Harmala alkaloid: Difference between revisions

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'''Harmala alkaloids''' are a group of psychoactive alkaloids found primarily within the seeds of [[Harmala_alkaloid#Peganum_harmala_.28syrian_rue.29|''peganum harmala'']], also known as syrian rue.

'''Harmala alkaloids''' are a group of psychoactive alkaloids found primarily within the seeds of [[Harmala_alkaloid#Peganum_harmala_.28syrian_rue.29|''peganum harmala'']], also known as syrian rue. These alkaloids are of interest for their use in Amazonian shamanism, where they are derived from plants. Harmala alkaloids are naturally occurring beta-carboline alkaloids that are structurally related to harmaline, and also found in the vine [[Banisteriopsis caapi]].

==Chemistry==

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==Pharmacology==

Harmala alkaloids are classed as [[MAOIs]]. This means that they inhibit the activity of monoamine oxidase metabolic enzymes of which two varieties exist: MAO-A and MAO-B. The [[alkaloids]] bind reversibly to the active site of the enzyme, inhibiting its endogenous function of destroying amine functions of [[neurotransmitters]] and externally administered centrally active drugs. This has the effect of potentiating and prolonging the central and peripheral activity of both neurotransmitters and a variety of drugs.

Harmala alkaloids are classed as [[MAOIs]]. This means that they inhibit the activity of monoamine oxidase metabolic enzymes of which two varieties exist: MAO-A and MAO-B. The [[alkaloids]] bind reversibly to the active site of the enzyme, inhibiting its endogenous function of destroying amine functions of [[neurotransmitters]] and externally administered centrally active drugs. This has the effect of potentiating and prolonging the central and peripheral activity of both neurotransmitters and a variety of drugs. They are reversible [[MAOIs]] of the MAO-A isoform of the enzyme, and can stimulate the central nervous system by inhibiting the metabolism of monoamine compounds such as serotonin and norepinephrine.

Harmala alkaloids are selective for MAO-A at reasonable doses and bind to the enzyme temporarily, so they are classed as a [[RIMA|reversible inhibitor of monoamine-A]] ([[RIMA]]). At higher doses, they also begin to affect the MAO-B enzyme. Because of the reversible selectivity for MAO-A, harmala alkaloids are considered to be less dangerous in combination with food which contains [[tyramine]] and other substances with monoamine moieties which are reliant on monoamine oxidase for decomposition.

However, it is important to understand that this does not imply that harmala alkaloids will not cause neurotoxicity. Harmala alkaloids temporarily disable the brain's primary mechanism for breaking down [[neurotransmitters]] and drugs which can have negative consequences as material builds up in the [[synapses]], leading to a huge range of downstream central and peripheral effects including [[sedation]], [[stimulation]], [[anxiety]], [[cognitive dysphoria]], [[Physical euphoria|euphoria]], [[headaches]], [[eye strain]], and [[muscle convulsions]].

However, it is important to understand that this does not imply that harmala alkaloids will not cause neurotoxicity. Harmala alkaloids temporarily disable the brain's primary mechanism for breaking down [[neurotransmitters]] and drugs which can have negative consequences as material builds up in the [[synapses]], leading to a huge range of downstream central and peripheral effects including [[sedation]], [[stimulation]], [[anxiety]], [[cognitive dysphoria]], [[Physical euphoria|euphoria]], [[headaches]], [[eye strain]], and [[muscle convulsions]]. The harmala alkaloids are not especially [[Psychedelics|psychedelic]], even at higher dosages, when hypnagogic visions, alongside [[vomiting]] and [[diarrhea]], become the main effect.

Since [[DMT]] is broken down by monoamine oxidase A, inhibition of this enzyme allows for the oral activation of DMT and prolongs the experience for the duration of the harmala alkaloid effects. In combination, harmala alkaloids and DMT are known as [[ayahuasca]].

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-'''Harmala alkaloids''' are a group of psychoactive alkaloids found primarily within the seeds of [[Harmala_alkaloid#Peganum_harmala_.28syrian_rue.29|''peganum harmala'']], also known as syrian rue.
+'''Harmala alkaloids''' are a group of psychoactive alkaloids found primarily within the seeds of [[Harmala_alkaloid#Peganum_harmala_.28syrian_rue.29|''peganum harmala'']], also known as syrian rue. These alkaloids are of interest for their use in Amazonian shamanism, where they are derived from  plants. Harmala alkaloids are naturally occurring beta-carboline alkaloids that are structurally related to harmaline, and also found in the vine [[Banisteriopsis caapi]].
 ==Chemistry==
@@ Line 5: / Line 5: @@
 ==Pharmacology==
-Harmala alkaloids are classed as [[MAOIs]]. This means that they inhibit the activity of monoamine oxidase metabolic enzymes of which two varieties exist: MAO-A and MAO-B. The [[alkaloids]] bind reversibly to the active site of the enzyme, inhibiting its endogenous function of destroying amine functions of [[neurotransmitters]] and externally administered centrally active drugs. This has the effect of potentiating and prolonging the central and peripheral activity of both neurotransmitters and a variety of drugs.
+Harmala alkaloids are classed as [[MAOIs]]. This means that they inhibit the activity of monoamine oxidase metabolic enzymes of which two varieties exist: MAO-A and MAO-B. The [[alkaloids]] bind reversibly to the active site of the enzyme, inhibiting its endogenous function of destroying amine functions of [[neurotransmitters]] and externally administered centrally active drugs. This has the effect of potentiating and prolonging the central and peripheral activity of both neurotransmitters and a variety of drugs. They are reversible [[MAOIs]] of the MAO-A isoform of the enzyme, and can stimulate the central nervous system by inhibiting the metabolism of monoamine compounds such as serotonin and norepinephrine.
 Harmala alkaloids are selective for MAO-A at reasonable doses and bind to the enzyme temporarily, so they are classed as a [[RIMA|reversible inhibitor of monoamine-A]] ([[RIMA]]). At higher doses, they also begin to affect the MAO-B enzyme. Because of the reversible selectivity for MAO-A, harmala alkaloids are considered to be less dangerous in combination with food which contains [[tyramine]] and other substances with monoamine moieties which are reliant on monoamine oxidase for decomposition.
-However, it is important to understand that this does not imply that harmala alkaloids will not cause neurotoxicity. Harmala alkaloids temporarily disable the brain's primary mechanism for breaking down [[neurotransmitters]] and drugs which can have negative consequences as material builds up in the [[synapses]], leading to a huge range of downstream central and peripheral effects including [[sedation]], [[stimulation]], [[anxiety]], [[cognitive dysphoria]], [[Physical euphoria|euphoria]], [[headaches]], [[eye strain]], and [[muscle convulsions]].
+However, it is important to understand that this does not imply that harmala alkaloids will not cause neurotoxicity. Harmala alkaloids temporarily disable the brain's primary mechanism for breaking down [[neurotransmitters]] and drugs which can have negative consequences as material builds up in the [[synapses]], leading to a huge range of downstream central and peripheral effects including [[sedation]], [[stimulation]], [[anxiety]], [[cognitive dysphoria]], [[Physical euphoria|euphoria]], [[headaches]], [[eye strain]], and [[muscle convulsions]]. The harmala alkaloids are not especially [[Psychedelics|psychedelic]], even at higher dosages, when hypnagogic visions, alongside [[vomiting]] and [[diarrhea]], become the main effect.
 Since [[DMT]] is broken down by monoamine oxidase A, inhibition of this enzyme allows for the oral activation of DMT and prolongs the experience for the duration of the harmala alkaloid effects. In combination, harmala alkaloids and DMT are known as [[ayahuasca]].