Exam 4 - Herbal medicines and natural treatments Flashcards

1
Q

Do herbal medicines have to be tested? What do companies have to do because of this?

A
  • no
  • cannot market it as a treatment for a specific disorder (anxiety = calming)
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2
Q

St. John’s Wort

A
  • hypericin and hyperforin active ingredients
  • “provide emotional balance”, primarily used for treatment of depression
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3
Q

Pharmacokinetics of St. John’s Wort

A
  • active ingredients interfere w/ liver enzymes, can either increase or decrease level of metabolization of drugs
  • peak levels reached in 5 hours
  • half life is 25 hours
  • can result in adverse effects when combine w/ other drugs
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4
Q

Pharmacodynamics of SJW

A
  • mechanism not clear
  • inhibits MAO inhibition but only at high concentrations
  • bind to GABA, benzo and NMDA receptors
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5
Q

Clinical efficacy of SJW

A
  • MAYBE effective in treating MILD depression
  • however, 2 large studies showed that it was no more effective than placebo
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6
Q

Side effects of SJW

A
  • photosensitivity in fair skinned people
  • some psychoactive properties found in mother’s milk
  • may precipitate hypomanic state
  • if used with SSRIs, may cause serotonin syndrome
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7
Q

Ginkgo

A
  • Egb-761
  • “mental sharpness”, alleviate symptoms associated w/ range of cognitive disorders
  • contains flavonoids (interfere w/ liver enzymes), and terpenoids (interfere w/ clotting factors)
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8
Q

Pharmacokinetics of Ginkgo

A
  • readily absorbed, peak concentrations around 2-3 hours
  • mech of elimination not known
  • half life is 5 hours
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9
Q

Pharmacodynamics of Ginkgo

A
  • contains compounds thought to provide membrane protection and neurotransmission modulation
  • increased alpha wave activity, indicative of increased altertness (similar to drinking a coffee)
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10
Q

Clinical efficacy of Ginkgo

A
  • modest effects on cognitive functioning associated w/ cerebrovascular impairments
  • benefit may be solely to due its action to reduce stickiness of blood platelets
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11
Q

Side effects of Ginkgo

A
  • headache and GI upset
  • can cause spontaneous bleeding an hemorrhaging
  • safety in pregnancy has not been established
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12
Q

Kava

A
  • similar to alcohol and sedative hypnotics
  • root of Kava plant
  • induces relaxation, social interaction, sleep and sociocultural life
  • used to therapy for anxiety
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13
Q

Pharmacokinetics of Kava

A
  • pharmacological action due to kava lactones
  • well absorbed
  • inhibits cytochrome P450 liver enzymes, potentially increasing blood concentrations and toxicity of drugs
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14
Q

Pharmacodynamics of Kava

A
  • bind to either GABA or benzo binding sites
  • anticonvulsant and muscle relaxant properties
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15
Q

Clinical effects of Kava

A
  • anxiolytic effect at 70 mg
  • high doses induces feeling of well being, drowsiness, sedation and feeling of intoxication
  • effective for short-term treatment of mild-mod anxiety
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16
Q

Side effects of Kava

A
  • drowsiness, nausea, muscle weakness, blurred vision, jaundice
  • should not be taken with alcohol, benzos, barbiturates, THC, or other CNS depressants
  • should only be used short-term, can cause hepatotoxicity
17
Q

Ephedrine

A
  • naturally occurring psychoactive substance sound in ephedra sinica
  • releases epi, norepi, and dopa
  • resembles amphet
  • increases BP, HR
18
Q

Omega-3 Fatty Acids

A
  • include EPA and DHA
  • found in ocean fish
19
Q

Use of Omega-3 Fatty Acids during pregnancy

A
  • required for normal fetal development - neural and retinal tissue growth
  • may help or prevent depressive symptoms
20
Q

Use of Omega-3 Fatty Acids in children and adolescents

A
  • efficacy shown in autism spectrum disorder, reduction of allergy risks, and in developmental behaviors
  • results mixed for ADHD
  • may be beneficial in subthreshold psychosis
21
Q

Antidepressant and Omega-3 Fatty Acids use

A
  • use in BPD is well supported
  • can reduce depressive symptoms
22
Q

Cardiovascular effects of Omega-3 Fatty Acids

A
  • reducing risk of CV deaths
  • reduces platelet adhesion (heart attacks and strokes)
  • benefits on triglycerides
23
Q

Omega-3 and Dementia risk

A
  • DHA may:
    • reduce incidence of dementia
    • prevent cognitive decline
    • improve synaptic and NT functioning
    • enhance learning and memory performances
  • display neuroprotective properties
24
Q

Valerian

A
  • mild sedative and anxiolytic
  • may affect GABA receptors by acting like a mild benzo
  • side effects: liver toxicity, headaches, excitability/uneasiness
  • potential interaction w/ SSRIs
25
Q

Evening primrose

A

promoted for treatment of schizo and ADHD

26
Q

Hops

A
  • sedative-hypnotic agent, promoted to treat either insomnia or anxiety
27
Q

Lemon balm/passion flower/skullcap

A

though to posses CNS sedative properties, promoted as sedatives and anxiolytics