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1.
Environ Sci Pollut Res Int ; 31(29): 42277-42294, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38865046

ABSTRACT

Intercropping is a sustainable strategy recognized for boosting crop production and mitigating heavy metal toxicity in contaminated soils. This study investigates the effects of biochar amendments on Pb-contaminated soil, utilizing monocropping and intercropping techniques with C. olitorius and Z. mays. The research assesses Pb removal capacity, nutrient uptake, antioxidant enzymes, and soil Pb fractionation. In monocropping, the phytoremediation ratio for C. olitorius increased from 16.67 to 27.33%, while in intercropping, it rose from 19.00 to 28.33% with biochar amendments. Similarly, Z. mays exhibited an increased phytoremediation ratio from 53.33 to 74.67% in monocropping and from 63.00 to 78.67% in intercropping with biochar amendments. Intercropping significantly increased the peroxidase (POD) activity in Z. mays roots by 22.53%, and there were notable increases in shoot POD of C. olitorius (11.54%) and Z. mays (16.20%) with biochar application. CAT showed consistent improvements, increasing by 37.52% in C. olitorius roots and 74.49% in Z. mays roots with biochar. Biochar amendments significantly increased N content in soil under sole cropping of Z. mays and intercropping systems. In contrast, Cu content increased by 56.34%, 59.05%, and 79.80% in monocropping (C. olitorius and Z. mays) and intercropping systems, respectively. This suggests that biochar enhances nutrient availability, improving phytoremediation efficacy in Pb-contaminated soil. Phyto availability of trace metals (Zn, Mn, Cu, and Fe) exhibited higher levels with biochar amendments than those without. The findings indicate that intercropping and biochar amendments elevate antioxidant enzyme levels, reducing reactive oxygen species and mitigating Pb toxicity effects. This approach improves phytoremediation efficiency and holds promise for soil pollution remediation while enhancing nutrient content and crop quality in Pb-contaminated soil.


Subject(s)
Biodegradation, Environmental , Charcoal , Corchorus , Lead , Soil Pollutants , Soil , Zea mays , Charcoal/chemistry , Soil/chemistry , Metals, Heavy
2.
Toxicol Ind Health ; 37(10): 594-602, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34486900

ABSTRACT

Recently, nanoparticles are emerging as a potential alternative to synthetic pesticides for protection against stored-product insect pests, such as the rice weevil Sitophilus oryzae; however, the toxic effects of nanoparticles on nontarget organisms are not yet understood. Therefore, we investigated the insecticidal effects of synthesized aluminum oxide nanoparticles (Al2O3-NPs) on S. oryzae, as well as their potential toxicity in albino rats. S. oryzae mortality increased as the period of Al2O3-NP exposure increased; 100% mortality was reached at 8000 mg Al2O3-NPs/kg of wheat grain after 7 days of exposure. After 60 days of exposure, all tested Al2O3-NPs concentrations (1000, 2000, 4000, and 8000 mg/kg grain) significantly reduced the number of S. oryzae offspring in a dose-dependent manner. In albino rats, exposure to the LC90 of Al2O3-NPs in a treated diet caused a significant decrease in total body weight and an increase in liver weight in a subacute toxicity test. Moreover, Al2O3-NP treatment elevated the levels of alanine aminotransferase, aspartate aminotransferase, and creatinine in exposed rats relative to control rats, while the uric acid levels of treated rats decreased. Histopathological analysis also revealed various hepatic and renal lesions in treated rats. In summary, although Al2O3-NPs have insecticidal effects, they also have hazardous toxicological effects on rats. Therefore, if Al2O3-NPs are used in the current powder form to protect stored products, they may cause adverse effects to workers and consumers. Further research will be required to develop new nanoformulations with increased safety and potency before these nanoparticles can be used in stored-product pest control.


Subject(s)
Aluminum Oxide/toxicity , Insecticides/toxicity , Metal Nanoparticles/toxicity , Weevils/drug effects , Animals , Dose-Response Relationship, Drug , Liver/pathology , Mortality , Nanoparticles , Rats , Triticum
3.
J Complement Integr Med ; 18(1): 75-86, 2020 May 26.
Article in English | MEDLINE | ID: mdl-32452823

ABSTRACT

OBJECTIVE: The present study aimed to evaluate cytotoxic, apoptotic, and anti-inflammatory properties of bee venom (BV) as well as changes in cytokine secretion levels and nitric oxide (NO) production using three different cancer cell lines [liver (Hep-G2), breast (MCF-7), and cervical (HPV-18 infected HeLa cells)] and two normal cells (splenocytes and macrophages (MQ). METHODS: Cytotoxic activity of BV against tumor cell lines and normal splenocytes/MQ was tested by MTT assay. By ELISA (ELISA); Tumor necrosis factor (TNF-α), Interleukine (IL-10) and interferon (IFN-γ) were measured. Caspase three expressions was evaluated using reverse transcription-polymerase chain reaction (RT-PCR). Nitric oxide (NO) was estimated using a colorimetric assay. RESULTS: BV has a significant cytotoxic effect on all cell lines in a dose- and time-dependent manner; none of them was toxic for normal cells. Treating Hep-G2 cells with BV showed a reduction in IL-10, elevation in TNF-α with no change in IFN-γ level. MCF-7 cells have low IL-10 and TNF-α and high IFN-γ production level. Elevation of IL-10 and IFN-γ coincides with a reduction in TNF-α level was demonstrated in HeLa cells. The expression of Caspase three was dramatically increased with elevation in BV concentration in all tested cancer cell lines. A gradual decrease in NO production by MQ with increasing BV dose was observed. CONCLUSION: Taken together, our results stressed on the importance of BV as a potent anti-tumor agent against various types of cancers (Liver, Breast, and Cervix). Further steps towards the use of BV for pharmacological purposes must be done.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Apoptosis/drug effects , Bee Venoms/pharmacology , Cytokines/drug effects , Inflammation Mediators/metabolism , Caspase 3/drug effects , Cell Line, Tumor , HeLa Cells , Humans
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