Bark Extract Research Articles

Use of Guazuma ulmifolia Lam. Stem Bark Extracts to Prevent High-Fat Diet Induced Metabolic Disorders in Mice.

This study aimed to evaluate the effects of supplementation with ethanolic and aqueous extracts from the bark of the stem of Guazuma ulmifolia in mice submitted to a high-fat diet as well as to evaluate the chemical composition of these extracts. The chemical composition and antioxidant potential was evaluated in aqueous and ethanolic extracts of the stem bark. The in vivo test consisted of evaluating the effects of the aqueous and ethanolic extracts of the stem bark on C57BL/6 mice receiving a high-fat diet. The animals were evaluated for weight gain, feed consumption, visceral adiposity, serum, and inflammatory and hormonal parameters. The results of the chemical analyses corroborate those obtained by the literature, which reported gallocatechin, epigallocatechin and epigallocatechin gallate. Compared with the ethanolic extract, the aqueous extract showed greater antioxidant capacity. Both extracts resulted in lower feed consumption in the animals, but they did not influence weight gain or visceral adiposity and resulted in varied changes in the lipid profile. In addition, they did not influence glucose tolerance, insulin sensitivity, or fasting blood glucose. Furthermore, the leptin levels increased, which may have contributed to satiety, but this was shown to have a negative impact on other inflammatory and hormonal parameters. Therefore, under the conditions of this study, the biologically active compounds present in the plant species Guazuma ulmifolia were not able to contribute to the treatment of metabolic changes related to the consumption of a high-fat diet.

Optimization of bioactivities of solvent extracts of bark and heartwood of Pterocarpus marsupium and exploration of neuroprotective effect linking to the major Phytoconstituents

The study aims to evaluate the neuroprotective properties of Pterocarpus marsupium Roxb. The bioactive optimized hydroalcohol-extracted fractions of bark (PMBHA) and heartwood (PMHHA) at 300 and 400 mg/kg were examined in rats with scopolamine-induced neurotoxicity to study oxidative, neurochemical, and neuroinflammation biomarkers. Phenol and flavonoid-rich radical scavengers in contributing total antioxidant capacities of PMBHA and PMHHA quenched peroxyl radicals and protected the cellular membrane and lipoproteins from ROS in DPPH, ORAC, and CAP-e tests. In anticholinesterase activities, PMBHA inhibited AChE (IC50: 54.40 ± 0.98 µg/mL) and BChE (IC50: 50.95 ± 0.98 µg/mL) mixed-competitively, while PMHHA inhibited cholinesterase activities (AChE: 42.23 ± 0.54, and BChE: 47.19 ± 0.65 µg/mL) competitively. Dosage at 300 and 400 mg/kg of PMBHA and PMHHA improved serum and brain oxidative indicators (MDA, SOD, CAT, and GSH), and restored proinflammatory cytokines (TNF-α, and IL-6) leading to enhanced brain cholinesterase and β-secretase levels in neurotoxic rats. GC-MS reported antioxidant, anti-inflammatory, and neuroprotective compounds of PMBHA catechol, thiamet-G, d-Gala-l-ido-octonic amide, falcarinol, D-mannose, ribitol, 1,2,4-cyclopentanetrione, 3-(2-pentenyl)-, hexadecanoic acid methyl ester, n-hexadecanoic acid, oleic acid, and 3,5-Dimethoxybenzyl alcohol, α-epi-7-epi-5-Eudesmol, 1 R,4aR,7 R,8aR)-7-(2-Hydroxypropan-2-yl)-1,4a-dimethyldecahydro naphthalen-1-ol, arctiol, 1,1,4,7-tetramethyldecahydro-1 H-cyclopropa[e]azulene-4,7-diol, 2-Propen-1-ol, 3-(2,6,6-trimethyl-1-cyclohexen-1-yl), 4-t-Butyl-2-[4-nitrophenyl]phenol in PMHHA were responsible in neuroprotection in neurotoxic rats. However, heartwood demonstrated better neuroprotective activities than the bark of P. marsupium due to some of the key compounds (1 R,4aR,7 R,8aR)-7-(2-Hydroxypropan-2-yl)-1,4a-dimethyldecahydronaphthalen-1-ol, 2-Propen-1-ol, 3-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, 4-t-Butyl-2-[4-nitrophenyl]phenol, 1,1,4,7-Tetramethyldecahydro-1 H-cyclopropa[e]azulene-4,7-diol.

Protective effects of <em>Terminalia arjuna</em> bark extracts against glycation induced protein damage, oxidative stress, and hyperpigmentation

Protective effects of <em>Terminalia arjuna</em> bark extracts against glycation induced protein damage, oxidative stress, and hyperpigmentation

Stryphnodendron adstringens bark extracts per solvents different: chemical quantification and antioxidant activity in vitro and in silico

Stryphnodendron adstringens bark extracts per solvents different: chemical quantification and antioxidant activity in vitro and in silico

"Investigation of the Biochemical Effect of Aqueous Extract of Dialium guineense Stem Bark on Haematological Parameters in Rats"

"Investigation of the Biochemical Effect of Aqueous Extract of Dialium guineense Stem Bark on Haematological Parameters in Rats"

Pycnogenol-Assisted Alleviation of Titanium Dioxide Nanoparticle-Induced Lung Inflammation via Thioredoxin-Interacting Protein Downregulation.

Titanium dioxide nanoparticles (TiO2NPs) are used in products that are applied to the human body, such as cosmetics and food, but their biocompatibility remains controversial. Pycnogenol (PYC), a natural extract of pine bark, exerts anti-inflammatory and antioxidant effects. In this study, we investigated whether PYC effectively alleviates pulmonary toxicity induced by airway exposure to TiO2NPs, and the beneficial effects of PYC were explained through the analysis of changes to the mechanism of cytotoxicity. TiO2NPs induced pulmonary inflammation and mucus production, increased the levels of malondialdehyde, and upregulated thioredoxin-interacting protein (TXNIP) and cleaved-caspase 3 (Cas3) in the lungs of mice. However, PYC treatment reduced the levels of all toxicity markers of TiO2NPs and restored glutathione levels. These antioxidant and anti-inflammatory effects of PYC were also demonstrated in TiO2NP-exposed human airway epithelial cells by increasing the mRNA levels of antioxidant enzymes and decreasing the expression of TXNIP, cleaved-Cas3, and inflammatory mediators. Taken together, our results showed that PYC attenuated TiO2NP-induced lung injury via TXNIP downregulation. Therefore, our results suggest the potential of PYC as an effective anti-inflammatory and antioxidant agent against TiO2NP-induced pulmonary toxicity.

Phytochemical Screening, Acute Toxicity and Antibacterial Activity of Methanolic Stem Bark Extract of Hibiscus Rosa-Sinensis

Phytochemical Screening, Acute Toxicity and Antibacterial Activity of Methanolic Stem Bark Extract of Hibiscus Rosa-Sinensis

Microstructure of the dentate gyrus and spontaneous alternation behaviour of male Wistar rats following Rauvolfia vomitoria and Gongronema latifolium extracts administration

Rauvolfia vomitoria (RV) and Gongronema latifolium (GL) are medicinal plants used for the local treatment of various health issues. Their activities on the brain motivated this investigation on the histology and immunohistochemistry of the dentate gyrus and spontaneous alternation behaviour (SAB) of adult Wistar rats following RV root bark and GL leaf extract administrations. Twenty young adult Wistar rats (130–160 g) were assigned into four groups: Group 1 served as the control (5 mL/kg of distilled water placebo), while the test groups 2–4 were, respectively, singly administered 200 of mg/kg of RV, 200 of mg/kg of GL, and their combination. The administrations were oral and lasted for seven days. A T-maze SAB test was carried out, and the animals were sacrificed immediately after ketamine hydrochloride intraperitoneal anaesthesia. Serial sections of the hippocampal region from perfused rat brains were stained with Cresyl fast violet and immunolabelled with neuronal nuclei (NeuN) for neurons and glial fibrillary acidic protein (GFAP) for astrocytes. Results indicated that SAB was significantly (p < 0.05) lower in the test groups. Histologically, Nissl was less distributed in the RV and GL-only groups but not in the combined group, while there was less NeuN positivity in the RV group, with the GL and RV + GL groups not affected. There was less positive GFAP expression in individual RV and GL groups, but not in the RV + GL combined group, all compared with the control. In conclusion, the combination of RV and GL did not improve SAB but modulated Nissl, NeuN, and GFAP expression in the dentate gyrus.

Evaluation of Antioxidant Potential, Enzyme Inhibition, and Chemical Profiling Through Mass Spectrometry on Bark Extract of Berberis aristata

Berberis aristata, a plant from the Berberidaceae family, is renowned for its medicinal properties. The presence of bioactive metabolites in its bark underscores its importance in traditional medicine and pharmacology. This study primarily focuses on the biological activities of the plant bark extract, specifically its antioxidant properties and alpha-glucosidase inhibition. In addition to these activities, mass spectrometry-based compound annotation was conducted to explore the metabolites present in the plant bark extract. In this study, the bark samples were collected and extracted using the cold percolation method with methanol. Subsequently, an ethyl acetate fraction was obtained from the methanol extract using a separating funnel. The methanol extract of the bark showed a total phenolic content (TPC) of 70.056 ± 2.52 mg GAE/g and a total flavonoid content (TFC) of 11.89 ± 0.16 mg QE/g. To determine the antioxidant activity of the samples, a DPPH assay was used. The ethyl acetate fraction of the bark showed potent antioxidant activity with an IC50 value of 188.93 ± 8.35 μg/mL, while the methanol extract of the bark showed radical scavenging activity with an IC50 value of 242.89 ± 4.62 μg/mL. In terms of alpha-glucosidase inhibition, the methanol extract of the bark had low enzyme inhibition activity, but the ethyl acetate fraction exhibited potential inhibition with an IC50 value of 112.99 ± 10.28 µg/mL. These results indicate that the plant bark extract is rich in phenolic content compared to flavonoid content. Additionally, the ethyl acetate fraction of the plant bark exhibits potent radical scavenging activity and inhibition of the digestive enzyme alpha-glucosidase. Mass spectrometric-based identification of metabolites revealed that the methanol extract of the bark contains compounds such as Palmatin, columbamine, and berberal. The presence of these metabolites further supports the medicinal use of this plant bark. These findings enhance the plant's potential in the drug discovery process in the future.

<i>In Vitro</i> Evaluation of Cytotoxicity Induced by Indoxacarb and its Amelioration with <i>Cassia fistula</i> Bark Extract

<i>In Vitro</i> Evaluation of Cytotoxicity Induced by Indoxacarb and its Amelioration with <i>Cassia fistula</i> Bark Extract

Antioxidant Activity Test of Outstreched Bark Extract (Campnosperma Brevipetiolatum Volkens) using the DPPH Method

Outstretched bark (Campnosperma brevipetiolatum Volken) is rich in tannins, flavonoids, alkaloids, and saponins. Herbal plants contain flavonoids, which are excellent antioxidants. Determine the amounts of phytochemical substances present in the sample and assess the antioxidant activity using the DPPH (1.1-diphenyl, 2-picrylhydrazil) technique at concentrations of 50, 100, 150, 200, 250, and 300 parts per million. The presenance of alkaloids alkaloids, saponins, and tannins was detected in the phytochemical screening findings against ethanol extracts of outstretched bark. 96% ethanol solvent is used in the maceration technique of extraction. Vitamin C is the positive control utilized. According to the findings of tests for antioxidant activity, ethanol extract at 11.25 ppm has a very high potential for antioxidant activity because its IC50 value is 3.55 ppm.

Incorporation of Nano-Zinc Oxide as a Strategy to Improve the Barrier Properties of Biopolymer-Suberinic Acid Residues Films: A Preliminary Study.

Finishing coatings in the wood-based composites industry not only influence the final appearance of the product but also serve to protect against fungi and molds and reduce the release of harmful substances, particularly formaldehyde and volatile organic compounds (VOCs). Carbon-rich materials, such as those derived from birch bark extraction, specifically suberin acids, can fulfill this role. Previous research has demonstrated that adding suberin acid residues (SAR) at 20% and 50% by weight significantly enhances the gas barrier properties of surface-finishing materials based on poly(lactide) (PLA) and polycaprolactone (PCL), particularly in terms of total VOC (TVOC) and formaldehyde emissions. This study aims to explore whether these properties can be further improved through the incorporation of nano-zinc oxide (nano-ZnO). Previous research has shown that these nanoparticles possess strong resistance to biological factors and can positively affect the characteristics of nanofilms applied as surface protection. The study employed PLA and PCL finishing layers blended with SAR powder at 10% w/w and included 2% and 4% nano-zinc oxide nanoparticles. The resulting blends were milled to create a powder, which was subsequently pressed into 1 mm-thick films. These films were then applied to raw particleboard surfaces. TVOC and formaldehyde emission tests were conducted. Additionally, the fungal resistance of the coated surfaces was assessed. The results showed that PLA/SAR and PCL/SAR composites with the addition of nano-zinc oxide nanoparticles exhibited significantly improved barrier properties, offering a promising avenue for developing biodegradable, formaldehyde-free coatings with enhanced features in the furniture industry. Furthermore, by utilizing SAR as a post-extraction residue, this project aligns perfectly with the concept of upcycling.

The therapeutic effects of Juglans regia Linn (Walnut) extracts on oral Candida infection

The difficulties associated with oral Candida infection management necessitate the development of novel antifungal medicines in order to widen the spectrum of activity against Candida albicans. The aim of this work is to study the oral anticandidal activity of Juglans regia L. cultivated in Algeria. This plant was chosen due to its traditional use for the treatment of oral infections. Methanolic, ethanolic, butanolic, ethylic acetate and acetonic extracts of the bark of J. regia L. were extracted in a Soxhlet device and screened for in vitro activity against C. albicans. Plant preparations were screened for antifungal activity using a standard agar well diffusion assay. Following a study of the antimicrobial activity of plant extracts, their minimal inhibitory concentration (MIC) and minimal fungicidal concentration (MFC) values were determined using a broth microdilution assay. Among J. regia L. extracts, ethylic acetate extract had potent antifungal activity against Candida strain with diameters of inhibition ranging from 15.16±0.76 to 20.83±0.76 mm, followed by acetonic extract with diameters of inhibition ranging from 14.83±0.76 to 19.33±0.28 mm. The J. regia L. demonstrated MIC values ranging from 0.46875 to 3.75 mg mL-1 and the lowest MIC was recorded for ethylic acetate, acetonic extracts and AMB at 0.46875 mg mL-1. The ethylic acetate extract showed the lowest MFC value (0.9375 mg mL-1), followed by butanolic extract (3.125 mg mL-1). These results indicate that J. regia L. bark extracts can contain compounds with therapeutic potential against oral C. albicans and, hence, their possible use as therapeutic agents for oral candidiasis.

Assessment of Time and Dose-Dependent Killing Assay of Azadirachta Indica Bark Extract and Solanum Xanthocarpum Seed Extract Developed ZNO NPS against Dental Pathogens

Assessment of Time and Dose-Dependent Killing Assay of Azadirachta Indica Bark Extract and Solanum Xanthocarpum Seed Extract Developed ZNO NPS against Dental Pathogens

Evaluation of Antimicrobial Activity and Phytoconstituents of Stem Bark Extract and Vacuum Liquid Chromatographic Fractions of Spondias mombin (Linn)

Evaluation of Antimicrobial Activity and Phytoconstituents of Stem Bark Extract and Vacuum Liquid Chromatographic Fractions of Spondias mombin (Linn)

Evaluation of Haemostatic Potential and HPTLC Fingerprinting of Annona squamosa Linn. Bark Extract

Objectives: The present work focuses on exploring and evaluating the hemostatic property of Annona squamosa Linn. bark. Being a renewable resource, it has the potential to contribute to the hemostatic agent. Hemostatic efficacy of the cold and hot bark extract at different concentrations of 10, 50, 100 & 250 mg/ml of saline were evaluated using whole blood clotting, platelet aggregation test, prothrombin time CAMAG HPTLC system. The hemostatic efficacy. At 250 mg/ml saline, both the extracts showed excellent hemostatic efficacy by clotting blood in 1.2 s and 3 s, respectively. The prothrombin time of cold and hot were 5 s and 5.1 s which were less than that of Liquiplastin partial prothrombin time which was Liquicelin E (13.85 s). Annona squamosa Linn. to be used as a topical hemostatic agent. Saponins, which are known to be antihemorrhagic, were detected by HPTLC. hemostatic efficacy of Annona squamosa Linn. bark was evaluated, which can contribute to the development of a fast-acting, cost-effective, easy-to-use, and sustainable topical hemostat. Keywords: Annona squamosa Linn, Hemostatic activity, Prothrombin time, Activated partial thromboplastin time, HPTLC fingerprint

Evaluation of the Combination Effects of Extracts of Jatropha tanjorensis and Adansonia digitata on Clinical Fungal Isolates

Introduction: The proliferation of fake drugs and the multiple resistance seen in conventional fungicidal drugs has led to the use of medicinal plants to treat fungal infections. There are claims that Jatropha tanjorensis and Adansonia digitata have fungicidal potentials, hence this study. Aim: To evaluate the combination effects of the extracts of Jatropha tanjorensis and Adansonia digitata on clinical fungal isolates. Study Design: Randomized sampling of the plants was done by harvesting the plants from different farm in Nsukka Enugu State. Place and Duration of Study: This study was conducted in Enugu State, South East of Nigeria, from November 2023 to March 2024. Methodology: Phytochemical screening was done on the two plants. The methanolic and aqueous (cold and hot) extracts of these plants bark and stem were assessed for their antifungal activities against six fungal isolates using agar diffusion method. The minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) were done according to standard methods. Results: The plants contain alkaloids, terpenoids, saponins, flavonoids, tannin, glycoside and phenol. The hot water extracts of J. tanjorensis stem gave higher zones of inhibition diameter (IZD) than the methanolic extracts and the methanolic extracts of A. digitata bark gave higher IZD than the aqueous extracts. The combination of these two potent extracts showed greatest inhibition on Aspergillus niger, Candida albican and then least inhibition on Trichophyton shoenleinii, this was found to be statistically significant at (P<.05), the P value was (P=0.001). The lowest (MIC) and (MFC) were recorded in A. niger and Candida albican at (1.5625mg/ml) while the highest (MIC) and (MFC) were recorded in T. shoenleinii, at (25mg/ml). Conclusion: This study revealed that the combined plant extracts were more effective against opportunistic fungi than the dermatophytes.

Phytochemical Study, Antioxidant Activity and GC-MS Analysis of Soymida febrifuga A. Juss

Objectives: To determine antioxidant activity and identify bioactive compounds present in n-Hexane & Ethyl acetate extracts of stem bark of Soymida febrifuga A. Juss. Methods: In the present study stem bark of Soymida febrifuga A. Juss was powdered and subjected to Soxhlet extraction using n-Hexane and Ethyl acetate as solvents. Extracts were analysed for the presence of phytochemicals and antioxidant activity. The Bio-active compounds were identified by Gas chromatography-mass spectrometry. Findings: The qualitative analysis revealed presence of various phytochemicals. GC-MS analysis confirmed the presence of total 28 Medicinally active compounds which included Tetradecane, Hentriacontane, Octacosane, Docosane and Eicosane in n-Hexane extract. 15 Medicinally active compounds were found in ethyl acetate extract which included Purolan, 1,2-Dipropenyl cyclobutane, Hentricontane, 2,6,7-Trimethyl decane, Tetrahydrofurfuryl propionate and Decyl propanoate. Novelty: Though the phytochemical analysis of Soymida febrifuga have been performed by some research groups but there are no reports on identification of Bio-active compounds by GC-MS. The results obtained from present study confirms presence of many compounds of biological significance that warrants further biological and pharmacological study of Soymida febrifuga A. Juss as a potential herbal drug. Keywords: Soymida febrifuga; GC-MS analysis; DPPH assay; n-Hexane; Ethyl acetate

Pre-clinical evaluation of neuroprotective effect of Albizzia lebbeck bark extract in Cuprizone induced Multiple sclerosis

Multiple sclerosis (MS) is a complex and debilitating autoimmune disease of the central nervous system (CNS), affecting millions of individuals worldwide. Despite significant advances in the understanding of its pathogenesis, an effective cure for MS remains elusive. Current treatments are often associated with adverse side effects and limited long-term efficacy. Therefore, there is a growing need for novel therapeutic strategies that can offer both neuroprotection and remyelination. Herbal medicine has emerged as a promising avenue in this regard, with various natural extracts showing potential in preclinical MS models. Among these, Albizia lebbeck bark extract has garnered attention due to its reputed anti-inflammatory and neuroprotective properties. In this research study, we explore the preclinical evaluation of Albizia lebbeck bark extract in cuprizone-induced MS, aiming to shed light on its therapeutic potential and possible mechanisms of action.

Anti-Inflammatory Potential of Pygeum africanum Bark Extract: An In Vitro Study of Cytokine Release by Lipopolysaccharide-Stimulated Human Peripheral Blood Mononuclear Cells.

Pygeum africanum bark has been shown to inhibit the production of pro-inflammatory prostaglandins in the prostate and reduces the production of leukotrienes and other 5-lipoxygenase (5-LO) metabolites. It has been suggested that inflammation plays an important role in the pathophysiology of benign prostatic hyperplasia (BPH). Data from clinical trials have shown that P. africanum improves the symptoms and objective measures of BPH. This in vitro study aimed to assess the anti-inflammatory potential of a proprietary Pygeum bark standardized extract (Prunera®) on cytokine release from lipopolysaccharide-stimulated human peripheral blood mononuclear cells (PBMCs). PBMCs were obtained from four donors, and a bead-based assay (ProcartaPlex™ panel) was used for the detection and quantitation of cytokines. Pygeum africanum bark standardized extract (PABE) induced a statistically significant decrease (p < 0.05) of IL-6 in three donors. Other effects were as follows: IL-2 was lowered in all donors in the absence of a clear dose-response relationship; IL-4, IL-5, IL-9, and IL-13 levels were decreased in most donors; IL-22 levels seemed to be suppressed only for donor 4 at lower and medium concentrations; and IL-27 and TNF-α levels decreased at all PABE concentrations in all donors. The anti-inflammatory effect of PABE, particularly the reduction in IL-6 as a marker of inflammation, supports the potential use of this natural compound in the management of BPH and other conditions in which pro-inflammatory cytokines are involved in their underlying pathophysiological mechanisms.