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Mechanism of action: Clenbuterol is a bronchodilator from rough selective beta 2-adrenoceptors. Removes bronchial spasms and has sekretolitichno action, stechnyava viscous secretions and facilitates their excretion. Causes relaxation of cerebral blood vessels but also vessels of skeletal muscle. It turns tocolytic effect. Adverse pharmacological effects of clenbuterol are due to weak activation of beta-1-adrenortseptorite heart - has positive inotropic and chronotropic effect. Bronhospazmolitichniyat effect is prolonged and dose-dependent. At doses that exceed therapeutic repeatedly, clenbuterol is not significantly affected heart rate and blood nalyagene cardiotoxic and does not cause change. Clenbuterol has a pronounced thermogenic effect and imma pronounced anabolic effect. All beta-2 agonists including their D-and L-isomers are prohibited. As an exception, formoterol, salbutamol, salmeterol and terbutaline when
administered by inhalation, require an abbreviated Therapeutic Exception uses. Notwithstanding the issue of any kind in a Therapeutic use a concentration of salbutamol (free plus glucuronide) exceeding 1000 ng / mL, will be considered an Adverse Analytical Finding unless the athlete proves that the abnormal result was the consequence of therapeutic use of inhaled salbutamol.

Name: clenbuterol hydrochloride
Trade names: Clenbuterol
Category: Beta-2-agonist
Type: oral
Action time: 6-8 hours
Optimal dosage:    0,04 – 0,08 mcg
Common side effects: muscle cramps, arrhythmias, nervousness, tremor, high body temperature, headache, spasm of the bronchi