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1.
《Saudi Pharmaceutical Journal》2022,30(11):1572-1588
Non-alcoholic fatty liver disease (NAFLD) is one of the most common complications of a metabolic syndrome caused by excessive accumulation of fat in the liver. Orthosiphon stamineus also known as Orthosiphon aristatus is a medicinal plant with possible potential beneficial effects on various metabolic disorders. This study aims to investigate the in vitro inhibitory effects of O. stamineus on hepatic fat accumulation and to further use the computational systems pharmacology approach to identify the pharmacokinetic properties of the bioactive compounds of O. stamineus and to predict their molecular mechanisms against NAFLD. Methods: The effects of an ethanolic extract of O. stamineus leaves on cytotoxicity, fat accumulation and antioxidant activity were assessed using HepG2 cells. The bioactive compounds of O. stamineus were identified using LC/MS and two bioinformatics databases, namely the Traditional Chinese Medicine Integrated Database (TCMID) and the Bioinformatics Analysis Tool for the Molecular Mechanism of Traditional Chinese Medicine (BATMAN-TCM). Pathway enrichment analysis was performed on the predicted targets of the bioactive compounds to provide a systematic overview of the molecular mechanism of action, while molecular docking was used to validate the predicted targets. Results: A total of 27 bioactive compounds corresponding to 50 potential NAFLD-related targets were identified. O. stamineus exerts its anti-NAFLD effects by modulating a variety of cellular processes, including oxidative stress, mitochondrial β-oxidation, inflammatory signalling pathways, insulin signalling, and fatty acid homeostasis pathways. O. stamineus is significantly targeting many oxidative stress regulators, including JNK, mammalian target of rapamycin (mTOR), NFKB1, PPAR, and AKT1. Molecular docking analysis confirmed the expected high affinity for the potential targets, while the in vitro assay indicates the ability of O. stamineus to inhibit hepatic fat accumulation. Conclusion: Using the computational systems pharmacology approach, the potentially beneficial effect of O. stamineus in NAFLD was indicated through the combination of multiple compounds, multiple targets, and multicellular components. 相似文献
2.
This study is focussed on micro-encapsulation of essential oils in polylactic acid (PLA) and a poly(methyl methacrylate) (PMMA) matrix as well as blends of the same. Microspheres were prepared by the solvent evaporation technique and characterised by scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and Fourier transform infra-red spectroscopy (FTIR). The encapsulation efficiencies and release profiles of the essential oils were studied by gas chromatography mass spectrometry (GC-MS) and head-space solid-phase microextraction GC-MS, respectively. Furthermore, the microspheres were tested for antibacterial activity against both Gram-negative and Gram-positive bacterial strains.
The results showed that the microspheres compositions (PLA/PMMA ratio) have significant effect on their characteristics. The process adopted for preparing the microspheres promoted formation of spherical particles at the sizes of 1.5–9.5?µm. The highest encapsulation efficiency of the prepared microspheres was observed in systems consisting of linalool (81.10?±?10.0?wt. % for PLA system and 76.0?±?3.3?wt. % for PMMA system). Confirmation was also made that the release rate of the microspheres was affected by the size of the same. 相似文献
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《Nutrition, metabolism, and cardiovascular diseases : NMCD》2019,29(10):1030-1039
Background and aimThis network meta-analysis (NMA) compares the effects of different types of olive oil (OO) on cardiovascular risk factors.Methods and resultsLiterature search was conducted on three electronic databases (Medline, Web of Science, and Cochrane Central). Inclusion criteria: Randomized controlled trials (RCTs) (≥3 weeks duration of intervention) comparing at least two of the following types of OO: refined OO (ROO), mixed OO (MOO), low phenolic (extra) virgin OO (LP(E)VOO), and high phenolic (extra) virgin OO (HP(E)VOO). Random-effects NMA was performed for seven outcomes; and surface under the cumulative ranking curve (SUCRA) was estimated, using an analytical approach (P-score). Thirteen RCTs (16 reports) with 611 mainly healthy participants (mean age: 26–70 years) were identified. No differences for total cholesterol, HDL-cholesterol, triacylglycerols, and diastolic blood pressure were observed comparing ROO, MOO, LP(E)VOO and HP(E)VOO. HP(E)VOO slightly reduce LDL-cholesterol (LDL-C) compared to LP(E)VOO (mean difference [MD]: −0.14 mmol/L, 95%–CI: −0.28, −0.01). Both, HP(E)VOO and LP(E)VOO reduces SBP compared to ROO (range of MD: −2.99 to −2.87 mmHg), and HP(E)VOO may improve oxidized LDL-cholesterol (oxLDL-C) compared to ROO (standardized MD: −0.68, 95%–CI: −1.31, −0.04). In secondary analyses, EVOO may reduce oxLDL-C compared to ROO, and a dose-response relationship between higher intakes of phenolic compounds from OO and lower SBP and oxLDL-C values was detected. HP(E)VOO was ranked as best treatment for LDL-C (P-score: 0.83), oxLDL-C (0.88), and SBP (0.75).ConclusionsHP(E)VOO may improve some cardiovascular risk factors, however, public health implications are limited by overall low or moderate certainty of evidence. 相似文献
5.
Hamida Hamdi 《Andrologia》2019,51(10)
Sertraline is an antidepressant medication used extensively in the therapy of depression. The present investigation was intended to estimate the actual protective role of wheat germ oil on sertraline‐caused testicular injury in albino rats. Sertraline (human therapeutic dose, 15.63 mg/kg) was orally administrated to rats for 28 successive days. Sertraline‐administered rats were concurrently supplemented with wheat germ oil (human therapeutic dose, 68.75 mg/kg) for 28 successive days. Sertraline administration induced an elevation in testicular DNA damage and acute testicular damage illustrated by the histopathological alterations including marked degeneration and necrosis of germ cells lining seminiferous tubules, as well as interstitial oedema, congestion of interstitial blood vessel. Wheat germ oil administration potentially mitigated the histopathological alterations of sertraline‐administered rats. Lipid peroxidation, oxidative stress biomarker, showed a significant elevation in testicular tissue of sertraline‐administered rats. Furthermore, glutathione content and catalase activity were decreased in testicular tissue of sertraline‐administered rats. Serum testosterone level was elevated in sertraline‐administered rats. Wheat germ oil significantly reduced lipid peroxidation of testicular tissue and improved the antioxidant defences. Finally, wheat germ oil has a preventive role against testicular damage induced by sertraline in rats probably via its potential to prevent reactive oxygen species. 相似文献
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A survey of plants used as wild vegetables was conducted in four districts of Botswana in August and September 2005. The objective was to determine which wild plants were used as vegetables in the study area, and to document their cooking and preservation methods. Fourteen species representing seven families were mentioned as wild vegetables. In addition, six species from four families had other uses in traditional medicine. The implications of the documented processing methods on the retention of nutrients in the vegetables are discussed. 相似文献
8.
棕榈油对成人血脂和血小板功能的影响 总被引:3,自引:0,他引:3
报道了棕榈油(PA),花生油(PE)对血清总胆固醇水平(TC)在5.5~7.0mmol/L的受试者血脂和血小板功能的影响。51名受试者(男31人,女20人,年龄30~66岁之间)分为两组,一组男15人,女11人,称PE组;另一组男16人女9人,称PA组,预备期3周,膳食以当地日常食用的花生油烹调,实验期6周。PA组受试者食用以棕榈油烹调的实验膳;PE组受试者仍食花生油烹调的膳食。脂肪约占膳食能量的30%,其中60%~65%来自实验油。实验结果表明:与起始值相比,6周末PA组受试者血清TC,低密度脂蛋白胆固醇(LDL-C)和总胆固醇与高密度脂蛋白胆固醇比值(TC/HDL-C)显著下降,血浆血栓素B2(TXB2)/6-酮前列环素F1α、(6-keto-PGF1α)比值显著下降,全血血小板聚集率未见显著变化。PE组受试者的血脂、血浆TXB2、6-keto-PGF1α及全血血小板聚集率等指标均未出现显著变化。提示,棕榈油作为我国居民家庭烹调用油并不会增加发生心血管疾病的危险。 相似文献
9.
10.
烹调油烟致大小鼠肺癌的实验研究 总被引:1,自引:0,他引:1
[目的]了解烹调油烟(cooking oil fumes,COF)的动物致癌性。[方法]采用动式染毒法给Balb/c小鼠(雌雄各半)吸入COF浓度为9.09、20.65、38.85mg/m^3,染毒1次/1~2d,30min/次,共150次,计8个月;SD大鼠(雌雄各半)吸入COF浓度为6、88、15.06、35.33mg/m^3,染毒1次/2d,30min/次,共191次,计12.5个月。分别制备COF慢性中毒动物模型;两实验均设空白对照组,吸入与实验组相同温度的清洁空气。[结果]COF诱发Balb/c小鼠实验组肺癌总发生率为18、95%(29/153),低、中、高浓度组肺癌发生率分别为15.09%、20、00%和22.00%,与对照组差异均有显著性。但低、中、高三组间差异无显著性(P〉0.05);COF诱发SD大鼠肺癌总发生率为9、10%(9/99),低、中、高浓度组肺癌发生率分别为6.45%、8.57%、12.12%,高浓度组肺癌发生率高于对照组(P〈0.05)。各性别组间肺癌发生率的差别无显著性(P〉0.05)。[结论]COF可以诱导Balb/c小鼠和SD大鼠肺癌,诱发的肺癌主要为肺腺癌(小鼠28/29,大鼠7/9),余为小细胞肺癌。 相似文献