Summary and Conclusions The preliminary phytochemical analysis reveals that the hydroalcoholic extract of Argyreia nervosa showed positive results towards Alkaloids, tannins, phenolic compounds, Flavonoids, sterols, lignans, sugars; Jasminum sambac showed positive results towards tannins, phenolic compounds, Flavonoids, triterpenoids, sugars, coumarins; Passiflora foetida showed positive results towards alkaloids, tannins, glycosides, phenolics, Flavonoids, sterols, sugars, lignans; Sapindus emarginatus showed positive results towards tannins, phenols, glycosides, sterols, triterpenoids, saponins, sugars, lignans, which was confirmed by TLC and HPTLC studies. The phytoconstituents were isolated by column chromatography and structure was elucidated by spectral studies. Fractionation of extract lead to the isolation and identification of compounds AN-1 and 2 is from AN revealed the phytochemicals as ergometrine and isoquercetin respectively. Chlorocoumarin and Kaempferol as JS-1 and JS-2 from JS. Harmaline and Vertexin as PF-1 and PF-2 from PF. Oleanolic acid and Amyrin respectively as SE-1 and SE-2 from SE. The hydroalcoholic extracts of AN, JS, PF and SE were standardized and the total phenolic contents were found to be 10.58 ± 0.03, 20.64 ± 0.15, 61.63 ± 0.03 and 25.46 ± 0.87 mg GAE/g extract respectively. The total tannic contents were found to be 63.08 ± 1.23, 16.08 ± 1.57, 16.11 ± 0.96 and 71.42 ± 0.24 mg TAE/g extract respectively. The total flavonoid contents were found to be 10.98 ± 0.04, 11.88 ± 0.17 and 11.60 ± 0.23 mg QE/g extract respectively, as SE did not show any response to Flavonoids. Argyreia nervosa, Jasminum sambac, Passiflora foetida and Sapindus emarginatus were found to have potent antioxidant activity, as evident from invitro antioxidant studies against DPPH radical scavenging, Nitric oxide radical scavenging, Hydrogen Institute of Pharmceutical Technology, SPMVV, Tirupati 216 Summary and Conclusions peroxide radical scavenging activities, Reducing power assay, Total antioxidant capacity indicating that AN, JS, PF and SE were effective in scavenging the ROS generated during major depressive disorder. The acute toxicity studies were conducted as per the OECD guidelines 420, where the limit test dose of 2000 mg/kg used. No test substance- related mortality was observed at 2000 mg/kg. The alcoholic extract of AN, JS, PF and SE at a dose of 250 and 500mg/kg orally daily for 28 days did not produce any sign of observable toxicity during the experimental period. All the tested haematological parameters such as Hb, RBC, WBC, PCV; Liver function parameters like AST, ALP, ALT; Kidney function parameters like urea, blood urea nitrogen, creatinine; metabolic indices like LDL, HDL, VLDL, TG, Glucose and Liver, Heart, Lung, Spleen, Kidney and Body Weights were within the normal. No significant change is observed as and when compared to control animals indicating that the plants are safe. In conclusion, this study presents strong evidence of the nontoxic effect of the hydroalcoholic extracts of AN, JS, PF and SE. These results support the use of extract of AN, JS, PF and SE is safe and explained the extensive utilization of the plant in traditional medicine. AN, JS, PF and SE showed no mortality at a dose 2gm/kg indicating its LD50 as 5gm/kg. AN, JS, PF and SE showed decreased immobility in FST and TST indicating their antidepressant activity. AN and SE showed the involvement of serotonergic system in their antidepressant activity, where as PF and JS showed the involvement of adrenergic system. Institute of Pharmceutical Technology, SPMVV, Tirupati 217 Summary and Conclusions The hydroalcoholic extracts of AN, JS, PF and SE were found to be effective against stress induced alterations in Lipid peroxidation, reduced glutathione and vitamin C levels indicating its antioxidant capacity. Further studies are required to evaluate the specific phytoconstituents in AN, JS, PF and SE responsible for antidepressant like activity in order to develop “new lead molecule” as novel therapeutic agent for depression. Institute of Pharmceutical Technology, SPMVV, Tirupati 218
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