. Taking advantage of the ability of human hair follicle grown in vitro to recapitulate most of the characteristic features of normal hair follicle in vivo, we studied (i) taurine uptake by isolated human hair follicles; (ii) its effects on hair growth and survival rate; and (iii) its protective potential against transforming growth factor (TGF)-beta1, an inhibitor of in vitro hair growth and a master switch of fibrotic program. We showed that taurine was taken up by the connective tissue sheath, proximal outer root sheath and hair bulb, promoted hair survival in vitro and prevented TGF-beta1-induced deleterious effects on hair follicle."
http://www.ncbi.nlm.nih.gov/pubmed/18489269
The restorative effect of taurine on experimental nonalcoholic steatohepatitis.
Abstract
Our objective was to explore the restorative effect of taurine on experimental nonalcoholic steatohepatitis (NASH). Thirty-six SD rats were randomly divided into three groups, 12 in each group: the normal group was fed standard rat diet; the model group and the treatment group were both fed a high-fat rat diet for 12 weeks, and the rats in the treatment group were simultaneously injected with taurine subcutaneously for 8 weeks. Hepatic histological change was observed; TNF-alpha and TGF-beta(1) protein expression was identified by immunohistochemistry; mRNA expression of TNF-alpha, TGF-beta(1), type I procollagen, and adiponectin was measured by RT-PCR; body weight, weight gain, liver weight, and liver index were measured; and biochemical parameters monitored included serum transaminases, serum lipids, fasting plasma glucose, and hepatic level of oxidative stress. Rats in the model group showed a significant increase in liver weight, liver index, serum transaminase activities, serum triglyceride, fasting plasma glucose, and oxidative stress; the mRNA expression of TNF-alpha, TGF-beta(1), and type I procollagen increased, whereas the expression of adiponectin decreased significantly, compared with that in the normal group. The typical hepatic lesions of NASH were observed histologically in the model group. Taurine treatment resulted in a significant decrease in liver weight, liver index, serum transaminase activities, serum triglyceride, fasting plasma glucose, and oxidative stress; the mRNA expression of TNF-alpha, TGF-beta(1), and type I procollagen decreased, but the expression of adiponectin increased significantly, compared with that in the model group. Histological improvement was observed in the treatment group. In conclusion, taurine could inhibit lipid peroxidation, improve lipid and glucose metabolism, decrease synthesis of TNF-alpha and TGF-beta(1), promote synthesis of adiponectin, and have a restorative effect on experimental NASH.
If im reading this right, not only does accutane deplete taurine, it also downregulates the enzyme that is needed to produce it naturally from methionine and cysteine by inducing the TGF beta 1
Branched-chain amino acids inhibit the TGF-beta-induced down-regulation of taurine biosynthetic enzyme cysteine dioxygenase in HepG2 cells.
http://www.ncbi.nlm.nih.gov/pubmed/24553827
Taurine deficiency has been suggested to contribute to the pathogenesis and complications of advanced hepatic diseases. The molecular basis for a low level of taurine associated with hepatic failure is largely unknown. Using carbon tetrachloride (CCl4)-induced cirrhotic rat model, we found that the activity and expression of cysteine dioxygenase (CDO), a rate-limiting enzyme in taurine synthesis, were significantly decreased in the liver of these rats. To investigate the underlying mechanisms for the suppression, we examined the effects of pathological cytokines on CDO expression in human hepatoma HepG2 cells. Among the several cytokines, transforming growth factor- (TGF-), one of the key mediators of fibrogenesis, suppressed Cdo1 gene transcription through the MEK/ERK pathway. Finally, we further examined potential effects of branched-chain amino acids (BCAA) on CDO expression, as it has been reported that oral BCAA supplementation increased plasma taurine level in the patients with liver cirrhosis. BCAA, especially leucine, promoted Cdo1 gene transcription, and attenuated TGF--mediated suppression of Cdo1 gene expression. These results indicate that the low plasma level of taurine in advanced hepatic disease is due to decreased hepatic CDO expression, which can be partly attributed to suppressive effect of TGF- on Cdo1 gene transcription. Furthermore, our observation that BCAA promotes Cdo1 expression suggests that BCAA may be therapeutically useful to improve hepatic taurine metabolism and further suppress dysfunctions associated with low level of taurine in hepatic diseases.
4 hours ago, Modeaa said:4 hours ago, Modeaa said:
there where talking about a possible methionine deficiency due to hyper glycine n-methyl-transferase enzyme which accutane cause in the liver. the first link you puted mention it too.
the second link didn't seem to be in related to accutane, but in this problem that it describe as decreased methionine utilization i wonder if beside SAMe just andenosylcoblamin might work just as well or even better because it could balance the methionine to adenosyl ratio, in case that adenosyl deficency was the cause for the reduced SAMe and that the excess methionin might have consequences.
more cases for P5P and taurine supplementaion:
Effect of vitamin B6 deficiency on the synthesis and accumulation of S-adenosylhomocysteine and S-adenosylmethionine in rat tissues.
http://www.ncbi.nlm.nih.gov/pubmed/11575573
We infer that the alteration of B6 metabolism, especially the reduction of PLP contents in liver and thymus, caused by the B6 deficiency, resulted in accumulation of SAH as well as reduction of SAM and the SAM/SAH ratio. The reduction of the SAM/SAH ratio was due to a block in the catabolism of methionine via the trans-sulfuration pathway. These may lead to inhibition of transmethylation reaction of DNA, RNA and protein, the synthesis and function of thymic lymphocyte and result in damage to tissues.
http://www.ncbi.nlm.nih.gov/pubmed/18547794
Furthermore, the key cofactor of transsulfuration, pyridoxal-5'-phosphate, significantly declined in the plasma after a week of the ethanol intervention, whereas an increase was observed in brain tissue. Under taurine supplementation, some recoveries were shown by delaying taurine depletion to Week 2, increasing the SAM/SAH ratio and elevating plasma and brain levels of vitamin B6 in Week 2. In conclusion, daily consumption of 30% alcohol interfered with SCAA metabolism, thus decreasing taurine's role in neurotransmission. The possible mechanism involved might be that ethanol interrupts the production of cysteine, which is the upstream SCAA of taurine, thus decreasing the homocysteine level. Additionally, taurine supplementation delayed this process.
Hey guys, many of us with the erectile dysfunction Problem. What Do you guys think of increasing SRD5a1? The Gene/Enzyme for dht.. Some report good feelings after drinking alcohol. Now I have read, that it increases SRD5a1 wich is significantly reduced by accutane... Think about it and let me know I don't know if There are natural ways to Do this. On Amazon.com there is real human SRD5a1 but very extensive! It could be, that together we get back our good feelings. Maybe.. This Forum helps me a Bit in my Situation. Greetings
1 hour ago, AlanTookAccutaneWow said:I say go straight for the liquor
But trying SRD5a1 he won't be drunk.
1 hour ago, manalesenicola said:What Do you guys think of increasing SRD5a1? The Gene/Enzyme for dht..
Sounds interesting. We should find people who tried it and shared their effects after SRD5a1.
Has anyones oil returned after treatment? its been 5 years post accutane and my skin has been dry as a desert
7 hours ago, manalesenicola said:Hey guys, many of us with the erectile dysfunction Problem. What Do you guys think of increasing SRD5a1? The Gene/Enzyme for dht.. Some report good feelings after drinking alcohol. Now I have read, that it increases SRD5a1 wich is significantly reduced by accutane... Think about it and let me know
I don't know if There are natural ways to Do this. On Amazon.com there is real human SRD5a1 but very extensive! It could be, that together we get back our good feelings. Maybe.. This Forum helps me a Bit in my Situation. Greetings
Taurine enhances the sexual response and mating ability in aged male rats.
Abstract
It has been demonstrated that taurine is abundant in male reproductive organs, and can be biosynthesized by testis, but the taurine concentration will reduce with aging. The levels of serum LH, T, NOS, and NO were found to be obviously increased by taurine supplementation in aged rats in our previous study. In addition, aging will result in a significant decline in sexual response and function, which may be attributed to the androgen deficiency. Furthermore, NO has been proposed as a crucial mediator of penile erection. That makes us hypothesize that there is potential relationship between taurine decline and erection dysfunction in aged males. So the primary aim of the present study was to investigate the effect of taurine on male sexuality in rats. Taurine was offered in water to male aged (20 months old) rats for 110 days. The effects of taurine on the sexual response, mating ability, levels of serum reproductive hormones, and penile NOS and NO levels were investigated. The results showed that taurine can significantly reduce the EL and ML; obviously increase the ERF, MF, IF, and EJF; stimulate the secretion of GnRH, LH, and T; and elevate penis NOS and NO level in aged rats. The results indicated that taurine can enhance the sexual response and mating ability in aged male rats by increasing the level of testosterone and NO, but the exact mechanism of which needs to be further investigated.