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1.
Nanomaterials (Basel) ; 14(11)2024 May 29.
Article in English | MEDLINE | ID: mdl-38869577

ABSTRACT

Insulin-loaded nanofibers were prepared using chitosan as a natural polymer. The loaded insulin with polyethylene oxide was used for preparing monolayer batch S1. Nanofiber S1 was coated by seven layers of film on both sides to form batch S2 as a sandwich containing Layer A (CS, PEG and PEO) and Layer B (PEG and PEO) using electrospinning apparatus. SEM, TEM and FT-IR techniques were used to confirm the drug loading within the composite nanofibers. The in vitro activity that provided a sustained and controlled release of the drug from the nanofiber batch was studied at different pH values spectrophotometrically using a dialysis method. In batches S1 and S2, the release of insulin from nanofiber proceeds via burst release necessary to produce the desired therapeutic activity, followed by slow step. The rate and the percentage release of insulin in batch S2 are found to be higher at all pH values.

2.
Physiother Res Int ; 29(3): e2100, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38821882

ABSTRACT

BACKGROUND: Age-related thoracic kyphosis can impair posture, diaphragmatic excursion, respiratory function, and overall quality of life (QoL). PURPOSE: This randomized controlled trial aimed to compare the effects of corrective exercises alone versus combined with diaphragmatic breathing exercises on thoracic kyphosis, diaphragmatic excursion, thoracic pain, and QoL in postmenopausal kyphotic women. METHODS: Forty postmenopausal women diagnosed with thoracic kyphosis were randomly divided into two groups. Group A received corrective exercises for 12 weeks (n = 20), while Group B received both diaphragmatic breathing exercises and corrective exercises for the same duration (n = 20). Primary outcome measures were thoracic kyphosis angle and diaphragmatic excursion, while secondary outcome measures were thoracic pain and QoL. Both groups were assessed pre- and post-intervention using a flexible curve ruler for the thoracic kyphosis angle, ultrasonography for the diaphragmatic excursion, the visual analog scale for thoracic pain, and the Arabic version of the QoL Questionnaire of the European Foundation for Osteoporosis for QoL. RESULTS: Both groups showed significant within-group improvements in all measures post-intervention (p < 0.05). Between-group comparisons post-intervention revealed no significant differences (p > 0.05) except for diaphragmatic excursion, where Group B showed significantly greater improvement (p < 0.05). CONCLUSIONS: A 12-week program of corrective exercises alone or combined with diaphragmatic breathing exercises significantly improved kyphosis angle, thoracic pain, and QoL in postmenopausal kyphotic women. The addition of diaphragmatic breathing exercises provided further benefits by increasing diaphragmatic excursion to a greater degree compared with corrective exercises alone.


Subject(s)
Breathing Exercises , Diaphragm , Kyphosis , Postmenopause , Quality of Life , Humans , Female , Kyphosis/rehabilitation , Kyphosis/diagnostic imaging , Middle Aged , Postmenopause/physiology , Diaphragm/diagnostic imaging , Diaphragm/physiopathology , Aged , Exercise Therapy/methods , Thoracic Vertebrae/diagnostic imaging , Treatment Outcome
3.
Sci Rep ; 14(1): 12583, 2024 05 31.
Article in English | MEDLINE | ID: mdl-38821973

ABSTRACT

This study investigated the effects of dietary supplementation with the product Hilyses on growth performance, feed utilization, nutrient composition, hematological parameters, serum biochemistry, immune function, antioxidant status, and digestive enzyme activity in juvenile Nile tilapia (Oreochromis niloticus, initial body weight 4.24 ± 0.01 g). The fish were fed diets supplemented with Hilyses at concentrations of 0, 1, 2, or 3 g/kg for a period of 8 weeks. The results showed that supplementation with Hilyses at levels up to 2 g/kg diet significantly improved final body weight, weight gain, specific growth rate, feed efficiency ratio, protein efficiency ratio, apparent protein utilization, and energy utilization compared to the control diet without Hilyses. Carcass crude protein content and moisture were significantly higher in Hilyses-fed groups, while crude lipid content decreased at the 3 g/kg supplementation level. Hilyses supplementation enhanced various hematological parameters, including increased red blood cell count, total leukocyte count, hemoglobin concentration, hematocrit, and mean corpuscular volume. Serum biochemistry and immune function markers like total protein, albumin, complement component C3, IgM, and IgG were significantly elevated in the 2 and 3 g/kg Hilyses groups. Antioxidant enzyme activities (catalase, glutathione peroxidase, total superoxide dismutase) were enhanced, and lipid peroxidation was reduced, in the 2 g/kg Hilyses group. Digestive enzyme activities, particularly protease and lipase, were also improved with Hilyses supplementation. Histological examination showed reduced lipid deposition in the liver and increased branching of intestinal villi at the 2 g/kg Hilyses level. Overall, these results indicated that dietary Hilyses supplementation at 2 g/kg diet optimizes growth, feed utilization, nutrient composition, hematology, immunity, antioxidant status, and digestive function in juvenile Nile tilapia.


Subject(s)
Animal Feed , Antioxidants , Cichlids , Dietary Supplements , Fermentation , Intestines , Saccharomyces cerevisiae , Animals , Cichlids/growth & development , Cichlids/immunology , Cichlids/metabolism , Antioxidants/metabolism , Animal Feed/analysis , Intestines/drug effects , Intestines/immunology
4.
Article in English | MEDLINE | ID: mdl-38629380

ABSTRACT

BACKGROUND: The annual incidence of peptic ulcer disease is estimated to be four million cases worldwide, with an average lifetime risk of 7.5% in individuals of all ages. Polymer nanocomposites have novel prospects in the field of modern medicine. OBJECTIVE: The present research endeavors to assess the therapeutic efficacy of nanoparticles composed of silver/chitosan, silver/saponin, and chitosan/saponin against gastric ulcers induced by ethanol in Wistar rats. METHODS: Forty-eight rats were randomly split into eight groups of the same size. Oral ethanol (5 ml/kg of body weight) was given to all rat groups except the control one for 1 hour before treatment. Control and ulcer groups of rats were given distilled water orally. The rats in the other groups were given orally 1/10 LD50 of each treatment as follows: AgNPs, chitosan NPs, Saponin, AgNPs-Chitosan NPs, AgNP-Saponin, and chitosan-Saponin NPs. RESULTS: NP-treated groups showed a significant increase in the gastric juice pH, glutathione reduced, catalase, and nitric oxide while gastric juice volume, ulcer index, and malondialdehyde levels decreased compared with the ulcer group. Histopathological investigation of stomach showed improvement in NPs groups specially in the chitosan-Saponin NPs group. CONCLUSION: The current study revealed that silver-chitosan, silver-saponin and chitosansaponin nanocomposites effectively treat gastric ulcers. Chitosan-Saponin nanoparticles showed high therapeutic effectiveness against gastric ulcer in rats.

5.
Sci Rep ; 14(1): 9144, 2024 04 21.
Article in English | MEDLINE | ID: mdl-38644378

ABSTRACT

In this research, different Co2+ doped ZnO nanoparticles (NPs) were hydrothermally synthesized by an environmentally friendly, sustainable technique using the extract of P. capillacea for the first time. Co-ZnO was characterized and confirmed by FTIR, XPS, XRD, BET, EDX, SEM, TEM, DRS UV-Vis spectroscopy, and TGA analyses. Dislocation density, micro strains, lattice parameters and volume of the unit cell were measured using XRD results. XRD suggests that the average size of these NPs was between 44.49 and 65.69 nm with a hexagonal wurtzite structure. Tauc plot displayed that the optical energy bandgap of ZnO NPs (3.18) slowly declines with Co doping (2.96 eV). Near complete removal of the ciprofloxacin (CIPF) antibiotic was attained using Green 5% of Hy-Co-ZnO in the existence of visible LED light which exhibited maximum degradation efficiency (99%) within 120 min for 30 ppm CIPF initial concentration. The photodegradation mechanism of CIPF using Green Hy-Co-ZnO NPs followed the Pseudo-first-order kinetics. The Green Hy-Co-ZnO NPs improved photocatalytic performance toward CIPF for 3 cycles. The experiments were designed using the RSM (CCD) method for selected parameters such as catalyst dosage, antibiotic dosage, shaking speed, and pH. The maximal CIPF degradation efficiency (96.4%) was achieved under optimum conditions of 39.45 ppm CIPF dosage, 60.56 mg catalyst dosage, 177.33 rpm shaking speed and pH 7.57.


Subject(s)
Anti-Bacterial Agents , Ciprofloxacin , Cobalt , Light , Photolysis , Zinc Oxide , Zinc Oxide/chemistry , Ciprofloxacin/chemistry , Cobalt/chemistry , Anti-Bacterial Agents/chemistry , Metal Nanoparticles/chemistry , Green Chemistry Technology/methods , Nanoparticles/chemistry , Kinetics , Catalysis
6.
Sci Rep ; 14(1): 2016, 2024 Jan 23.
Article in English | MEDLINE | ID: mdl-38263230

ABSTRACT

Photodegradation is considered a significant method engaged for the elimination of organic pollutants from water. In this work, hydrothermal cobalt-doped zinc oxide nanoparticles (Hy-Co-ZnO NPs) loaded with 5, 10, and 15% cobalt were prepared in a hydrothermal way and were investigated as a photocatalyst for the Ciprofloxacin (CIPF) degradation under visible irradiation using LED-light. Characterization approaches such as FTIR, XRD, XPS, DRS UV-vis spectroscopy, SEM, TEM, BET, EDX and TGA were used for the investigation of the fabricated Hy-Co-ZnO NPs. The studies indicated that 10% Hy-Co-ZnO NPs was the most efficient catalyst for the CIPF photolysis compared to ZnO NPs and other Hy-Co-ZnO NPs with 5 and 15% cobalt content. Higher photocatalytic activity (> 98%) of 20 mg/L of CIPF solution was attained within 60 min. The reaction kinetics showed that the first-order model is suitable for displaying the rate of reaction and amount of CIPF elimination with R2 = 0.9883. Moreover, Central composite design (CCD) optimization of the 10% Hy-Co-ZnO NPs was also studied.

7.
Sci Rep ; 13(1): 19329, 2023 Nov 07.
Article in English | MEDLINE | ID: mdl-37935868

ABSTRACT

From the perspective of environmental protection, the highly efficient degradation of antibiotics and organic dyes in wastewater needs to be tackled as soon as possible. In this study, an ecofriendly and green cube-shaped cobalt-doped zinc oxide nanoparticles (Co-ZnO NPs) photocatalyst using Pterocladia Capillacea (P. Capillacea) water extract loaded with 5, 10, and 15% cobalt ions were formed via co-precipitation process to degrade antibiotics. The prepared Co-ZnO NPs were tested as a photocatalyst for the photodegradation of ciprofloxacin (CIPF) in the presence of a visible LED-light source. Co-ZnO NPs have been obtained through the co-precipitation method in the presence of P. Capillacea extract as a green capping agent and reducing agent, for the first time. Several characterization techniques including FTIR, XRD, BET, XPS, TEM, EDX, SEM, TGA and DRS UV-Vis spectroscopy were applied to study the prepared Co-ZnO NPs. XRD results suggested that the average size of these NPs ranged between 42.82 and 46.02 nm with a hexagonal wurtzite structure. Tauc plot shows that the optical energy bandgap of ZnO NPs (3.19 eV) gradually decreases to 2.92 eV by Co doping. Examinations showed that 5% Co-ZnO NPs was the highest efficient catalyst for the CIPF photodegradation when compared with ZnO NPs and other 10 and 15% Co-ZnO NPs. A 10 mg/L solution of CIPF was photo-degraded (100%) within the first 15 min irradiation. The kinetics showed that the first-order model is suitable for displaying the rate of reaction and amount of CIPF elimination with R2 = 0.952. Moreover, central composite design optimization of the 5% Co-doped ZnO NPs was also investigated.

8.
BMC Biotechnol ; 23(1): 28, 2023 08 03.
Article in English | MEDLINE | ID: mdl-37537554

ABSTRACT

BACKGROUND: Coelomic fluid, a pharmacologically active compound in earthworms, exhibits a range of biological activities, including antioxidant, anti-inflammatory, and anticancer. However, the biological activities exerted by the coelomic fluid can be restrained by its low bioavailability and stability. Liposomes are progressively utilized as an entrapment system for natural bioactive compounds with poor bioavailability and stability, which could be appropriate for coelomic fluid. Thus, the present study was designed to fabricate, characterize, and evaluate the stability of liposomal formulation for Allolobophora caliginosa coelomic fluid (ACCF) as a natural antioxidant compound. METHODS: The ACCF-liposomes were developed with a subsequent characterization of their physicochemical attributes. The physical stability, ACCF release behavior, and gastrointestinal stability were evaluated in vitro. The biological activities of ACCF and its liposomal formulation were also determined. RESULTS: The liposomal formulation of ACCF had a steady characteristic absorption band at 201 nm and a transmittance of 99.20 ± 0.10%. Its average hydrodynamic particle size was 98 nm, with a PDI of 0.29 ± 0.04 and a negative zeta potential (-38.66 ± 0.33mV). TEM further confirmed the formation of vesicular, spherical nano-liposomes with unilamellar configuration. Additionally, a remarkable entrapment efficiency percent (77.58 ± 0.82%) with a permeability rate equal to 3.20 ± 0.31% and a high retention rate (54.16 ± 2.20%) for ACCF-liposomes were observed. The Fourier transform infrared spectroscopy (FTIR) result demonstrated that ACCF successfully entrapped inside liposomes. The ACCF-liposomes exhibited a slow and controlled ACCF release in vitro. Regarding stability studies, the liposomal formulation enhanced the stability of ACCF during storage and at different pH. Furthermore, ACCF-liposomes are highly stable in intestinal digestion conditions comparable to gastric digestion. The current study disclosed that liposomal formulation potentiates the biological activities of ACCF, especially antioxidant, anti-inflammatory, and thrombolytic activities. CONCLUSION: These promising results offer a novel approach to increasing the bioaccessibility of ACCF, which may be crucial for the development of pharmaceuticals and nutraceutical-enriched functional foods.


Subject(s)
Liposomes , Oligochaeta , Animals , Liposomes/chemistry , Antioxidants/pharmacology , Anti-Inflammatory Agents/pharmacology , Dietary Supplements , Particle Size
9.
Tissue Cell ; 82: 102118, 2023 Jun.
Article in English | MEDLINE | ID: mdl-37269556

ABSTRACT

Various therapeutic approaches are conducted for regression of liver fibrosis and prevent possible further carcinogenic transformation. This study was aimed to assess the prospective therapeutic potential of bromelain against thioacetamide (TAA)-induced liver fibrosis using in-vitro and in vivo approaches. In vitro study, HSC-T6 cell line was used to evaluate the effect of bromelain on HSC-T6 cell viability and apoptosis. In vivo, Rats were treated by TAA for 6 weeks for induction of hepatic fibrosis followed by post treatment by different doses of bromelain and silymarin for further 4 weeks to assess the regression of hepatic fibrosis. The in-vitro findings indicated that bromelain hindered the proliferation of HSCs in concentration dependent manner compared with the untreated cells. The in vivo study revealed that treatment of TAA fibrotic rats with different doses of bromelain and silymarin induced a significant restoration in liver function biomarkers, attenuation of oxidative stress, upregulation of total antioxidant capacity and thereby decline of fibrotic biomarkers and improving histopathological and immunohistochemical changes. In conclusion, This study indicates that bromelain can regress TAA induced hepatic fibrosis in rats via inhibiting HSCs activation, α-SMA expression and the ECM deposition in hepatic tissue in addition to its antioxidants pathway, these findings prove the promising therapeutic potential of bromelain as a novel therapeutic approach for chronic hepatic fibrotic diseases.


Subject(s)
Hepatic Stellate Cells , Silymarin , Rats , Animals , Hepatic Stellate Cells/metabolism , Bromelains/pharmacology , Bromelains/metabolism , Bromelains/therapeutic use , Liver Cirrhosis/chemically induced , Liver Cirrhosis/drug therapy , Liver/pathology , Antioxidants/metabolism , Silymarin/pharmacology , Silymarin/metabolism , Silymarin/therapeutic use , Biomarkers/metabolism , Thioacetamide/toxicity
10.
Saudi Dent J ; 35(1): 46-52, 2023 Jan.
Article in English | MEDLINE | ID: mdl-36817023

ABSTRACT

Purpose: To compare the nanoleakage between bulkfill and incremental-fill resin composites in class II slot preparations for primary and permanent teeth restored by the snowplow technique. Materials and Methods: Class II slots were prepared in 32 M (16 exfoliated/extracted primary and 16 permanent molars). Optibond All-InOne self-etching adhesive was applied and cured. A flowable composite, Premise, was then injected into the gingival seat without curing using the snowplow technique. Cavities were restored using Sonicfill/bulkfill or microhybrid Herculite composites. Energy dispersive X-ray spectrometry was used to assess nanoleakage as silver deposition percentages along the axial and cervical walls. Multivariate analysis of variance was used to assess the effect of tooth type (primary and permanent teeth) and placement technique (bulkfill and incremental techniques) on nanoleakage at the axial and cervical walls. Results: Bulkfill restorations had significantly greater nanoleakage than incremental restorations at the cervical walls in primary and permanent molars (mean = 1.21 vs 0.49 in primary molars and 0.76 vs 0.24 in permanent molars). Equivalent results were observed at the axial walls of the restorations (mean = 0.66 vs 0.14 in primary molars and 0.28 vs 0.08 in permanent molars, with a P value of<0.001). Conclusions: Less nanoleakage was observed in class II slot/snowplow resin-composite restorations using the incremental technique compared to bulkfill in both dentitions. However, greater nanoleakage was detected on the cervical walls when compared with the axial walls.

11.
Curr Drug Deliv ; 20(5): 575-586, 2023.
Article in English | MEDLINE | ID: mdl-35579149

ABSTRACT

BACKGROUND: Colorectal cancer is one of the most serious gastrointestinal cancers in Africa and its prevention is a pronounced challenge in contemporary medicine worldwide. OBJECTIVE: The present study aimed to develop nanoemulsion drug delivery system using pomegranate polysaccharides (PGPs) as an alternative cancer remedy, and then the evaluated its biological activities. METHODS: The PGPs yield and chemical composition were evaluated, and then a PGPs nanoemulsion (PGPs-NE) was prepared using the self-emulsification technique with an oil phase. The physicochemical characterization of PGPs-NE was then analyzed. The in vitro antioxidant, anti-inflammatory activities, and antitumor potency of PGPs and PGPs-NE were also evaluated. RESULTS: The PGPs yield was 10%. The total sugar and protein content of PGPs was 44.66 mg/dl and 19.83µg/ml, respectively. PGPs were mainly composed of five monosaccharides including fructose, glucose, galactose, rhamnose, and arabinose. Concerning physiochemical characterization, the formulated PGPs-NE had three optical absorption bands at 202, 204, and 207nm and a transmittance of 80%. Its average hydrodynamic particle size was 9.5nm, with a PDI of less than 0.2 and a negative zeta potential (-30.6 mV). The spherical shape of PGPs-NE was confirmed by a transmission electron microscope study, with an average size of less than 50 nm. Additionally, the method used to prepare the PGPs-NE formulation provided high entrapment efficiency (92.82%). The current study disclosed that PGPs-NE exhibited strong antioxidant, anti-inflammatory, and antitumor agent potency compared to that of free PGPs. CONCLUSION: These promising current findings provide evidence for the possible efficacy of novel PGPs-NE as an alternative treatment for CRC.


Subject(s)
Antineoplastic Agents , Nanoparticles , Pomegranate , Antioxidants/pharmacology , Drug Delivery Systems , Antineoplastic Agents/pharmacology , Anti-Inflammatory Agents/pharmacology , Emulsions/chemistry , Particle Size , Nanoparticles/chemistry
12.
BMC Oral Health ; 22(1): 411, 2022 09 19.
Article in English | MEDLINE | ID: mdl-36123671

ABSTRACT

BACKGROUND: Children with cerebral palsy (CP) are at high risk for dental caries. Alteration of some salivary properties encountered among them compared to healthy children, could play a role in this elevated risk. OBJECTIVES: The aim of the present study was to assess salivary physicochemical properties; including total antioxidant (TAC), flow rate, viscosity, pH and buffering capacity, as well as Streptococcus mutans level among children with CP, also to correlate these variables to their caries experience. MATERIALS AND METHODS: This case control study included 80 children with CP, study group (SG) and matched number of healthy children for control group (CG). Interview-based questionnaire, clinical examination, salivary biochemical and microbiological investigations using MALDI-TOF were done. RESULTS: In SG, the caries experience in primary teeth dmft and S. mutans log value were significantly higher than CG (P = 0.039, P = 0.002) while unstimulated salivary flow rate, buffering capacity and salivary TAC were significantly lower (P < 0.0001). Multivariate linear regression showed that the presence of CP was significantly associated with the greatest variation in caries experience in the primary teeth and permanent teeth. Higher unstimulated salivary flow rate, or an increase in buffering capacity by 1 ml of acid/ml of saliva were associated with lower number of the affected primary and permanent teeth. On the other hand, One-unit increase in S. mutans log count and higher salivary TAC were associated with higher caries experience. CONCLUSION: Children with CP have higher caries experience (dmf) due to lower salivary protective factors and higher S. mutans counts.


Subject(s)
Cerebral Palsy , Dental Caries , Antioxidants , Case-Control Studies , Child , Dental Caries/complications , Egypt , Humans , Streptococcus mutans
13.
J Food Biochem ; 46(9): e14296, 2022 09.
Article in English | MEDLINE | ID: mdl-35791516

ABSTRACT

Myocardial infarction (MI) is one of the most prevalent disorders seen in clinical practice, and its prevalence has risen dramatically in the last decade. Ovothiol-A is a natural product isolated from sea urchin eggs and display unusual antioxidant properties. The present study investigates the therapeutic effect of Ovothiol-A against MI stimulated in rats by epinephrine injection. Subcutaneous injection of 2 mg/kg epinephrine for 2 days caused MI in rats. The rats divided into three groups; control, MI, and MI treated with Ovothiol-A (500 mg/kg, orally) for 7 days. The treatment with Ovothiol-A restored ST-segment near normal, ameliorated the changes in cardiac troponin T, creatine kinase, lactate dehydrogenase, aspartate aminotransferase, alanine amino transferase, alkaline phosphatase, total proteins, creatinine, uric acid, urea, malondialdehyde, nitric oxide, reduced glutathione, catalase, glutathione-S-transferase, hemoglobin, RBCs, WBCs, platelet/lymphocyte ratio, and neutrophil/lymphocyte ratio. The histological investigation revealed that Ovothiol-A-treated group showed marked improvement in the examined cardiac muscles, liver and kidney in numerous sections. Ovothiol-A possessed a therapeutic effect against epinephrine-induced myocardial infarction. Ovothiol-A improves cardiac, liver, and kidney biomarkers and restores the typical pattern of EEG. PRACTICAL APPLICATIONS: Eggs of sea urchins are rich in potent antioxidant molecule (Ovothiol-A). The current study reveals the ability to use Ovothiol-A in the treatment of myocardial infarction.


Subject(s)
Antioxidants , Myocardial Infarction , Animals , Antioxidants/metabolism , Aspartate Aminotransferases , Epinephrine/adverse effects , Methylhistidines , Myocardial Infarction/chemically induced , Myocardial Infarction/drug therapy , Rats
14.
J Osteopath Med ; 122(8): 411-422, 2022 05 02.
Article in English | MEDLINE | ID: mdl-35488711

ABSTRACT

CONTEXT: Research is lacking regarding osteopathic approaches in treating polycystic ovary syndrome (PCOS), one of the prevailing endocrine abnormalities in reproductive-aged women. Limited movement of pelvic organs can result in functional and structural deficits, which can be resolved by applying visceral manipulation (VM). OBJECTIVES: This study aims to analyze the effect of VM on dysmenorrhea, irregular, delayed, and/or absent menses, and premenstrual symptoms in PCOS patients. METHODS: Thirty Egyptian women with PCOS, with menstruation-related complaints and free from systematic diseases and/or adrenal gland abnormalities, prospectively participated in a single-blinded, randomized controlled trial. They were recruited from the women's health outpatient clinic in the faculty of physical therapy at Cairo University, with an age of 20-34 years, and a body mass index (BMI) ≥25, <30 kg/m2. Patients were randomly allocated into two equal groups (15 patients); the control group received a low-calorie diet for 3 months, and the study group that received the same hypocaloric diet added to VM to the pelvic organs and their related structures, according to assessment findings, for eight sessions over 3 months. Evaluations for body weight, BMI, and menstrual problems were done by weight-height scale, and menstruation-domain of Polycystic Ovary Syndrome Health-Related Quality of Life Questionnaire (PCOSQ), respectively, at baseline and after 3 months from interventions. Data were described as mean, standard deviation, range, and percentage whenever applicable. RESULTS: Of 60 Egyptian women with PCOS, 30 patients were included, with baseline mean age, weight, BMI, and menstruation domain score of 27.5 ± 2.2 years, 77.7 ± 4.3 kg, 28.6 ± 0.7 kg/m2, and 3.4 ± 1.0, respectively, for the control group, and 26.2 ± 4.7 years, 74.6 ± 3.5 kg, 28.2 ± 1.1 kg/m2, and 2.9 ± 1.0, respectively, for the study group. Out of the 15 patients in the study group, uterine adhesions were found in 14 patients (93.3%), followed by restricted uterine mobility in 13 patients (86.7%), restricted ovarian/broad ligament mobility (9, 60%), and restricted motility (6, 40%). At baseline, there was no significant difference (p>0.05) in any of demographics (age, height), or dependent variables (weight, BMI, menstruation domain score) among both groups. Poststudy, there was a statistically significant reduction (p=0.000) in weight, and BMI mean values for the diet group (71.2 ± 4.2 kg, and 26.4 ± 0.8 kg/m2, respectively) and the diet + VM group (69.2 ± 3.7 kg; 26.1 ± 0.9 kg/m2, respectively). For the improvement in the menstrual complaints, a significant increase (p<0.05) in the menstruation domain mean score was shown in diet group (3.9 ± 1.0), and the diet + VM group (4.6 ± 0.5). On comparing both groups poststudy, there was a statistically significant improvement (p=0.024) in the severity of menstruation-related problems in favor of the diet + VM group. CONCLUSIONS: VM yielded greater improvement in menstrual pain, irregularities, and premenstrual symptoms in PCOS patients when added to caloric restriction than utilizing the low-calorie diet alone in treating that condition.


Subject(s)
Polycystic Ovary Syndrome , Adult , Diet, Reducing , Female , Humans , Menstruation , Menstruation Disturbances/therapy , Obesity , Polycystic Ovary Syndrome/complications , Polycystic Ovary Syndrome/therapy , Quality of Life , Young Adult
15.
Eur Rev Med Pharmacol Sci ; 26(7): 2627-2630, 2022 04.
Article in English | MEDLINE | ID: mdl-35442478

ABSTRACT

The COVID-19 virus has been responsible for the development of several systemic diseases. Recently, the COVID-19 vaccine has also been incriminated in the development of autoimmune diseases. Currently, researchers have focused on the relationship between the COVID-19 vaccine and the activation of autoimmune phenomenon. We report a case of Graves' disease (GD) whose symptoms appeared 3 days after vaccination against COVID-19. A forty-three-year-old female, without pathological history, presented with diarrhea and palpitation. She received her first SARS-CoV-2 Vaccine dose (Pfizer-BioNTech), in August 2021. Three days after the vaccine, she felt palpitations, sleep disorders, muscle weakness, and heat intolerance. On examination, her pulse was 119 beats per minute, she weighed 63 kg, and she had lost 4 kg in only two months. GD was suspected. Thyroid hormone testing showed low thyroid-stimulating hormone, and an elevated serum free thyroxine hormone T4 level. Serology tests were positive for TSH receptor autoantibodies (TRAB). A GD induced by adjuvants of SARS-CoV-2 vaccine has been retained as a final diagnosis. Several autoimmune diseases have been attributed to adjuvant-induced autoimmune/inflammatory syndrome, including systemic sclerosis, systemic lupus erythematosus and rheumatoid arthritis, and recently few cases of GD have been explained by this phenomenon.


Subject(s)
COVID-19 , Graves Disease , Adjuvants, Immunologic , Adult , COVID-19/prevention & control , COVID-19 Vaccines/adverse effects , Female , Graves Disease/diagnosis , Humans , Receptors, Thyrotropin , SARS-CoV-2
16.
Arch Pharm (Weinheim) ; 355(5): e2100454, 2022 May.
Article in English | MEDLINE | ID: mdl-35174895

ABSTRACT

Cancer is the world's foremost cause of death. There are over 100 different forms of cancer. Cancers are frequently named after the organs or tissues in which they develop. As a part of our aim to develop promising anticancer agents, a series of new indeno[1,2-b]quinoxaline derivatives were synthesized. All of the synthesized compounds were tested for anticancer activity in vitro in three human cancer cell lines: the HCT-116 colon cancer cell line, the HepG-2 liver cancer cell line, and the MCF-7 breast cancer cell line. Among the tested derivatives, 2, 3, 5, 12, 21, and 22 showed exceptional antiproliferative activities against the three tested cell lines compared to the reference standard imatinib. These compounds were, therefore, selected for further investigations. Evaluation of their cytotoxicity against a normal human cell line (WI-38) was performed, to ensure their safety and selectivity (IC50 > 92 µM). Then, induction of apoptosis by the most active compounds was found to be accomplished by downregulation of Bcl-2 and upregulation of BAX and caspase-3. After that, the most promising apoptotic compound that increases the caspase-3 and BAX expression and downregulates Bcl-2 activity (3) was assessed for its impact on the cell cycle distribution in HepG-2 cells: The most potent derivative (3) induced cell cycle arrest at the G2/M phase. Finally, in silico evaluation of the ADME properties indicated that compound 3 is orally bioavailable and can be readily synthesized on a large scale.


Subject(s)
Antineoplastic Agents , Neoplasms , Antineoplastic Agents/metabolism , Antineoplastic Agents/pharmacology , Apoptosis , Caspase 3/metabolism , Cell Line, Tumor , Cell Proliferation , Down-Regulation , Drug Screening Assays, Antitumor , Humans , Quinoxalines/pharmacology , Structure-Activity Relationship , Up-Regulation , bcl-2-Associated X Protein/metabolism , bcl-2-Associated X Protein/pharmacology
17.
J Food Biochem ; 46(3): e13729, 2022 03.
Article in English | MEDLINE | ID: mdl-33871886

ABSTRACT

The current study aimed to evaluate the antibacterial, anti-inflammatory, analgesic, and renoprotective effects of echinochrome pigment extracted from sea urchin. The disk diffusion method was used for the antibacterial activity of echinochrome against four different bacterial strains; Salmonella typhimurium, Pseudomonas aeroginosa, Staphylococcus aureus, and Listeria monocytogenes. While, acetic acid-induced writhing, formalin-induced licking, and hot plate latency assays evaluate the analgesic activity. The biochemical and oxidative stress markers of kidneys, as well as the histopathological examination, were measured to evaluate the renoprotective activity of echinochrome for cecal ligation and puncture-induced renal injury in rats. Echinochrome pigment exhibited in vitro antibacterial activity against all aforementioned bacterial species besides a powerful anti-inflammatory impact in vitro by the effective stabilization of the RBCs membrane and in vivo by decrease levels of serum IL6 and TNF-α. What's more, echinochrome showed a notable analgesic efficacy as well as an enhancement of the kidney's biochemical markers, oxidative stress status, and histopathological screening. Ech attenuated cecal ligation and puncture-induced renal injury by improving renal biomarkers, suppressing reactive oxygen species propagation as well as its antibacterial, anti-inflammatory, and anti-nociceptive activities. PRACTICAL APPLICATIONS: Sea urchins are rich in pharmacologically important quinone pigments, specifically echinochrome. The current study aimed to evaluate the role of echinochrome as a renal protective remedy in sepsis and clarify its biological activities. Echinochrome exhibited antibacterial activity in vitro against Salmonella typhimurium, Pseudomonas aeroginosa, Staphylococcus aureus, and Listeria monocytogenes. Our results revealed that echinochrome protects the kidney against damage caused by sepsis in rats. Echinochrome can use in the treatment of sepsis as an antibacterial, anti-inflammatory, and antioxidant agent.


Subject(s)
Nociception , Sepsis , Animals , Anti-Bacterial Agents/pharmacology , Anti-Inflammatory Agents/pharmacology , Inflammation/drug therapy , Kidney , Oxidative Stress , Rats , Sea Urchins , Sepsis/complications , Sepsis/drug therapy , Sepsis/pathology
18.
Front Psychol ; 12: 792446, 2021.
Article in English | MEDLINE | ID: mdl-34899545

ABSTRACT

High-heeled shoes adversely affect spinal curvature, increase the risk of low back pain, and disturb the normal gait pattern. The purpose of this study was to examine, from a biopsychosocial point of view, the combined effect of wearing two different heel heights and of hormonal oscillation throughout different phases of the menstrual cycle on spinopelvic alignment. Notably, 70 females with an average age of 20.42 ± 1.51 years participated in this study, wearing each female two different heel heights as follows: low (2.5 cm) and high (7 cm). Spinopelvic alignment was evaluated by rasterstereography formetric 3D analysis during early follicular, ovulatory, and mid-luteal phases of the menstrual cycle. Statistical analysis showed that there was no significant difference (p > 0.05) on spinopelvic alignment [kyphotic angle (KA), trunk inclination (TI), and pelvic inclination] between wearing low- or high-heeled shoes during early follicular, ovulatory, and mid-luteal phases of the menstrual cycle. Considering that high-heeled shoes are traditionally associated with femininity, body image, beauty, and charm, this research has important biopsychosocial implications that should be explored in detail in future studies.

19.
Bioorg Chem ; 110: 104803, 2021 05.
Article in English | MEDLINE | ID: mdl-33761314

ABSTRACT

One of the best ways to design new biocidal agents is synthesizing hybrid molecules by combining two or more bioactive moieties in a single molecular scaffold. So, new series of quinolines bearing a thiazole moiety were synthesized using thiosemicarbazones 2a-f. Cyclization of 2a-f with ethyl chloroacetate, ethyl 2-chloropropanoate or chloroacetone afforded the corresponding thiazoles 3-5. The antimicrobial activity of the new quinoline derivatives was evaluated. The most of tested compounds revealed potent both of the antibacterial and antifungal activities. Fourfold potency of amphotericin B for the inhibition the growth of the A. fumigatus was displayed by ccompound 5e. The latter compound displayed twofold potency of gentamycin for inhibition the growth of N. gonorrhoeae. Moreover, this compound showed equipotent potency of references drugs for inhibition of the growth of S. flexneri, S. pyogenes, P. vulgaris, A. clavatus, G. candidum and P. marneffei. So, quinolines bearing a thiazole moiety can be suggested as interesting scaffolds for the development both of the novel antibacterial and antifungal agents. Some new derivatives were studied as peptide deformylase enzyme inhibitors. Thiazolidin-4-one derivative 3d and 2,3-dihydrothiazole derivative 5c had shown good PDF inhibition activity, which had been supported by the docking results with highest binding affinity and lowest docking energy score. These results suggested that the most potent compounds might be possible agents as novel bacterial PDF inhibitor.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antifungal Agents/pharmacology , Bacteria/drug effects , Fungi/drug effects , Quinolines/pharmacology , Thiazoles/pharmacology , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/chemistry , Antifungal Agents/chemical synthesis , Antifungal Agents/chemistry , Dose-Response Relationship, Drug , Microbial Sensitivity Tests , Models, Molecular , Molecular Structure , Quinolines/chemistry , Structure-Activity Relationship , Thiazoles/chemistry
20.
Pathogens ; 10(2)2021 Feb 09.
Article in English | MEDLINE | ID: mdl-33572193

ABSTRACT

Using synthetic antibiotics/chemicals for infectious bacterial pathogens and parasitic disease control causes beneficial microbial killing, produces multi-drug resistant pathogens, and residual antibiotic impacts in humans are the major threats to aquaculture sustainability. Applications of herbal products to combat microbial and parasitic diseases are considered as alternative approaches for sustainable aquaculture. Essential oils (EOs) are the secondary metabolites of medicinal plants that possess bioactive compounds like terpens, terpenoids, phenylpropenes, and isothiocyanates with synergistic relationship among these compounds. The hydrophobic compounds of EOs can penetrate the bacterial and parasitic cells and cause cell deformities and organelles dysfunctions. Dietary supplementation of EOs also modulate growth, immunity, and infectious disease resistance in aquatic organisms. Published research reports also demonstrated EOs effectiveness against Ichthyophthirius multifiliis, Gyrodactylus sp., Euclinostomum heterostomum, and other parasites both in vivo and in vitro. Moreover, different infectious fish pathogenic bacteria like Aeromonas salmonicida, Vibrio harveyi, and Streptococcus agalactiae destruction was confirmed by plant originated EOs. However, no research was conducted to confirm the mechanism of action or pathway identification of EOs to combat aquatic parasites and disease-causing microbes. This review aims to explore the effectiveness of EOs against fish parasites and pathogenic bacteria as an environment-friendly phytotherapeutic in the aquaculture industry. Moreover, research gaps and future approaches to use EOs for sustainable aquaculture practice are also postulated.

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