In vivo pretreatment of Eudrilus eugeniae powder attenuates β-adrenoceptor toxicity mediated by isoproterenol in rat model

Abstract The present study was designed to discover the potential cardioprotective function of earthworm powder (EWP) extracted from Eudrilus eugeniae on isoproterenol (ISO)-induced myocardial infarction in male Wistar rats. The rats were divided into four groups, with six rats in each group. Certain rats were pretreated with EWP (200 mg/kg bwt) (Group III), and a myocardial infarction was then induced by subcutaneous injection of ISO (85 mg/kg bwt) (Group II). Oral pretreatment of 200 mg/kg bwt of EWP for 28 days significantly (p > 0.05) improved the blood profile levels, including (a) the lipid profile of total cholesterol (TC), free fatty acids (FFA), and triglycerides (TG); (b) low-density lipoprotein (LDL), very low-density lipoprotein (VLDL), high-density lipoprotein (HDL), and protein; and (c) A/G ratio, glucose and uric acid levels. The electrophoretic pattern of elevated lactose dehydrogenase (LDH) levels was recovered by EWP treatment as evidenced by comparison with ISO-induced rats with cardiac damage. The above results indicate that EWP (200 mg/kg bwt) provides a cardioprotective effect by attenuating the blood profile, lipid profile, biochemical levels, and LDH patterns in rats that experienced an ISO-induced myocardial infarction

Design of polymeric materials for culturing human pluripotent stem cells: progress toward feeder-free and xeno-free culturing

This review describes recent developments regarding the use of natural and synthetic polymers to support the propagation of human pluripotent stem cells (hPSCs), human embryonic stem cells (hESCs), and induced pluripotent stem cells (hiPSCs) while maintaining pluripotency in feeder-free and xeno-free cultures. The development of methods for culturing these cells without using mouse embryonic fibroblasts (MEFs) as a feeder layer will enable more reproducible culture conditions and reduce the risk of xenogenic contaminants, thus increasing the potential clinical applications of differentiated hPSCs. Human or recombinant fibronectin, laminin-511, and vitronectin, which are components of the extracellular matrix (ECM), have been used instead of Matrigel for the feeder-free growth of undifferentiated hPSCs. Successful hPSC cultures have been described for the following conditions: on oligopeptide-immobilized surfaces derived from vitronectin, on microcarriers prepared from synthetic polymers, and encapsulated within three-dimensional (3D) hydrogels composed of alginate and other hydrophilic natural polymers. Recently, synthetic biomaterials that allow hPSCs to maintain pluripotency by secreting endogenous ECM components have been designed. The combination of human ECM proteins or cell adhesion molecules (e.g., oligopeptides and poly-d-lysine) and synthetic biomaterials with well-designed surfaces and/or structures (e.g., scaffolds, hydrogels, microcarriers, microcapsules, or microfibers) in the presence of a chemically defined medium containing recombinant growth factors would offer a xeno-free alternative to feeder cells for culturing hPSCs and maintaining their pluripotency

External stimulus-responsive biomaterials designed for the culture and differentiation of ES, iPS, and adult stem cells

The physical and chemical characteristics of biomaterial surface and hydrogels can be altered by external stimuli, such as light irradiation, temperature changes, pH shifts, shear stress forces, electrical forces, and the addition of small chemical molecules. Such external stimulus-responsive biomaterials represent promising candidates that have been developed for the culture and differentiation of embryonic stem (ES) cells, induced pluripotent stem (iPS) cells, and adult stem cells. Biomaterials that are designed to respond in a reversible manner to specific external signals can be formed on micropatterned or non-micropatterned surface, in hydrogels, or on microcarriers. Stem cells and the cells differentiated from them into specific tissue lineages can be cultured and/or differentiated on dishes with immobilized external stimulus-responsive polymers. Cells can be detached from these dishes without using an enzymatic digestion method or a mechanical method when the appropriate external stimulus is generated on the surface. This review discusses the polymers and polymeric designs employed to produce surface and hydrogels for stem cell culture, differentiation, and/or cell detachment using various external stimuli

Flower-like copper sulfide nanocrystals are highly effective against chloroquine-resistant plasmodium falciparum and the malaria vector Anopheles stephensi

Anopheles stephensi is a mosquito of outstanding public health relevance, acting as a major vector of malaria in a number of tropical and subtropical areas worldwide. In recent years, important efforts have been conducted to propose nano-formulated larvicides as valuable alternatives to synthetic insecticides currently marketed. In the present study, the toxicity of flower-like copper sulfide (CuS) nanocrystals has been investigated on the malaria vector A. stephensi and Plasmodium parasites. Characterization of synthesized CuS nanocrystals was carried out using FTIR spectroscopy, XRD analysis, FESEM, HR-TEM and EDS. In mosquitocidal assays, LC50 values ranged from 23.347 ppm (first-instar larvae) to 48.789 ppm (pupae). In vitro anti-plasmodial activity of CuS nanoflowers was evaluated against chloroquine-resistant (CQ-r) and CQ-sensitive (CQ-s) strains of Plasmodium falciparum. IC50were 83.44 μg/mL (CQ-s) and 87.15 μg/mL (CQ-r). However, in vivo antiplasmodial experiments conducted on Plasmodium berghei infecting albino mice showed limited activity of CuS nanocrystals, if compared to CQ. Overall, our findings showed that chemically synthesized flower-like CuS nanocrystals are promising to improve the effectiveness of mosquito control programs, as well as to develop novel antiplasmodial drugs

Morphological and genetical changes of endothelial progenitor cells afterin-vitroconversion into photoreceptors

Background Retinal degeneration is a condition ensued by various ocular disorders such as artery occlusion, diabetic retinopathy, retrolental fibroplasia and retinitis pigmentosa which cause abnormal loss of photoreceptor cells and lead to eventual vision impairment. No efficient treatment has yet been found, however, the use of stem cell therapy such as bone marrow and embryonic stem cells has opened a new treatment modality for retinal degenerative diseases. The major goal of this study is to analyze the potential of endothelial progenitor cells derived from bone marrow to differentiate into retinal neural cells for regenerative medicine purposes. Methods In this study, endothelial progenitor cells were induced in-vitro with photoreceptor growth factor (taurine) for 21 days. Subsequently, the morphology and gene expression of CRX and RHO of the photoreceptors-induced EPCs were examined through immunostaining assay. Findings The results indicated that the induced endothelial progenitor cells demonstrated positive gene expression of CRX and RHO. Our findings suggested that EPC cells may have a high advantage in cell replacement therapy for treating eye disease, in addition to other neural diseases, and may be a suitable cell source in regenerative medicine for eye disorders

Towards bio-encapsulation of chitosan-silver nanocomplex? Impact on malaria mosquito vectors, human breast adenocarcinoma cells (MCF-7) and behavioral traits of non-target fishes

In this study, we synthesized and bio-encapsulated a chitosan-silver nanocomplex (Ch-AgNPs), characterizing it by UV–Vis spectroscopy, FTIR, EDX, SEM, XRD and Zeta potential analyses. The bio-encapsulated chitosan-Ag nanocomplex (BNC) was efficient as scavenger of free radicals (DPPH and ABTS), if compared to Ch-AgNPs. In toxicity assays against breast cancer cells (MCF-7) the BNC triggered apoptotic pathways, leading to a decline of MCF-7 cell viability with IC50 of 17.79 μg/mL after 48 h of exposure. LC50 of BNC on Anopheles stephensi ranged from 54.65 (larva I), to 98.172 ppm (pupa) while Ch-AgNPs LC50 ranged from 4.432 (I) to 7.641 ppm (pupa). In the field, the application of Ch-AgNP (10 × LC50) lead to A. stephensi larval reduction to 86.2, 48.4 and 100% after 24, 48, and 72 h, while the BNC nanocomplex exhibited 68.8, 36.4 and 100% larval reduction, respectively. Both Ch-AgNPs and the BNC reduced longevity and fecundity of A. stephensi. As regards to non-target effects on fish behavioral traits, in standard conditions, Poecilia reticulata predation on A. stephensi larvae was 70.25 (II) and 46.75 larvae per day (III), while post-treatment with sub-lethal doses of BNC, predation was boosted to 88.5 (II) and 70.25 (III) larvae per day

Stem cell therapies for reversing vision loss

Current clinical trials that evaluate human pluripotent stem cell (hPSC)-based therapies predominantly target treating macular degeneration of the eyes because the eye is an isolated tissue that is naturally weakly immunogenic. Here, we discuss current bioengineering approaches and biomaterial usage in combination with stem cell therapy for macular degeneration disease treatment. Retinal pigment epithelium (RPE) differentiated from hPSCs is typically used in most clinical trials for treating patients, whereas bone marrow mononuclear cells (BMNCs) or mesenchymal stem cells (MSCs) are intravitreally transplanted, undifferentiated, into patient eyes. We also discuss reported negative effects of stem cell therapy, such as patients becoming blind following transplantation of adipose-derived stem cells, which are increasingly used by 'stem-cell clinics'

Suaeda maritima-based herbal coils and green nanoparticles as potential biopesticides against the dengue vector Aedes aegypti and the tobacco cutworm Spodoptera litura

The overuse of synthetic pesticides to control insect pests leads to physiological resistance and adverse environmental effects, in addition to high operational cost. Insecticides of botanical origin have been reported as useful for control of agricultural and public health insect pests. This research proposed a novel method of mangrove-mediated synthesis of insecticidal silver nanoparticles (AgNP) using Suaeda maritima, acting as a reducing and stabilizing agent. AgNP were characterized by UV–vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD) analysis. S. maritima aqueous extract and mangrove-synthesized AgNP showed larvicidal and pupicidal toxicity against the dengue vector Aedes aegypti and the tobacco cutworm Spodoptera litura. In particular, LC50 of AgNP ranged from 8.668 (larva I) to 17.975 ppm (pupa) for A. aegypti, and from 20.937 (larva I) to 46.896 ppm (pupa) for S. litura. In the field, the application of S. maritima extract and AgNP (10 × LC50) led to 100% mosquito larval reduction after 72 h. Smoke toxicity experiments conducted on A. aegypti adults showed that S. maritima leaf-, stem- and root-based coils evoked mortality rates comparable or higher if compared to permethrin-based positive control (62%, 52%, 42%, and 50.2 respectively). In ovicidal experiments, egg hatchability was reduced by 100% after treatment with 20 ppm of AgNP and 250 ppm of S. maritima extract. Furthermore, low doses of the AgNP inhibited the growth of Bacillus subtilis, Klebsiella pneumoniae and Salmonella typhi. Overall, our results highlighted the potential of S. maritima-based herbal coils and green nanoparticles as biopesticides in the fight against the dengue vector A. aegypti and the tobacco cutworm S. litura

Continuous harvest of stem cells via partial detachment from thermoresponsive nanobrush surfaces

Stem cell culture is typically based on batch-type culture, which is laborious and expensive. Here, we propose a continuous harvest method for stem cells cultured on thermoresponsive nanobrush surfaces. In this method, stem cells are partially detached from the nanobrush surface by reducing the temperature of the culture medium below the critical solution temperature needed for thermoresponse. The detached stem cells are harvested by exchange into fresh culture medium. Following this, the remaining cells are continuously cultured by expansion in fresh culture medium at 37 °C. Thermoresponsive nanobrush surfaces were prepared by coating block copolymers containing polystyrene (for hydrophobic anchoring onto culture dishes) with three types of polymers: (a) polyacrylic acid with cell-binding oligopeptides, (b) thermoresponsive poly-N-isopropylacrylamide, and (c) hydrophilic poly(ethyleneglycol)methacrylate. The optimal coating durations and compositions for these copolymers to facilitate adequate attachment and detachment of human adipose-derived stem cells (hADSCs) and embryonic stem cells (hESCs) were determined. hADSCs and hESCs were continuously harvested for 5 and 3 cycles, respectively, via the partial detachment of cells from thermoresponsive nanobrush surfaces