Trenbolone Enanthate is a synthetic derivative of Dihydrotestosterone, displaying a potent androgenic effect that is responsible for increases in muscle density and hardness and a moderate anabolic effect that creates a positive nitrogen balance in humans and promotes protein synthesis.
Since SP Trenbolone Enanthate is a derivative of Dihydrotestosterone, Trenbolone does not aromatize at any dosage and thus it cannot be converted into estrogen. Therefore, estrogen-related water retention is eliminated. Furthermore, Trenbolone Enanthate has the longer acting enanthate form.
- That notwithstanding, Dermatological/integumental: oily skin, acne vulgaris, acne conglobata, seborrhea, stretch marks (due to rapid muscle enlargement), hypertrichosis (excessive body hair growth), androgenic alopecia (pattern hair loss; scalp baldness), fluid retention/edema.
- Reproductive/endocrine: libido changes, reversible infertility, hypogonadotropic hypogonadism.
- Male-specific: spontaneous erections, nocturnal emissions, priapism, erectile dysfunction, gynecomastia (mostly only with aromatizable and hence estrogenic AAS), oligospermia/azoospermia, testicular atrophy, intratesticular leiomyosarcoma, prostate hypertrophy, prostate cancer.
- Again, Female-specific: masculinization, irreversible voice deepening, hirsutism (excessive facial/body hair growth), menstrual disturbances (e.g., anovulation, oligomenorrhea, amenorrhea, dysmenorrhea), clitoral enlargement, breast atrophy, uterine atrophy, teratogenicity (in female fetuses).
- Child-specific: premature epiphyseal closure and associated short stature, precocious puberty in boys, delayed puberty, and contrasexual precocity in girls. jungle boys seeds
- Psychiatric/neurological: mood swings, irritability, aggression, violent behavior, impulsivity/recklessness, hypomania/mania, euphoria, depression, anxiety, dysphoria, suicidality, delusions, psychosis, withdrawal, dependence, neurotoxicity, cognitive impairment.
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- Still, Musculoskeletal: muscle hypertrophy, muscle strains, tendon ruptures, rhabdomyolysis.
- Still, Cardiovascular: dyslipidemia (e.g., increased LDL levels, decreased HDL levels, reduced apo-A1 levels), atherosclerosis, hypertension, left ventricular hypertrophy, cardiomyopathy, myocardial hypertrophy, polycythemia/erythrocytosis, arrhythmias, thrombosis
- Again, Hepatic: elevated liver function tests (AST, ALT, bilirubin, LDH, ALP), hepatotoxicity, jaundice, hepatic steatosis, hepatocellular adenoma, hepatocellular carcinoma, cholestasis, peliosis hepatis; all mostly or exclusively with 17α-alkylated AAS.
- Renal: renal hypertrophy, nephropathy, acute renal failure (secondary to rhabdomyolysis), focal segmental glomerulosclerosis, renal cell carcinoma.
- Moreover, Others: glucose intolerance, insulin resistance, immune dysfunction.
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