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12-30-2004, 06:21 PM #1
what is cytadren (aminoglutethimide)
anyone hear of this ****, my bro wants me to get him some but i have no clue what is is or whats its for. help a brotha out lol
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12-30-2004, 06:26 PM #2
inhibits cortisol....helps out with cycle,makes it more effective at lower doses
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12-30-2004, 06:28 PM #3VET Retired
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It's a drug that inhibits your bodys natural hormonal output. I would not use it that's for sure.
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12-30-2004, 06:30 PM #4
I'd stay away from it too it has it's sides....
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12-30-2004, 06:31 PM #5VET Retired
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Originally Posted by K$I$N$G$P$I$N
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12-30-2004, 06:31 PM #6
anabolics 2004
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12-30-2004, 06:32 PM #7
If william Llewellyn is wrong I'll erase my post
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12-30-2004, 06:35 PM #8
"research was bare as to the best way to use it as a cortsol lowering anti-catabolic"
william Llewellyn
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12-30-2004, 06:38 PM #9VET Retired
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Llewellyn, Auther.l.Rea, Palumbo all make mistakes especially Palumbo. Do your own research, up to the other day I found a mistake, a huge one at that in one of Llewellyns' articles in MD.
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12-30-2004, 06:39 PM #10Originally Posted by big k.l.g
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12-30-2004, 06:43 PM #11VET Retired
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Originally Posted by K$I$N$G$P$I$N
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12-30-2004, 06:45 PM #12
k guys, thanks, ill let my bro know. i wouldnt touch the sh-t after hearing what you guys are saying about it
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12-30-2004, 06:45 PM #13Originally Posted by big k.l.g
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12-30-2004, 09:27 PM #14Originally Posted by big k.l.g
Inhibition of desmolase -- the undesired side effect of Cytadren -- will lead, at least temporarily, to decreased production of cortisol. Contrary to the other claims, there is no evidence, nor good reason to believe, that reducing cortisol below normal would be of benefit to the weight training athlete, and considerable evidence that it is a bad idea.
It is claimed that Cytadren significantly inhibits natural production of testosterone . That is a fallacy.
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12-30-2004, 09:31 PM #15Originally Posted by Narkissos
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12-31-2004, 03:37 AM #16Originally Posted by K$I$N$G$P$I$N
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12-31-2004, 09:23 AM #17VET Retired
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Originally Posted by Narkissos
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12-31-2004, 10:58 AM #18Originally Posted by big k.l.g
Where you training for the New year Bro?
I think i'm sticking to C.O.B.
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12-31-2004, 11:48 AM #19Originally Posted by jcstomper
BassMuscle
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12-31-2004, 11:59 AM #20VET Retired
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Originally Posted by BassMuscle
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12-31-2004, 12:39 PM #21Originally Posted by Stout1
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12-31-2004, 06:33 PM #22Originally Posted by big k.l.g
BassMuscle
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12-31-2004, 06:44 PM #23
General info: http://www.drugs.com/PDR/Remeron_Tablets.html
This study is on depressed patients.
"Mirtazapine Attenuates Hypothalamic-pituitary-adrenocortical Axis Hyperactivity in Depressed Patients"
A DGReview of :"Attenuation of hypothalamic-pituitary-adrenocortical hyperactivity in depressed patients by mirtazapine"
Psychopharmacology
04/17/2003
By Anne MacLennan
German clinicians have found that mirtazapine rapidly attenuates the dysregulation of the hypothalamic-pituitary-adrenocortical (HPA) system seen in depressed patients.
They note, however, that this effect of mirtazapine is not necessarily related to clinical improvement.
Previous research suggested that dysregulation of the HPA system might play an important role in the pathophysiology of depression, and that normalization of HPA axis hyperactivity precedes successful treatment with antidepressants, write Dr. Cornelius Schüle and colleagues at the Department of Psychiatry at University of Munich.
Previous studies demonstrated that mirtazapine acts as an antagonist at presynaptic beta 2 receptors and at post-synaptic 5-hydroxytryptamine (5-HT) and histamine H1 receptors. In addition, it has been shown to have an acute inhibiting effect on cortisol secretion in healthy subjects.
Dr. Schüle and colleagues investigated whether mirtazapine might reduce HPA axis hyperactivity in patients with depression, and whether this is related to treatment outcome.
They enrolled 40 patients who met Diagnostic and Statistical Manual - Revision IV criteria for a major depressive episode, and who were treated with mirtazapine 45 mg daily for 5 weeks. The combined dexamethasone suppression/corticotropin releasing hormone stimulation (DEX/CRH) test was carried out 1 week before and 1 week after the start of mirtazapine treatment.
The clinicians found that mirtazapine effectively reduced the overshoot of cortisol and adrenocorticotropin in the DEX/CRH test in the first week among patients who either responded or did not respond to treatment.
Dr. Schüle and colleagues conclude, "Apparently, mirtazapine rapidly attenuates HPA axis hyperactivity in depressed patients via direct pharmaco-endocrinological effects. However, this amelioration of HPA system dysregulation is not necessarily related to clinical improvement."
Psychopharmacology 2003;166:271-275.
This is on Healthy ones
Effects of mirtazapine on growth hormone , prolactin, and cortisol secretion in healthy male subjects.
Laakmann G, Schule C, Baghai T, Waldvogel E.
Psychiatrische Klinik, Ludwig Maximilians Universitat, Munchen, Germany. [email protected]-muendren
In the present study the effects of acute PO-administration of 15 mg mirtazapine on the growth hormone (GH), prolactin (PRL), and cortisol (COR) secretion were examined in eight physically and mentally healthy male subjects, compared to placebo. Mirtazapine is a new antidepressant agent which does not inhibit the reuptake of norepinephrine or serotonin but is an antagonist of presynaptic and, presumably, postsynaptic alpha 2-receptors as well as an antagonist of postsynaptic 5-HT2 and 5-HT3-receptors. After insertion of an i.v. catheter, blood samples were drawn 1 h prior to the administration of mirtazapine or placebo, at time of application, and during the time of 4 h after application in periods of 30 min. Plasma concentrations of GH, PRL, and COR were determined in each blood sample by double antibody RIA methods. The area under the curve (AUC) value was used as parameter for the GH, PRL, and COR response. With respect to GH and PRL secretion, mirtazapine did not show any effects in comparison with placebo. However, in all subjects, the COR concentrations were remarkably lower after mirtazapine compared to placebo, the difference being obvious in the mean value graphs 60 min after the application up to the end of the measurement period. The t-test for paired samples revealed a highly significant difference (P < 0.01) in COR-AUC-values between the mirtazapine group (mean COR-AUC: 1558.07 micrograms/100 ml x 240 min) and the placebo group (mean COR-AUC: 2698.86 micrograms/100 ml x 240 min). Further studies have to elucidate the question whether the demonstrated inhibition of COR secretion after application of 15 mg mirtazapine is caused by central or peripheral effects of this substance.
Hope this helps.
BassDemon
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12-31-2004, 06:52 PM #24VET Retired
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Yeah thanks Bro looks like it may have potential in PCT. I'll have to find some time to research it more.
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01-16-2005, 12:40 PM #25VET Retired
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Originally Posted by johan
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01-16-2005, 01:07 PM #26VET Retired
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Ok thanks alot for the heads-up!
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01-17-2005, 11:59 AM #27Originally Posted by johan
My friend takes 1/3 of the tablet, thats about 10mg daily and has no problems with it. And on the study that I posted for healthy people they only took 15mg daily, but it doesn't say anything about sides.
BassMuscle
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01-17-2005, 02:45 PM #28
My friend never had any sides that I know about, hasn't complained.
I may try it at the end of my cycle by april, I'll post sides and benefits of Remeron.
BassMuscle
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