Table 2.
In vivo studies in the pharmacological evaluation of Pelargonium sidoides DC.
| Biological activity | Extract/formulation | Experimental organism | Test organism | Administration | Dose range | Active concentration | Response | Control | Reference |
|---|---|---|---|---|---|---|---|---|---|
| Antiviral activity | EPs® 7630 | Female BALB/c mice | A/Puerto Rico/8/34H1N1 virus | Inhalation | 5 mg/kg | 5 mg/kg | Increased survival of virus-infected mice | Mice treated with vehicle | Theisen and Muller (2012) |
| Anticoagulant activity | EPs® 7630 | Male Sprague–Dawley rats | N/A | Oral | 10, 75, 500 mg/kg | 500 mg/kg p.o. | No effect on blood coagulation | Warfarin (0.05 mg/kg p.o.) | Koch and Biber (2007) |
| Central nervous system activity | Epigallo- and gallocatechin based oligomers of EPs® 7630 | Male NMRI mice | N/A | – | 200 mg/kg | 200 mg/kg | None to moderate effect on behavioural activity | Mice treated with vehicle | Schötz and Nöldner (2007) |
| Lipopolysaccharide (LPS) induced sickness behaviour | EPs® 7630 | Male NMRI-mice | N/A | Oral | 100, 200, 400 mg/kg | 400 mg/kg | Complete counteraction of LPS-induced sickness-behaviour | Mice treated with vehicle | Nöldner and Schötz (2007) |
EMCV=encephalomyocarditis virus; LPS=lipopolysaccarides; N/A=not applicable; NO=nitric oxide; Warfarin=3-(a-acetonylbenzyl)-4-hydroxy-coumarin.