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Thread: first cycle..

  1. #1
    crs288 is offline New Member
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    first cycle..

    i was thinking some form of test with maybe winstrol or eq. low dosages of each around 250-275mg/week. start pct 2 weeks after last injection using nolvadex /vitamins/etc.. my question is, i already have my bad days where my face breaks out but here lately its been clear and clearing up well and i want a test that has the is least prone to breakouts (which isnt going to happen)... i know of several different forms of test, test e, test cyp, sust, and so on but what all are the big differences? first cycle btw..
    stats are 6'1'' 205lbs
    maybe 16% bf..
    biceps: 15''
    chest: 42"
    neck: 16"
    forearm: 13"
    thanks in advance guys..

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    kfrost06's Avatar
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    well this is a debatable subject but there is some evidence that shows the shorter ester testosterones like test prop have a lower conversion to estrogen. The estrogen is what will give you the acne. However if you take winstol which is a DHT and acts like an AI that too will inhibit the conversion of the test to estrogen. Also taking proviron will inhibit estrogen and at the same time increas the effectiveness of your test by binding up the SHBG.

    GL

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    Big's Avatar
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    Big is offline Retired~ AR-Hall of Famer ~ "Enforcer"
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    How old are you?

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    Njord is offline Senior Member
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    Quote Originally Posted by kfrost06 View Post
    well this is a debatable subject but there is some evidence that shows the shorter ester testosterones like test prop have a lower conversion to estrogen. The estrogen is what will give you the acne. However if you take winstol which is a DHT and acts like an AI that too will inhibit the conversion of the test to estrogen. Also taking proviron will inhibit estrogen and at the same time increas the effectiveness of your test by binding up the SHBG.

    GL
    Where have you heard this? The closest I found was in AR's book where he states "Winstrol has been speculated to have anti-progestenic properties". I would not count on winstrol to help with estrogen control during cycle personnally.

    The key in my opinion to control sides is to keep blood plasma levels as stable as possible. This means ed injections for prop and phenyl prop (including sustanon ) and 2x week for Enth and Cyp.

    You can also keep estrogen related sides down by controlling your estrogen with a SERM or AI while on cycle. I have never used them while on, so can't really help you there.

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    crs288 is offline New Member
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    im 20 years old... i dont want to overkill the first time, i had read that some people respond well to low doses so why build tolerance off the start thats why i said 250mg/week but im open to more suggestions..if i took clomid or nolva during cycle would that help with the estrogen or is there another route?... thanks guys!

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    too young dood

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    Quote Originally Posted by kfrost06 View Post
    Originally Posted by kfrost06
    well this is a debatable subject but there is some evidence that shows the shorter ester testosterones like test prop have a lower conversion to estrogen. The estrogen is what will give you the acne. However if you take winstol which is a DHT and acts like an AI that too will inhibit the conversion of the test to estrogen. Also taking proviron will inhibit estrogen and at the same time increas the effectiveness of your test by binding up the SHBG.

    GL

    Quote Originally Posted by Njord View Post
    Where have you heard this? The closest I found was in AR's book where he states "Winstrol has been speculated to have anti-progestenic properties". I would not count on winstrol to help with estrogen control during cycle personnally.

    The key in my opinion to control sides is to keep blood plasma levels as stable as possible. This means ed injections for prop and phenyl prop (including sustanon ) and 2x week for Enth and Cyp.

    You can also keep estrogen related sides down by controlling your estrogen with a SERM or AI while on cycle. I have never used them while on, so can't really help you there.
    Well, I didn't hear it, I read it. Here's one of countless studies...

    http://cancerres.aacrjournals.org/cg...ment/3378s.pdf

    Comparative Studies of Aromatase Inhibitors in Cultured Human Breast
    Cancer Cells1


    The presence of aromatase activity, estrogen receptors, and
    estrogenic responsiveness in MCF-7 human breast cancer
    cells has allowed this cell line to be used as a unique in vitro
    system for investigating the biological activities of potentially
    therapeutic aromatase inhibitors. We now report the results of
    studies which have examined the cytotoxicity, antiaromatase,
    and intrinsic estrogenic activities of
    aminoglutethimide, 1,2-
    dehydrotestolactone (testolactone), dihydrotestosterone, 4-hydroxy-
    4-androstene-3,17-dione, and 10-propargylestr-4-ene-
    3,17-dione within MCF-7 monolayer cultures. Cell viability was
    determined by trypan blue exclusion, and aromatase activity
    was assessed by quantifying the amounts of [3H]estradiol
    formed from [3H]testosterone . Estrogenic activity was assessed
    by examining the ability of each inhibitor to increase cytoplasmic
    progesterone receptor and deplete cytoplasmic estrogen
    receptor concentrations in these cells during a 5-day incuba
    tion period. Cytoplasmic progesterone and estrogen receptors
    were measured by the single-saturating-dose technique using
    [17a-metfjy/-3H]-17a,21 -dimethyl-19-norpregna-4,9-diene-
    3,20-dione and [3H]estradiol as the labeled ligands for each
    assay, respectively. The results showed that all of these com
    pounds were noncytotoxic aromatase inhibitors in MCF-7 cells
    but that these agents demonstrated marked differences in
    inhibitory potency
    (10-propargylestr-4-ene-3,17-dione > 4-hydroxy-
    4-androstene-3,17-dione :»dihydrotestosterone » tes
    tolactone = aminoglutethimide). The incubation of cells with 4-
    hydroxy-4-androstene-3,17-dione resulted in cytoplasmic pro
    gesterone and estrogen receptor responses that were similar
    in magnitude to those observed in other cultures incubated
    with equimolar concentrations of estradici. None of the other
    four agents demonstrated estrogenic activity in this system.
    However, we have previously observed that dihydrotestoster
    one has substantial antiestrogenic action in this system
    . Taken
    together, these results indicate that some aromatase inhibitors
    may influence the hormonal regulation of human breast cancer
    cells by more than one mechanism.


    DHTs, e.g. winstrol, proviron, masteron all act as AIs furthermore you don't control your estrogen pruduction with a SERM, it is used to compete with your estrogen not inhibit it's production.

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