2006
DOI: 10.1016/j.euroneuro.2005.08.005
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Antidepressant-like effect of harmane and other β-carbolines in the mouse forced swim test

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Cited by 138 publications
(106 citation statements)
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“…To our knowledge, the use of AYA in a controlled clinical setting in patients with current depression --or in any other clinical population --has never been investigated. Moreover, the results of the present study, although preliminary, are corroborated by mounting research showing antidepressive potentials for AYA alkaloids in nonhuman animals [16][17][18][19][20][21][22][23][24] and in humans. 13,25,26 Finally, the reported results may prompt novel research into substances with faster therapeutic actions than currently available pharmacological resources, thus making antidepressive treatment more effective.…”
Section: Discussionsupporting
confidence: 71%
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“…To our knowledge, the use of AYA in a controlled clinical setting in patients with current depression --or in any other clinical population --has never been investigated. Moreover, the results of the present study, although preliminary, are corroborated by mounting research showing antidepressive potentials for AYA alkaloids in nonhuman animals [16][17][18][19][20][21][22][23][24] and in humans. 13,25,26 Finally, the reported results may prompt novel research into substances with faster therapeutic actions than currently available pharmacological resources, thus making antidepressive treatment more effective.…”
Section: Discussionsupporting
confidence: 71%
“…4,5 Studies conducted in rodents by our group and by others using doses of 10-15 mg/kg harmine have demonstrated antidepressive effects for this compound, which were associated with increases in BDNF levels. 17,19,21 Furthermore, harmine, THH, and harmaline are potent natural, selective, reversible, and competitive inhibitors of the MAO enzyme, especially of the MAO-A subtype. 9,36 THH acts as a selective serotonin reuptake inhibitor as well as an MAOI.…”
Section: Discussionmentioning
confidence: 99%
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“…The whole plants of P. harmala have also been used as folk medicine in Turkey and Iran (Hemmateenejad et al, 2006;Kartal et al, 2003). Pharmacological studies on extracts and alkaloids separated from P. harmala have shown some biological activity and pharmacological effects, such as anti-tumor and analgesic effects Sobhani et al, 2002;Farouk (wileyonlinelibrary.com) DOI 10.1002/bmc.3218 et al, 2008, vasorelaxant activities (Astulla et al, 2008), antimicrobial and antifungal activities (Darabpour et al, 2011;Sarpeleh et al, 2009;Arshad et al, 2008), hypoglycemic effects (Singh et al, 2008), antidepressant effects (Farzin and Mansouri, 2006), hallucinogenic effects (Glennon et al, 2000), antileishmanial, insecticidal and repellent activities (Mohammad and Mazen, 2009) and promoting wound healing (Derakhshanfar et al, 2010), and were strong inhibitors of monoamine oxidase (Herraiz et al, 2010;Schwarz et al, 2003) and cholinesterase (Zheng et al, 2009(Zheng et al, , 2011Zhao et al, 2013). However, the seeds and aerial parts of P. nigellastrum and P. multisectum were sometimes used as substitutes of P. harmala in medicinal markets, which might result in inconsistencies in the clinical efficacy and therefore create a potential health hazard.…”
Section: Introductionmentioning
confidence: 96%
“…This alkaloid acts on CNS inhibiting the monoamino-oxidase (MAO) (Breakefield et al 1976, Pires et al 2010). Inhibitors of MAO induce an enhancement of the amine concentration in brain, mainly dopamine, noradrenalin and serotonin, generating a state of excitement, euphoria, increased psychomotor activity (antidepressant), and others (Farzin and Mansouri 2006). It is also observed hallucinogenic effect attributed to structural similarity with endogenous amines, such as tryptamine and serotonin (Fortunato 2009).…”
mentioning
confidence: 99%