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1.
Eur J Pharmacol ; 913: 174590, 2021 Dec 15.
Article in English | MEDLINE | ID: mdl-34801530

ABSTRACT

Nutraceuticals are principally extracted from natural products that are frequently safe and well-tolerated. Lycopene and berberine are natural plants with a wide range of beneficial effects including protective activities against metabolic disorders such as diabetes and cardiovascular diseases. These compounds might be considered technically more as a drug than a nutraceutical and could be prescribed as a product. However, further studies are needed to understand if these supplements could affect metabolic syndrome outcomes. Even if nutraceuticals exert a prophylactic activity within the body, their bioactivity and bioavailability have high interindividual variation, and precise assessment of biological function of these bioactive compounds in randomized clinical trials is critical. However, these reports must be interpreted with more considerations due to the low quality of the trials. The aim of this paper is to bring evidence about the management of cardiovascular diseases and diabetes through the use of nutraceuticals with particular attention to lycopene and berberine effectiveness.


Subject(s)
Berberine/administration & dosage , Cardiovascular Diseases/therapy , Diabetes Mellitus/therapy , Dietary Supplements , Lycopene/administration & dosage , Berberine/pharmacokinetics , Biological Availability , Combined Modality Therapy/methods , Drug Evaluation, Preclinical , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage , Lycopene/pharmacokinetics , Metformin/administration & dosage , Randomized Controlled Trials as Topic , Treatment Outcome
2.
Anal Biochem ; 629: 114307, 2021 09 15.
Article in English | MEDLINE | ID: mdl-34273317

ABSTRACT

Biosensor technology is considered to be a great alternative in analytical techniques over the conventional methods. Among many recently developed techniques and devices, aptasensors are interesting because of their high specificity, selectivity and sensitivity. Combining aptamer as a biological recognition element with gold nanoparticles (AuNPs) as probe, are becoming more general owing to their beneficial properties, including low cost and ability to analyze specific targets on-site and using naked eye. Hydrogen bonds, nucleic acid hybridization, aptamer-target and antigen-antibody binding, Raman signature, enzyme inhibition, and enzyme-mimicking activity are main different sensing strategies exploited in AuNPs-based optical aptasensors. In this review article, we discussed the recent advances in optical aptasensors with a special emphasis on the catalytic activity property of AuNPs.


Subject(s)
Aptamers, Nucleotide/analysis , Biomimetic Materials/chemistry , Gold/chemistry , Metal Nanoparticles/chemistry , Biosensing Techniques , Catalysis , Enzyme Activation , Humans , Hydrogen Bonding , Limit of Detection , Nucleic Acid Hybridization , Protein Binding , Surface Properties
3.
Spectrochim Acta A Mol Biomol Spectrosc ; 259: 119840, 2021 Oct 05.
Article in English | MEDLINE | ID: mdl-33965888

ABSTRACT

Tramadol hydrochloride (TH), as an atypical opioid and a 4-phenyl-piperidine analogue of codeine, is mainly used for treating moderate to severe pains. Due to its extensive application, the consequent need for its analysis in various samples is essential. The current study focuses on the introduction of a rapid fluorescent assay using graphene oxide (GO) and aptamer for determination of tramadol in serum samples. Specific ssDNA aptamers for TH were developed by SELEX (Systematic Evolution of Ligands by EXponential Enrichment) technique using GO as a fluorescence quencher. After 10 rounds, two aptamers (Apt19 and Apt39) were selected from various families. Then, the binding constants of aptamers were measured using fluorometric assay and finally Apt39 (labeled with ATTO 647N) was chosen for development of a fluorescent aptasensor because this aptamer bound to TH with high affinity (Kd = 178.4 nM) and specificity. The current analytical system showed detection limits of 1.04 nM and 2.56 nM in serum sample and phosphate buffer saline (10 mM PBS), respectively.


Subject(s)
Aptamers, Nucleotide , Graphite , Tramadol , Humans , SELEX Aptamer Technique
4.
Adv Exp Med Biol ; 1286: 115-124, 2021.
Article in English | MEDLINE | ID: mdl-33725349

ABSTRACT

Depression is a mental disorder and a major public health concern affecting millions of people worldwide. It is a common disorder that has been associated with several medical comorbidities often linked with aging, such as dementia, type II diabetes, cardiovascular and cerebrovascular diseases, as well as metabolic syndrome. There are a variety of medications available for depression treatment. Selective serotonin reuptake inhibitors (SSRIs) are one of the antidepressant drug classes that are most widely used to treat depressive disorders and depressive symptoms in other diseases. Due to many contradictory findings on the adverse effects and toxicities of SSRIs (especially genotoxicities), we reviewed the genotoxic effects of these drugs. Based on the guidelines proposed in the PRISMA statement, we performed a systematic review by searching international electronic databases including PubMed, Scopus, Embase, and Web of Science to find the published documents on SSRIs and their genotoxic effects from January 1990 to November 2019. After the removal of 203 duplicate articles, 385 articles were screened and 167 articles met the inclusion criteria and qualified for evaluation of their full texts. After this, 26 articles were appropriate for final review. This revealed that the proportion of genotoxicities was highest for citalopram and fluoxetine, with a smaller proportion for sertraline. Limited documentations showed genotoxic and partial genotoxic effects for paroxetine and escitalopram, respectively. Although a number of studies have found genotoxic effects of SSRIs, there are also some factors including doses, duration of exposure, model of experiments, and the type of technique assay that may affect the results.


Subject(s)
Diabetes Mellitus, Type 2 , Selective Serotonin Reuptake Inhibitors , Citalopram , DNA Damage , Humans , Paroxetine , Selective Serotonin Reuptake Inhibitors/adverse effects
5.
Phytother Res ; 33(12): 3040-3053, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31464016

ABSTRACT

The metabolic syndrome (MetS) is a cluster of multiple conditions that includes hypertension, dyslipidemia, abdominal obesity, and hyperglycemia disorders. Most studies revealed that the MetS is accompanied with an increased risk for cardiovascular disease, Type 2 diabetes mellitus, and insulin resistance. It can be said that, in treating or preventing the MetS and its components, lifestyle adjustment and weight loss have a vital role. According to various studies, among natural compounds, celery (Apium graveolens) is one of the most important sources of phytochemicals such as phenolic acids, flavones, flavonols, and antioxidants such as vitamin C, beta-carotene (Provitamin A), and manganese. These antioxidants have a role in decreasing the oxidative damage. The phytochemicals in celery decrease the activity of proinflammatory cytokines and prevent inflammation. Also, flavonoids in celery suppress cardiovascular inflammation. Oxidative stress and inflammation in the blood stream are the main risk factors in increasing cardiovascular disease, especially atherosclerosis. Celery phthalides leads to expanding of smooth muscle in the blood vessels and lower blood pressure. As a result, the most active ingredients in celery (A. graveolens (have shown hypolipidemic, antidiabetic, and hypotensive properties. In this review, we summarized the mechanisms underlying the protective effects of celery components on insulin action, glucose, lipid metabolism, and blood pressure.


Subject(s)
Apium/chemistry , Metabolic Syndrome/diet therapy , Humans
6.
Biofactors ; 45(1): 5-23, 2019 Jan.
Article in English | MEDLINE | ID: mdl-30339717

ABSTRACT

People are exposed to a number of environmental, occupational, and therapeutic toxic agents which may be natural or man made. These hazardous substances may manifest as direct side effects on the function of organs or indirectly induced alteration of gene expression, cancer-associated metabolic pathways, and/or alter homeostasis. Lycopene, as a one of the most potent antioxidant, is found in fruits and vegetables. High-intake of lycopene has been shown to be effective in decreasing the risk of both natural toxins including mycotoxins, bacterial toxins, and chemical toxins including heavy metals, pesticides as well as herbicides. Recently, there is growing attention in understanding the mechanisms of the phytochemicals and carotenoids as antioxidative, antiapoptotic, radical scavenging, and chelating agents and their roles in the modulation of inflammatory pathways. This review summarizes available data from several recent studies about lycopene and its role against chemical and natural toxicants. © 2018 BioFactors, 45(1):5-23, 2019.


Subject(s)
Antioxidants/pharmacology , Bacterial Toxins/antagonists & inhibitors , Chelating Agents/pharmacology , Lycopene/pharmacology , Mycotoxins/antagonists & inhibitors , Pesticides/antagonists & inhibitors , Animals , Antioxidants/metabolism , Bacterial Toxins/toxicity , Chelating Agents/metabolism , Fluorides/antagonists & inhibitors , Fluorides/toxicity , Food Contamination/analysis , Humans , Lipopolysaccharides/antagonists & inhibitors , Lipopolysaccharides/toxicity , Lycopene/metabolism , Metabolic Networks and Pathways/drug effects , Metabolic Networks and Pathways/genetics , Metals, Heavy/antagonists & inhibitors , Metals, Heavy/toxicity , Mycotoxins/toxicity , Pesticides/toxicity , Rats , Toxicity Tests, Chronic
7.
Cancer Biother Radiopharm ; 26(3): 325-9, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21711107

ABSTRACT

The radioprotective effect of hydroalcholic Zataria multiflora (Avishan-e shirazi) extract was investigated against genotoxicity induced by γ irradiation in human lymphocytes. Peripheral blood samples were collected from human volunteers and incubated with Z. multiflora extract at different concentrations (5, 10, and 50 µg/mL) for 1 hour. At each dose point, the whole blood was exposed in vitro to 150 cGy of cobalt-60 γ irradiation, and then the lymphocytes were cultured with mitogenic stimulation to determine number of the micronuclei in cytokinesis-blocked binucleated cells. The treatment of lymphocytes with extract showed a significant decrease in the incidence of micronuclei binucleated cells, compared with similarly irradiated lymphocytes without extract against γ irradiation. The maximum protection and decrease in frequency of micronuclei was observed at 50 µg/mL of Zataria extract by 32% reduction. High-performance liquid chromatography analysis of extract showed that it contains high amounts of thymol. Zataria extract exhibited concentration-dependent radical-scavenging activity on 1,1-diphenyl-2-picryl hydrazyl free radicals. These data have an important application for the protection of human lymphocyte from the genetic damage and side-effects induced by γ irradiation in personnel exposed to radiation.


Subject(s)
Ferns/metabolism , Lymphocytes/drug effects , Lymphocytes/radiation effects , Plant Extracts/pharmacology , Radiation-Protective Agents/pharmacology , Antioxidants/metabolism , Chromatography, High Pressure Liquid/methods , Cobalt Radioisotopes/pharmacology , DNA Damage/drug effects , Dose-Response Relationship, Drug , Free Radicals , Gamma Rays , Humans , Micronucleus Tests/methods , Time Factors
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