Dianabol 8R,9S,10S,13S,14S,17S-17-hydroxy-10,13
An Overview of Anabolic‑Androgenic Steroids (AAS)
> Disclaimer: This document is intended solely for educational purposes and does not endorse or encourage the use of anabolic‑androgenic steroids (AAS). All information is provided in a neutral, factual manner.
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1. What Are AAS?
Feature | Description |
---|---|
Chemical class | Steroid hormones derived from cholesterol; modified to increase androgenic activity and reduce metabolism. |
Common examples | Testosterone (base form), Nandrolone decanoate, Oxymetholone, Stanozolol, Boldenone undecylenate. |
Mechanism of action | Bind to intracellular androgen receptors → modulate gene transcription → promote protein synthesis and cell proliferation. |
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2. Historical Context
- Early 20th Century: http://voicebot.digitalakademie-bw.de:3000/moelauna531579 Discovery of testosterone (1919) and its isolation.
- 1950s–1960s: Development of anabolic agents for medical use (e.g., treating muscle wasting).
- 1970s–1980s: Emergence in sports; first major doping scandals.
3. Prevalence in Sports
Sport | Estimated Anabolic Agent Use (%) |
---|---|
Professional Cycling | 20–30% |
Bodybuilding | >50% (muscle hypertrophy focus) |
Basketball | ~10% |
Football (Soccer) | <5% |
Data from WHO and anti-doping agencies; note that underreporting is significant.
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4. Biological Impact
- Muscle Protein Synthesis: Enhanced via activation of mTOR pathway.
- Recovery Time Reduction: Decreased protein degradation, faster glycogen replenishment.
- Hormonal Alterations: Elevated testosterone analogues can lead to negative feedback suppression of endogenous production.
5. Clinical Implications
- Performance Enhancement
- Risk of Adverse Events
- Regulatory Concerns
6. Recommendations
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