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Finding healing power in plants is an ancient idea, and people of all continents and civilization have been using plants in one form or the other for poultices or as decoctions. Alangium salvifolium (Linn), family Alangeaceae, is a tree that grows in the wild throughout India. The plant has been used in the Indian traditional system of medicine for skin diseases (e.g. leucoderma), articular diseases, and anti-inflammation, anti-poisonous, anti-pyretic, and anti-emetic requirements. However, no scientific evidence is available regarding its antimicrobial activity. An investigation of Alangium salvifolium as an antimicrobial activity agent is the objective of our present study. The ATCC culture used in this study was collected from department of Microbiology, G.M.C., Bhopal (M.P.). Shade dried crude powder (200 grams) of seed of Alangium salvifolium was separately extracted with methanol in a soxhelt apparatus. The Antimicrobial activities were then studied by applying the Disc–Diffusion method. Our results indicate that the observed antimicrobial activity of the fraction appears to be due to unknown secondary metabolites in it. H.P.L.C. (high performance liquid chromatography) and chemical studies may, thus be useful in analyzing the presence of unknown secondary metabolites in the fractions.
Salinity stress affects many metabolic facets of plants and induces anatomical and morphological changes resulting in reduced growth and productivity. To overcome the damaging effects of salinity, different strategies of the application of nutrients with plant hormones are being adopted. The present study was carried out with an aim to find out whether application of calcium chloride (CaCl₂) and gibberellic acid (GA₃) could alleviate the detrimental effects of salinity stress on plant metabolism. Fifteen days old plants were supplied with (1) 0 mM NaCl + 0 mg CaCl₂ kg⁻¹ sand + 0 M GA₃ (control, T0); (2) 0 mM NaCl + 10 mg CaCl₂ kg⁻¹ sand + 0 M GA₃ (T1); (3) 0 mM NaCl + 0 mg CaCl₂ kg⁻¹ sand + 10⁻⁶ M GA₃ (T2); (4) 150 mM NaCl + 0 mg CaCl₂ kg⁻¹ sand + 0 M GA₃ (T3); (5) 150 mM NaCl + 10 mg CaCl₂ kg⁻¹ sand + 0 M GA₃ (T4); (6) 150 mM NaCl + 0 mg CaCl₂ kg⁻¹ sand + 10⁻⁶ M GA₃ (T5); (7) 150 mM NaCl + 10 mg CaCl₂ kg⁻¹ sand + 10⁻⁶ M GA₃ (T6). To assess the response of the crop to NaCl, CaCl₂ and GA₃, plants were uprooted randomly at 60 days after sowing. The presence of NaCl in the growth medium decreased all the growth and physio-biochemical parameters, except electrolyte leakage, proline (Pro) and glycine betaine (GB) content, thiobarbituric acid reactive substances (TBARS), H₂O₂ content, activities of superoxide dismutase (SOD) and catalase (CAT) and leaf Na content, which exhibited an increase of 37.6, 29.3, 366.9, 107.5, 59.1, 17.1, 28.4 and 255.2%, respectively, compared to the control plants. However, application of CaCl₂ in combination with GA₃ appears to confer greater osmoprotection by the additive role with NaCl in Pro and GB accumulation. Although the activities of antioxidant enzymes (SOD, CAT and POX) were increased by salt stress, the combined application of CaCl₂ and GA₃ to salt-stressed plants further enhanced the activities of these enzymes by 25.1, 6.7 and 47.8%, respectively, compared to plants grown with NaCl alone. The present study showed that application of CaCl₂ and GA₃ alone as well as in combination mitigated the adverse effect of salinity, but combined application of these treatments proved more effective in alleviating the adverse effects of NaCl stress.
This study was conducted to evaluate the possible protective effects of the flavonoid-rich fraction of Aloe barbadensis leaf skin on cadmium (Cd)-induced toxicity in male albino rabbits. Cadmium is a notable environmental pollutant due to its wider range of toxic manifestations. The aqueous fraction of aloe extract (AAF) showed higher phenolics, flavonoids, and antioxidant capacity among other fractions, suggesting its rationale use in this study. Twenty-four rabbits were randomly divided into four groups, including the control group (receiving only vehicle), the Cd group (receiving Cd, 5.1 mg/kg/day), the AAF groups (receiving AAF, 200 mg/Kg/day), and the Cd+AAF group (receiving the same concentrations as the Cd and AAF groups). Oral treatment over a period of 40 days significantly increased (p<0.05) biochemical marker enzymes, including transaminases (AST, ALT), alkaline phosphatase, γ-glutamyl transferase, creatinine, and urea, while total bilirubin (Tb) and albumin were decreased on days 10, 20, 30, and 40 in the Cd group as compared to control. A significant decrease (p<0.05) in enzyme levels and increases in Tb and albumin for Cd+AAF were observed as compared to Cd-treated rabbits. Contents of superoxide dismutase, catalase, and vitamins C and E in liver and kidney tissues were significantly increased (p<0.05), while cadmium content was significantly decreased (p<0.05) for Cd+AAF rabbits as compared to Cd-intoxicated rabbits. Values of all the parameters in only the AAF group were near to control. The histopathological studies for liver and kidney have also supported the Cd+AAF group markedly reducing the toxicity of Cd in both tissues to near normal. Thus, the results suggest that the flavonoid-rich fraction of AAF may act as a natural protective agent against Cd toxicity via suppressing oxidative stress due to higher antioxidant activity.
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