Boldenon Nebenwirkungen Frauen

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    boldenon nebenwirkungen frauen Mitglieder in diesem Forum: Portal Forum Videos Galerie my. Boxen Ziel Gewicht kg: Schon wegen der Progestron Wirkung des Nandrolons. Hinzu kommen noch die rauen Mengen Testo. - Die Fitness & Bodybuilding Community | Training, Supplements, Diät, Steroide

    boldenon nebenwirkungen frauen

    Mitglieder in diesem Forum: Portal Forum Videos Galerie my. Boxen Ziel Gewicht kg: Schon wegen der Progestron Wirkung des Nandrolons. Hinzu kommen noch die rauen Mengen Testo. Clomid,Zink,vitamin E und eventulle phyto hypophyson L einsetzten. Wie bei einem Kurbelmotor muss man da vielleicht etwas nachhelfen.

    Ab dem Monat wird sich der testospiegel wider im Normbereich befinden. So in Monaten wirst du wider voll Saft sein Einfach die Geduld nicht verlieren Steht denn Famileinplanung an??? Aber bei mg testo und mg Deca kann man sicher sein dass sich 0 Spermien im Ejakulat befinden.. Ich glaube das Zeug wird Ment heissen? Es ist ein Nortestosteron Derivat. Klingt ja interessant, vor allem wie die ins hormonsystem eingreifen wollen ohne was am endogenen testo zu versauen.

    I MENT has always been my favourite steroid, and that's just from reading the studies and looking at the structure of it. Thinking of what MENT can do should make every steroid user drool. This stuff is nearly as strong as its alpha-alkylated counterpart mibolerone cheque drops but without the mad liver toxicity. It's a 19Nor substance, a nandrolone derivative. Its very much like nandrolone, except it has a 7-alpha-methyl attachment.

    This attachment stops it from being 5-alpha-reduced1. Now as you know, 5-alpha-reduction makes nandrolone, otherwise a very potent hormone, much weaker. But because of trenbolone's triple double bond structure, it also does not aromatize. But MENT on the other hand is still capable of aromatizing2 which would not be the case with a 4 or 5 methylation , so you still have the benefits of estrogen: Its estrogenic potency may in fact be slightly larger because 7-alpha-methyl-estradiol the product of MENT aromatization may show less affinity to binding proteins as well.

    It is in fact suggested that part of MENT's actions may be the result of this potent estrogen1. This stuff should literally and in all aspects be stronger than testosterone. Its androgenic character will be like trenbolone same risk of hair loss, prostate hypertrophy, acne, deepening of voice and its estrogenic character will be like that of nandrolone same risk of gyno, bloating and fat gain.

    But its hypertrophic ability should be much higher than either of these, or even testosterone. One question begs to be asked however: In depot shots that means daily injections. This is after all the same company that is looking to market injectable testosterone undecanoate for shots once every 10 weeks. Well, so far two uses have been found for MENT in the medical community. Sundaram, who is probably the leading researcher where nandrolone and its derivatives are concerned, found it to be of perfect use for both replacment therapy for men, as well as for male contraception3 Which would suggest it at least doesn't suffer from the libido suppressing drawback that nandrolone does.

    And from what the latest research in the matter seems to suggest, it looks like Schering is planning on making it in implant pellets4 that would release the drug over time, with 4 pellets delivering no more than 1. Assuming most of us do not want to use pellets that could pose a problem for the use of MENT for enhancement purposes, lest there are some black market knock-offs.

    But take it from one who had looked, currently none of the wholesalers seem to have access to MENT. So the pending release of MENT may not be such joyful news after all except for Schering who stands to profit nonetheless. There is one study5 in particular that documented the exact effects of MENT very well, although it was carried out on castrated mice so these effects may not be transcribed to humans. What was also interesting was that MENT did not seem to stimulate aggressive behaviour at all.

    Compared to a control group of castrated mice, there levels of aggression did not nominally increase at all. This could be positive news for all those roid ragers out there giving the steroid community a bad name. Another interesting study6 more or less quantified the effects of MENT as compared to testosterone, and found that its androgenic character, based on the weights of ventral prostate and seminal vesicles, was 4 times greater than that of testosterone and that the hypertrophic nature was no less than 10 times greater, based on the weight increase in the levator ani muscle.

    More disturbing was the finding that the suppressive effect of MENT on HPTA was 12 times greater than that of testosterone, which is concerning at the least for a product with uses as a male contraceptive. The varying figures indicate that where a dose of testosterone that can maintain serum gonadotropin levels and muscle mass, can also maintain the prostate and seminal vesicles, where MENT cannot.

    This can easily be explained because the larger part of testosterones androgenic action stems from target specific conversion to a more androgenic form in the prostate and other androgen sensitive tissues, because these have a high concentration of 5-alpha-reductase.

    But MENT is not affected by 5-alpha-reductase. On the one hand that is why it is such a strong hormone compared to testosterone estimated 3 times stronger , but also why its half-life is shorter begging daily injections still with the acetate ester.

    So in conclusion we can state that this hormone is extremely powerful at what it does and could find more uses, both in the medical community to treat wasting diseases and burns and in the sports enhancement field. While its production is imminent and its safety record proven in both studies with humans and animals, it remains to be seen for what purpose and in what form it will be marketed by Schering.

    As things are now, it looks like it will be produced in a form that will only be useful in hormonal replacement therapy, and not in short term treatment of burns or wasting diseases, or for sports enhancement.

    This information is of course purely hypothetical and based on an injectable version of the aforementioned acetate ester of MENT. Given the short half life and the short ester, daily injections would be required. Similar results could be obtained with mg per day of MENT. The drug does aromatize like nandrolone, and it aromatizes to 7-alpha-methyl-estradiol. In light of the low affinity of MENT for binding proteins, the same could be assumed of 7-alpha-methyl-estradiol, so this may be a quite potent estrogen.

    Combined with the progestagenic action of 19Nor steroids that could lead to a reasonable risk for gynocomastia. Especially those prone to estrogen should probably supplement with 1 mg per day of arimidex or 2. If stacked with additional aromatizing or otherwise estrogenic hormones its best to keep Nolvadex on hand as well, and to remind yourself of the progestagenic action.

    RU, the abortion drug, is the only known truly effective progestin blocker, but is hard to find and terribly expensive. Combining with Winstrol may help, as it does have some competitive progestagenic blocking abilities, but their extent is not quantified in any study.

    The androgenic effects may be quite strong, so acne probably will occur, and men prone to problems with male pattern hair loss or prostate problems should be cautious. Due to the 7-alpha-methyl group, MENT is not affected by 5-alpha-reductase, so treatments like Proscar will have no effect.

    When stacking this product, one will probably be looking to add mass to the frame. It would not make a very good match for nandrolone, as nandrolone can be considered the weaker relative of MENT, with similar action but much less androgenic possibilities. Keep in mind that there are very few real world results with MENT on humans, and there is no literal data on its hypertrophic ability, so a lot of this is hypothetical, based on the available studies and evidence.

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