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Treatment of anxiety, stress, nervousness
Treatment of insomnia
Treatment of muscular aches and pains
Traditionally used in the South Pacific during religious and cultural ceremonies to achieve relaxation and for medicinal purposes
No data exist to quantify risk of adverse effects
ASA recommends stopping herbal supplements as long as 2 wk prior to elective procedures.
Risk of hepatotoxicity, especially when combined with other hepatotoxic drugs
Oversedation when combined with ethanol or other sedative drugs
Potential to affect hemodynamic stability and coagulation
Oral administration: Peak effect 1.8 h, elimination half-life 9 h, metabolized in liver by cytochrome P450.
Effects on various ion channels leading to decreased excitability of CNS.
Enhanced binding and regulation of GABA receptors, leading to anxiolysis, sedation, muscle relaxation, and anticonvulsive effects
Inhibition of limbic system, leading to decreased emotional excitability and mood enhancement
Weak Na channel antagonism, leading to potential anticonvulsant effects
Inhibition of calcium channels, leading to inhibition of vascular smooth muscle
Reduced reuptake of dopamine and norepinephrine
Inhibition of COX, leading to antithrombotic, analgesic, and anti-inflammatory effects
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