Phytochemical and pharmacological activities of Solanum surattense Burm. f.–A review

Medicinal plants are unique in having the ability to produce diverse chemical compounds with remarkable biologicalactivities. Investigations of medicinal plants resulted in the discovery of a large number of bioactive compoundswith excellent therapeutic properties. Solanum surattense, a perennial wild growing medicinal herb, is widely usedin the traditional medicine. Exhaustive literature availability reveals the presence of phytochemical compounds fromdifferent plant parts like roots, stem, leaves, fruits, and seeds reported to possess a wide range of pharmacologicalactivities like hepatoprotective, cardioprotective, antiasthmatic and mosquito repellents properties. Intensiveinvestigation on phytochemical constituents resulted in isolation of alkaloid and steroidal compounds solasonoine,solamargine, campesterol, and diosgenin. Evaluation of therapeutic activity of isolated compounds proved as potentones with reference to the standard. Current literature on the pharmacological activity of S. surattense confirms thescientific validation of folklore claims and its traditional use to cure various ailments. Present review is undertaken tosummarize all the available information on pharmacological activities, which provide a baseline support for furtherexploration of its unexplored therapeutic effects like immunomodulation, antipiles activity, antianaphylactic activity,and sexual behavior claimed by folklore.

Phytochemical and pharmacological activities of Solanum surattense Burm. f.–A review

Medicinal plants are unique in having the ability to produce diverse chemical compounds with remarkable biologicalactivities. Investigations of medicinal plants resulted in the discovery of a large number of bioactive compoundswith excellent therapeutic properties. Solanum surattense, a perennial wild growing medicinal herb, is widely usedin the traditional medicine. Exhaustive literature availability reveals the presence of phytochemical compounds fromdifferent plant parts like roots, stem, leaves, fruits, and seeds reported to possess a wide range of pharmacologicalactivities like hepatoprotective, cardioprotective, antiasthmatic and mosquito repellents properties. Intensiveinvestigation on phytochemical constituents resulted in isolation of alkaloid and steroidal compounds solasonoine,solamargine, campesterol, and diosgenin. Evaluation of therapeutic activity of isolated compounds proved as potentones with reference to the standard. Current literature on the pharmacological activity of S. surattense confirms thescientific validation of folklore claims and its traditional use to cure various ailments. Present review is undertaken tosummarize all the available information on pharmacological activities, which provide a baseline support for furtherexploration of its unexplored therapeutic effects like immunomodulation, antipiles activity, antianaphylactic activity,and sexual behavior claimed by folklore.

In vitro activities of glycoalkaloids from the Solanum lycocarpum against Leishmania infantum

ABSTRACT Leishmania infantum is an etiologic agent of visceral leishmaniasis. This disease is a neglected disease that can be fatal if not treated and additionally, the few therapeutic option present several drawbacks, including difficult route of administration and toxicity, which turn the search for new therapeutic alternatives necessary. Herein, we evaluated the leishmanicidal in vitro activity of the solanum extract from Solanum lycocarpum A. St.-Hil., Solanaceae, and the isolated alkaloids solasodine, solamargine and solasonine against promastigotes and intracellular amastigotes of L. infantum. Solasodine (IC50-pro = 4.7 µg/ml; IC50-ama = 10.8 µg/ml) and solamargine (IC50-pro = 8.1 µg/ml; IC50-ama = 3.0 µg/ml) exhibited interesting leishmanicidal ativity. Solasonine was approximately four-times (Selective Index 3.7) more selective to the parasite than to the host cells. This data suggest that solasonine might be considered as a potential drug candidate for leishmaniasis treatment.

In vitro & in vivo estrogenic activity of glycoside fractions of Solanum nigrum fruit.

Background & objectives: The mature fruits of Solanum nigrum contains steroidal glycosides. These are often used as vegetable and there are evidences on tribal use of these fruits as an oral contraceptive. The present study was carried out to evaluate the estrogenic potential of S. nigrum fruits by in vitro and in vivo assays. Methods: Defatted methanol extract of dried S. nigrum fruits was column fractionated and the glycoside positive fractions pooled. Definite concentrations of the fraction were used for in vitro and in vivo assays. The effect on cell viability was analyzed in MCF-7 cell lines by MTT assay followed by in vitro evaluation of estrogenicity by hydroxy apatite (HAP) binding assay. The results were further evaluated in vivo by performing uterotrophic assay in ovariectomized mouse models. Results: At low concentration (40 μg/ml), SNGF induced a dose-dependent increase in MCF-7 cell proliferation, while higher extract concentrations (80-320 μg/ml) caused progressive cell growth inhibition. The competitive binding assay using 3H-E2 suggests that this effect is mediated by estrogen receptor. Mouse uterotrophic assay revealed a classical uterotrophic response in ovariectomized mice in response to S. nigrum glycoside fraction (SNGF). SNGF at a dose of 100 mg/kg of body wt induced the maximum height of luminal epithelial cells which indicated an increase of 30.8 per cent over control (P<0.01) with a correlated increase in uterine wet wt (150% increase over control). Higher doses (250 and 500 mg/kg body wt) of SNGF did not induce any uterotrophic effect. Interpretation & conclusions: Our preliminary data demonstrate the hormone like activity of Solanum glycosides both in vitro and in vivo in mouse, which needs to be further explored to evaluate the possible mechanism and clinical implications.

Role of solasodine hydrochloride in AS2O3 induced HeLa cells apoptosis as well as its effect on cell telomerase activity in vitro / 中国地方病学杂志

Objective To study whether solasodine hydrochloride (SBHL) could enhance the effect of arsenic trioxide in inducing apoptosis and affecting telomerase activity in cervical cancer HeLa cells. Methods Using cell culture methods, cervical cancer HeLa cells were cultured in vitro. The optimal concentration of SBHL was determined by MTT method from 0, 10, 20, 40, 80, 160, to 320 μmol/L. HeLa cells were grown in improved RPMI1640 supplemented respectively with arsenic trioxide(5 μmol/L As2O3), As2O3(5 μmol/L)+ SBHL( 40 μmol/L) and none (control group). The growth morphology of HeLa cells was observed under phase contrast microscopy after culture for 24, 48, and 72 h. Apoptosis of HeLa cells was determined under transmission electronic microscopy. The method of MTT was used to study the cell survival percentage. The technique of flow cytometry was used to measure cell cycle and cell apoptosis percentage. The method of tartrate-resistant acid phosphatase-enzyme linked immunosorbent assay (TRAP-ELISA) was used to determine telomerase activity of HeLa cells. Results Under phase contrast microscopy, in control group HeLa cells were round, densely packed; in As2O3 group the numbers of the cells were less, cell spacing increased; in As2O3 + SBHL group the cells shrinked significantly, nuclear fragmented as a petal-like, gap became larger. Under transmission electronic microscopy, there were rich microvillus on the cell surface in control group, cell intervals clear, immature connections, and the intervals did not close. The structure of the mitochondria in the cytoplasm was integrated. Most of the chromatin in the nucleus were, euchromatin and characteristics of apoptosis with heterochromatin increased and the chromatin condensed into masses, on the boundary of nuclear membrane. The microvillud on the cell surface were ruptured and decreased in As2O3 + SBHL group. The chromatin condensed into masses. The formation of apoptotic bodies was observed. The difference was statistically significant between groups in cell survival percentage at 24, 48, 72h(x2 = 10.39 , 13.88 , 17.21,respectively, all P < 0.05). Cell survival percentage in SBHL + As2O3 group (52.80%) was significantly less than that of As2O3 group(77.51%, x2 = 9.29, P < 0.05) at 72 h. In cell cycles, the difference was statistically significant between groups in C1 phase and S phase(F = 7.46,22.14, all P < 0.05), respectively. Compared with , control group[ (41.57 ± 1.56)%, (50.45 ± 2.37)%], cell percentages in S phase in As2O3 + SBHL group[(20.06 ± 4.98)%] and As2O3 group[(27.10 ± 5.32)%] were decreased(P< 0.05 or < 0.01), while cell percentage in C1 phase was increased[(58.70 ± 5.18)%, (69.67 ± 4.17)%, P< 0.05 or < 0.01]. The difference was statistically significant between groups in apoptotic percentage of HeLa cells (F = 4.01, P < 0.05). Compared with control group[ (1.18 ± 1.40)%], apoptosis percentage was significantly increased in As2O3 + SBHL group and As2O3 group [(21.08± 1.22)%, (6.04±2.53)%, P< 0.05 or < 0.01], respectively, and As2O3 + SBHL group was higher than As2O3 group(P < 0.01). The difference was statistically significant between groups in telomerase activity (F = 21.28, P< 0.05). Telomerase activity was inhibited in As2O3 group(1.214 ± 0.621) and As2O3A + SBHL group(0.865 ± 0.284) compared to control group (2.107 ± 0.057, all P < 0.05), and telomerase activity in As2O3 + SBHL group was lower than that of As2O3 group (P < 0.05). Conclusions SBHL enhances the effect of As2O3 in inducing apoptosis in HeLa cells, which is related to its inhibiting telomerase activity in HeLa cells.

Studies on the alkaloids of Solanum of northeastern Brazil

In our continued studies on the genus Solanum for detecting a good source of soladodine, the steroid alkaloid potentially important for the manufacture of steroid hormones, as well as other compounds of potential therapeutic value, we investigated the fruits of Solanum crinitum, S. rhytidoandrum, and S. jabrense belonging to the subgenus Leptostemonum and S. stipulaceum, belonging to the subgenus Brevantherum, allof which are native of the northeastern region of Brazil and yielded solasodine in moderate to high yield.