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MASSIVE MUSCLES WITHOUT THE SIDE EFFECTS
THE NEW ERA IN BODYBUILDING AND SPORTS PERFORMANCE IS USING SELECTIVE ANDROGEN RECEPTOR MODULATORS (SARMS), BETTER GAINS WITHOUT HARMFUL SIDE EFFECTS.
SARMS WORKS BY SELECTIVELY TARGETING ANDROGEN RECEPTORS IN MUSCLES AND BONES WITHOUT EFFECTING HORMONE LEVELS.
ANDROGEN RECEPTOR (AR) IS A MEMBER OF THE STEROID RECEPTOR SUPER-FAMILY AND PLAYS AN IMPORTANT ROLE IN SEVERAL BIOLOGICAL PROCESSES SUCH AS THE DEVELOPMENT AND MAINTENANCE OF THE SECONDARY SEXUAL ORGANS, BONE, MUSCLE AND OTHERS. THERE IS ONLY ONE ANDROGEN RECEPTOR AND IT IS PRESENT EVERYWHERE IN OUR BODY, BONES, MUSCLE, LIVER, ORGANS, SKIN, TENDONS, LIGAMENTS, PROSTATE, REPRODUCTIVE AND CENTRAL NERVOUS SYSTEMS. THE BIOLOGICAL PROCESSES ARE TYPICALLY CATEGORISED AS ANDROGENIC (THE EFFECTS ON SECONDARY SEX ORGANS) OR ANABOLIC (THE EFFECTS ON MUSCLE AND BONE). NONSTEROIDAL RECEPTOR MODULATORS (SERMS, SARMS ETC) ACT AS TISSUE SELECTIVE ANGONISTS AND/OR ANTAGONISTS VIA THEIR RESPECTIVE RECEPTOR AND PROVIDE A UNIQUE AND TISSUE-SELECTIVE PHARMACOLOGIC APPROACH TO MUSCLE BUILDING WITHOUT THE SIDE EFFECTS OF STEROIDS.
POSSIBLE SIDE EFFECTS OF STEROIDS FOR MEN INCLUDE; LOSS OF HAIR, GYNECOMASTIA (BITCH TITS), INCREASED ANGER (ROID RAGE), DECREASED SEXUAL PERFORMANCE, TESTICULAR SHRINKAGE AND POSSIBLE SHUT DOWN. FOR WOMEN, THE SIDE EFFECTS CAN INCLUDE; INCREASED FACIAL HAIR, MENSTRUAL CYCLE CHANGES, DEEPENED VOICE, BREAST REDUCTION, PATTERN BALDNESS, CLITORIS ENLARGEMENT AND FOR BOTH MEN AND WOMEN INCLUDE; SKIN DISEASE, CARDIOVASCULAR DISEASE, LIVER AND KIDNEY DISEASE AND PSYCHOLOGICAL EFFECTS.
THE MOST EFFECTIVE SARMS FOR MUSCLE BUILDING IS S-22. EXPERIMENTAL EVIDENCE HAS BEEN PRODUCED SHOWING S-22'S TISSUE SELECTIVITY BY ACTIVATION OR REPRESSION OF GENOMIC AND NON-GENOMIC SIGNAL TRANSDUCTION PATHWAYS THAT ARE DISTINCT FROM THOSE UTILIZED BY DHT. MALE RATS TREATED FOR 14 DAYS WITH 1MG/DAY S-22 SHOWED INCREASED SIDE MUSCLE WEIGHT BUT SIGNIFICANTLY REDUCED PROSTATE WEIGHT, DEMONSTRATING THE TISSUE SELECTIVITY OF S-22. AS IN VIVO STUDIES WITH S-22 USING INTACT MALE RATS SHOWED A REDUCTION IN PROSTATE SIZE, WE SPECULATED THAT IT WOULD INHIBIT LNCAP (PROSTATE CELL GROWTH).
FIGURE E SHOWS THAT S-22 RETARDED LNCAP CELL GROWTH, INDICATING THAT S-22 IS SELECTIVELY ANABOLIC, PROMOTING BONE CELL AND MUSCLE GROWTH BUT NOT PROSTATE OR PROSTATE CANCER CELL GROWTH. (STEROIDAL ANDROGENS AND NONSTEROIDAL, TISSUE SELECTIVE ANDROGEN RECEPTOR MODULATORS (SARM), S-22, REGULATE ANDROGEN RECEPTOR FUNCTION THROUGH DISTINCT GENOMIC AND NON-GENOMIC SIGNALING PATHWAYS) SEPT 18 2008
AS SARM'S S22 IS EQUIVALENT TO THAT OF DHT IN STRENGTH AND RESULT BUT WITHOUT THE SIDE EFFECTS RELATED TO STEROIDS AND DHT IS 3 TIMES STRONGER THAN TESTOSTERONE PROPIONATE, IT FOLLOWS THAT SARM'S S22 IS 3 TIMES STRONGER AND MORE EFFECTIVE THAN TESTOSTERONE PROPIONATE (THE STRONGEST STEROID).
BOTH MEN & WOMEN BENEFIT FROM SARMS S22
SARMS S22 - 3 TIMES MORE EFFECTIVE THAN TESTOSTERONE PROPIONATE AND NO ADVERSE SIDE EFFECTS. MORE MASS & STRENGTH (NO FAT OR PUFFINESS) AND NO NEED TO CYCLE WITH MINIMAL TO NO MASS LOSS. NOTE: SARMS S22 IS POSSIBLY DETECTABLE BY BLOOD AND URINE TESTS FOR 72 HOURS.Leave a comment:
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A friend of mine who does MMA went to a sports doctor here and the fucking guy put him on SARMS s22 and told him that it will be the best thing he's ever taken in his life. He said no sides, no estrogen issues, etc..
Let me dig up some literature and I'll post it later. Going to the gym now.Leave a comment:
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