TABLE 4.
Potential natural products for the treatment of PSD by other mechanisms.
| Studied Drugs | Mechanisms | Description of Study along with Doses | Studied Species | Behavioral Tests | Animal Models | References |
|---|---|---|---|---|---|---|
| Harmane, norharmane and harmine | Inverse-agonistic mechanism located in the benzodiazepine receptors | Treatment of animals with harmane, norharmane and harmine reduced dose-dependently the time of immobility | Male swiss-webst | FST | Acute stress model | Farzin et al., 2006 (Farzin and Mansouri, 2006) |
| Sanguinarine | A decrease in expression of Mkp-1 and increase in ERK activation | A single bilateral intra--the ventrolateral orbital cortex (VLO) infusion of Sanguinarine significantly reduced immobility time in the FST in dose-dependent fashion | Male sprague-da | FST | Acute stress model | Chen et al., 2012 (Chen et al., 2012) |
| β-caryophyllene---β | Action on cannabinoid receptor subtype 2 | Mitigates the stress-related changes in the hippo-campus region | Male swiss mice | TST and FST | Acute stress model | Hwang et al., 2020 (Hwang et al., 2020) |
| Salvinorin A | Mediated by both k-opioid and endocannabinoid systems | Salvinorin A exhibited both anxiolytic- and antidepressant-like effects | Adult male sprague-dawley rats and swiss mice | TST and FST | Acute stress model | Braida et al., 2009 (Braida et al., 2009) |
| Glycyrrhizin | Blocking the activities of HMGB1 | Reduce immobility time of mice in FST and TST model | BABL/c mice | FST and TST | CUMS model | Wang et al., 2018 (Wang et al., 2018) |
| Guarana | Nuclear | Guarana significantly reduced the duration of immobility in the FST suggesting an antidepressant-like effect in mice | Mice | FST | Acute stress model | Campos et al., 2005 (Campos et al., 2005) |
| Hydro-ethanolic of extract Aloysia polystachya (CEAp) | Unclear | A single dose of hydro-ethanolic of extract Aloysia polystachya (CEAp) provoked a significant reduction of the immobility time of male mice in the FST | Swiss albino male | FST | Acute stress model | Lbarrola et al., 2008 (Hellión-Ibarrola et al., 2008) |
| Lafoensia pacari A. St.-Hil. (Lythraceae) | Unclear | The daily treatment for 21 days with ethanolic extract of Lafoensia pacari (PEtExt) increased the latency to immobility and decreased the immobility time, PEtExt 0.1 only decrease the immobility time | Male swiss mice | FST, TST, and OFT | Acute stress model | Galdino et al., 2009 (Galdino et al., 2009) |
| Aqueous root extract of Securidaca longepedunculata (polygalaceae) | With possible involvement of opioidergic pathways | The extract also produced a significant (p < 0.05) naloxone reversible antidepressant like effect in the FST | Swiss albino mice | FST | Acute stress model | Adebiyi et al., 2006 (Adebiyi et al., 2006) |
| D-004 | Unclear | D-004 administered orally for 30 days reduced the immobility in the FST and the TST in mice, and had no effect on other behavioural tests in mice | Adult swiss OF1 | FST and TST | Acute stress model | Garbajal et al., 2009 (Carbajal et al., 2009) |
| Asiaticoside | Unclear | Asiaticoside significantly decreased immobility time in FST and TST, but its mechanism is still unclear and required to be further investigated (Dhingra and Valecha, 2014a) | Male swiss mice | FST, TST, and OFT | CUMS model | Liang et al., 2008 (Liang et al., 2008) |
| Hydroalcoholic extract of Gastrodia elata | Unclear | G. elata aqueous ethanol extract significantly reduced the immobility duration in FST and TST | Male kunming mi | FST, TST and OFT | Acute stress model | Zhou et al., 2006 (Zhou et al., 2006) |
| Hydroethanolic and dichloromethanic extracts Sonchus oleraceus | Unclear | Hydroethanolic and dichloromethanic extracts Sonchus oleraceus reduced the immobility duration in FST and TST, while the mechanism has not been known | Adult male swiss mice | FST and TST | Acute stress model | Vilela et al., 2010 (Vilela et al., 2010) |
| Ethanolic extract of Hypericum perforatum | Unclear | H. perforatum extract displays dose-dependent antidepressant effect | Mice | OFT | Acute stress model | Kumar et al., 2000 (Kumar et al., 2000) |