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1.
Heliyon ; 9(11): e21037, 2023 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-37928016

RESUMO

The effects of Na+ substitution by Y3+ on the structural, microstructural, dielectric and electrical properties of Ba2Na(1-3x)YxNb5O15 compositions with (x = 0, 0.02 and 0.04) have been studied in detail. The solid solutions of different compositions were prepared by the solid state reaction route method and characterized by X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Complex Impedance Spectroscopy (CIS) techniques. The XRD study confirmed that all prepared compositions have a single-phase orthorhombic tungsten bronze structure with space group Cmm2 at room temperature. The microstructural studies revealed a grain shape and size change in response to increasing Y3+ concentration. The dielectric properties of the obtained compositions are evaluated over a temperature range of 40-600 °C. The dielectric properties were improved for the Y2O3-substituted Ba2NaNb5O15 compound compared to the undoped Ba2NaNb5O15 compound. The non-Debye type relaxation mechanism is confirmed by the -Z″ versus Z' traces. The grain contribution was studied using an equivalent electrical circuit with a Resistor R, a Capacitor C, and a Constant-Phase Element CPE in parallel, in the absence of the grain boundary response and the electrode effect in the frequency range 10 Hz-1MHz. The experimental AC conductivity data were evaluated by using Jonscher's power law. The activation energies obtained from the relaxation and conduction processes, present two different regions as a function of temperature related to the two electrical processes for the prepared ceramics.

2.
Behav Pharmacol ; 34(6): 330-339, 2023 09 01.
Artigo em Inglês | MEDLINE | ID: mdl-37462147

RESUMO

Stress contributes to numerous psychopathologies, including memory impairment, and threatens one's well-being. It has been reported that creatine supplementation potentially influences cognitive processing. Hence, in this study, we examined the effects of creatine supplementation on memory, synaptic plasticity, and neuronal arborization in the CA1 region of the hippocampus in rats under chronic restraint stress (CRS). Thirty-two adult male Wistar rats (8 weeks old) weighing 200-250 g were randomly divided into four groups (n = 8/per group): control, stress, creatine, and stress + creatine. CRS was induced for 6 h per day for 14 days, and creatine supplementation was carried out by dissolving creatine (2 g/kg body weight per day) in the animals' drinking water for 14 days. We used the Barnes maze and shuttle box for spatial and passive avoidance memory examination. The in-vivo field potential recording and Golgi-Cox staining were also used to investigate long-term potentiation (LTP) and dendrite arborization in the CA1 pyramidal neurons. Chronic stress impaired spatial memory, dysregulated LTP parameters, and decreased the number of dendrites in the CA1 pyramidal neurons of stressed rats, and creatine supplementation modified these effects in stressed rats. It seems that creatine supplementation can improve spatial memory deficits and synaptic plasticity loss induced by CRS in hippocampal CA1 neurons, possibly by reducing the dendrite arborization damages. However, understanding its mechanism needs further investigation.


Assuntos
Creatina , Potenciação de Longa Duração , Ratos , Masculino , Animais , Potenciação de Longa Duração/fisiologia , Creatina/farmacologia , Memória Espacial , Ratos Wistar , Hipocampo , Plasticidade Neuronal , Transtornos da Memória/tratamento farmacológico , Suplementos Nutricionais , Aprendizagem em Labirinto
3.
Clin Nutr ESPEN ; 56: 59-66, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-37344084

RESUMO

BACKGROUND: For years, numerous studies have focused on identifying approaches to increase insulin sensitivity by modifying the signaling factors. In the present study, we examined the effects of Eryngium billardieri extract, as an anti-diabetic herbal medication, on the heart mRNA level of Akt serine/threonine kinase (Akt), mechanistic target of rapamycin kinase (mTOR), peroxisome proliferator-activated receptor gamma (PPARγ), and Forkhead box o1 (Foxo1) in rats with high-fat diet (HFD)-induced insulin resistance (IR). We also assessed the anti-diabetic effects of E. billardieri extract in rats with insulin resistance. METHODS: Twenty-seven male Wistar rats were divided into two groups. Nine rats were fed a normal diet (control group), and 18 rats were fed an HFD for 13 weeks (HFD group). To confirm the induction of insulin resistance, the oral glucose tolerance test (OGTT) was performed and homeostatic model assessment for insulin resistance (HOMA-IR) was calculated. Then rats with IR were randomly divided into the following groups: the HFD group, which continued an HFD, and the group treated with E. billardieri extract, which received the extract at a concentration of 50 mg/kg for 30 days. On the 30th day, the animals were sacrificed and serum samples were collected for biochemistry analyses. Furthermore, the expression of Akt, mTOR, PPARγ, and Foxo1 was measured in heart tissue using the real-time polymerase chain reaction (PCR) method. RESULTS: Real-time PCR analyses revealed that an HFD can significantly decrease the expression level of Akt, mTOR, and PPARγ in the heart tissue. However, an HFD significantly increased the expression level of Foxo1 in the HFD group compared to the control group (P < 0.05). In addition, our data showed that the administration of E. billardieri extract significantly enhanced the mRNA levels of Akt, PPARγ, and mTOR in the heart tissue compared to the HFD group (P < 0.05), while it significantly decreased the Foxo1 mRNA levels (P < 0.01). CONCLUSION: Given that Akt, mTOR, PPARγ, and Foxo1 are critical factors in insulin resistance, the present study suggests that E. billardieri could probably be used as an alternative treatment for IR as a major feature of metabolic syndrome.


Assuntos
Eryngium , Resistência à Insulina , Ratos , Masculino , Animais , Eryngium/metabolismo , Proteínas Proto-Oncogênicas c-akt/genética , Proteínas Proto-Oncogênicas c-akt/metabolismo , PPAR gama/genética , Ratos Wistar , RNA Mensageiro , Serina-Treonina Quinases TOR/genética , Expressão Gênica
4.
Clin Exp Pharmacol Physiol ; 50(4): 298-306, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-36573522

RESUMO

The percutaneous bioavailability of naproxen is low and several technologies have been utilized to overcome the problem. Although, some studies have reported the permeation-enhancing properties of natural essential oils, no research has reflected the effectiveness of Lavandula angustifolia essential oil (LAEO) on increasing the percutaneous absorption of naproxen sodium from a topical gel. Therefore, the present study was designed to investigate whether LAEO increased the percutaneous absorption and the analgesic effects of naproxen sodium topical gel. In the present study, naproxen topical gel was formulated using carbopol 940 (a gelling agent) and several vehicles such as PEG 400, ethanol, and water and the properties of gels were measured. Percutaneous absorption-enhancing properties of LAEO were measured too. Based on our data, the essential oil-containing formulation of naproxen represented greater penetration into (222.19 ± 24.87 vs. 107.65 ± 6.38 µg/cm2 ), and also across (22.07 ± 4.42 vs. 13.14 ± 2.87 µg/cm2 ) skin layers compared to the naproxen gel. Additionally, a significant analgesic property was observed in the naproxen topical gel containing 0.5% essential oil during both first and late phases of formalin test, as well as the late phase of tail-flick test. It could be concluded that LAEO significantly enhanced naproxen percutaneous absorption and also its analgesic effects.


Assuntos
Lavandula , Óleos Voláteis , Absorção Cutânea , Naproxeno , Óleos Voláteis/farmacologia , Géis
5.
RSC Adv ; 12(51): 33124-33141, 2022 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-36425213

RESUMO

This paper presents a systematic study of the substitution effect by lanthanides (Ln3+ = Sm3+ and La3+) in the A-site of perovskite Ba(1-x)Ln2x/3(Ti0.99Zr0.01)O3 with a substitution rate equal to 3.4%. All samples were synthesized by the classical solid-state reaction route and characterized by X-ray diffraction and a complex impedance spectroscopy technique. The synthesized compounds exhibit single-phase perovskite structures without detectable secondary phases. The P4mm space group was verified by the Rietveld method from the X-ray diffraction data, with the tetragonal distortion decreasing with the increasing ionic radius of the lanthanides. SEM micrographs of all ceramics revealed high densification, low porosity and homogeneous distribution of grains of different sizes over the entire surface. The dielectric properties of non-doped and Sm3+ and La3+ doped Ba(1-x)Ln2x/3(Ti0.99Zr0.01)O3 compound are studied in the temperature range of 40-250 °C. The dielectric permittivity ε' increases and the ferroelectric-paraelectric phase transition temperature decreases when the lanthanides are inserted into the A-site of Ba(1-x)Ln2x/3(Ti0.99Zr0.01)O3 perovskite. The Nyquist plots indicate a non-Debye type relaxation process. Conductivity and electrical modulus plots as a function of frequency (10 to 106 Hz) include two electrical responses corresponding to grain and grain boundary effects for all ceramics studied.

6.
Brain Res Bull ; 190: 168-178, 2022 11.
Artigo em Inglês | MEDLINE | ID: mdl-36240907

RESUMO

Patients with chronic pain exhibit anxiety and deficits in memory. Additionally, α2-adrenoceptors that are wildly expressed in the brain have an important role in modulating both pain and memory formation. In the present study, we investigated the interaction effects of crocin with central α2-adrenoceptors on pain comorbidity and hippocampal synaptic plasticity changes following chronic constriction injury (CCI) of the sciatic nerve in rats. All the drugs (crocin, an antagonist (yohimbine) and agonist (clonidine) of α2-adrenergic receptors) were injected (via intracerebroventricular injection) from the day of CCI operation (day 0) and continued daily (once per day) until the 14th day post-CCI. The effects of drugs on the cold allodynia (using acetone test) and anxiety-like behaviors (using elevated plus maze, EPM and open field tests) were assessed. Spatial memory (using Barnes maze) was assessed on day 14 post-CCI operation. Hippocampal synaptic plasticity (using in-vivo extracellular field potential recording) was performed on day 14 post-CCI operation. We observed that crocin induced analgesic, anxiolytic and memory enhancer action following CCI surgery. Furthermore, crocin significantly increased long-term potentiation (LTP) (increased fEPSP slope and population spike amplitude). Furthermore, the co-injection of yohimbine effectively decreased analgesic, anxiolytic and enhancer action of crocin on the LTP parameters (fEPSP slope and population spike amplitude). Our study provided information that protective effects of crocin on pain/anxiety responses and synaptic plasticity were possibly mediated by central α2-adrenoceptor in the rats with chronic pain.


Assuntos
Ansiolíticos , Dor Crônica , Ratos , Animais , Dor Crônica/tratamento farmacológico , Ansiolíticos/farmacologia , Receptores Adrenérgicos alfa 2/metabolismo , Ioimbina/efeitos adversos , Transtornos da Memória/induzido quimicamente , Hipocampo/metabolismo , Potenciação de Longa Duração , Analgésicos/farmacologia , Plasticidade Neuronal
7.
Mol Biol Rep ; 49(11): 10457-10467, 2022 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-36107372

RESUMO

BACKGROUND: Due to the complications related to the use of the current pharmacological approach for the alleviation of neuropathic pain, searching for effective compound with fewer complications is a requirement of the present era. It is well known that the pathophysiological mechanism of neuropathic pain is related to excessive inflammation in the nervous system. Hence, the present study focuses on whether the potential analgesic effects of Terminalia chebula (TC) extract are mediated by the changes in the protein expression of nerve growth factor (NGF) and nuclear factor-kappa B (NF-κB) in the brain in a rat model of sciatic nerve chronic constriction injury (CCI). METHOD AND RESULTS: Neuropathic pain was induced by the left sciatic nerve CCI. Male Wistar rats were assigned to three groups: sham, CCI, and CCI + TC (40 mg/kg). Animals received either normal saline (1 mL) or the aqueous-alcoholic extract of TC (40 mg/kg) for 30 days via gavage needles once a day. Cold allodynia and anxiety-like behaviors were examined one day before CCI surgery (day - 1), as well as days 2, 7, 14, and 30 following CCI. We also assessed the effects of the TC extract oxidative stress markers on day 30 following CCI. Moreover, a western blot analysis was performed on day 30 following CCI to evaluate the effects of the TC extract on the protein expression of NGF and NF-κB in the brain. Oral gavage of the TC extract significantly decreased cold allodynia on days 2 and 14 following CCI. Additionally, the CCI model of chronic pain significantly increased the protein expression of NGF and NF-κB in the brain on day 30 following CCI. Furthermore, the TC extract significantly decreased the protein expression of NGF and NF-κB in the brain. The TC extract also significantly increased the brain glutathione (GSH) content and decreased the malondialdehyde (MDA) content. CONCLUSION: It is suggested that the analgesic effects of the TC extract are mediated by the suppression of brain NGF, NF-κB, and by its antioxidant activity in the brain following neuropathic pain in rats.


Assuntos
Neuralgia , Neuropatia Ciática , Ratos , Animais , Masculino , NF-kappa B/metabolismo , Hiperalgesia/tratamento farmacológico , Fator de Crescimento Neural/genética , Fator de Crescimento Neural/metabolismo , Fator de Crescimento Neural/farmacologia , Ratos Sprague-Dawley , Ratos Wistar , Neuralgia/tratamento farmacológico , Neuralgia/metabolismo , Biomarcadores/metabolismo , Analgésicos/farmacologia , Analgésicos/metabolismo , Encéfalo/metabolismo , Estresse Oxidativo , Nervo Isquiático/lesões
9.
BMC Health Serv Res ; 22(1): 547, 2022 Apr 25.
Artigo em Inglês | MEDLINE | ID: mdl-35462540

RESUMO

AIMS: This study aimed to assess predictors of patient safety competency among emergency nurses. BACKGROUND: The role of emergency nurses is to provide high-quality health care to patients and ensure their safety. The patient safety competency includes the absence of unnecessary or potential harm when providing health care to patients. In providing health care, effective teamwork can affect patient safety and outcomes. Psychological safety is essential to effective teamwork. Psychological safety allows health care workers to accept the interpersonal risks needed to perform effective teamwork and maintain patient safety. METHODS: This study was cross-sectional correlational research. Using convenience sampling methods, 254 emergency department nurses from five educational hospitals were enrolled in the study. Patient Safety in Nursing Education Questionnaire was used to measure the patient safety competency, the teamwork questionnaire to examine the teamwork, and Edmondson psychological safety questionnaire was used to measure psychological safety. Descriptive statistics, t-test, one-way analysis of variance (ANOVA), Pearson's r correlation coefficient, and multivariate stepwise linear regression analysis were applied using SPSS 14.0. RESULTS: Participants' mean patient safety competency score was 2.97 (1-4). Between 18 independent variables evaluated in the multiple regression analysis, seven had a significant effect on the patient safety competency of emergency nurses (R2: 0.39, p < .001). CONCLUSIONS: The patient safety competency of emergency department nurses was primarily related to the structure and leadership of the team and secondary to psychological safety and experience in patient safety activity. The results demonstrated that policymakers and hospital managers should improve and enhance team structure and leadership via supervision and cooperation with the nursing staff. The development of training programs in patient safety activities, improvement, and increase of psychological safety at the levels of the nursing units is essential to increase patient safety competencies in the emergency nursing program.


Assuntos
Enfermagem em Emergência , Segurança do Paciente , Estudos Transversais , Humanos , Irã (Geográfico) , Liderança , Inquéritos e Questionários
10.
Cell Biosci ; 12(1): 4, 2022 Jan 04.
Artigo em Inglês | MEDLINE | ID: mdl-34983649

RESUMO

Although sex hormones play a key role in sex differences in susceptibility, severity, outcomes, and response to therapy of different diseases, sex chromosomes are also increasingly recognized as an important factor. Studies demonstrated that the Y chromosome is not a 'genetic wasteland' and can be a useful genetic marker for interpreting various male-specific physiological and pathophysiological characteristics. Y chromosome harbors male­specific genes, which either solely or in cooperation with their X-counterpart, and independent or in conjunction with sex hormones have a considerable impact on basic physiology and disease mechanisms in most or all tissues development. Furthermore, loss of Y chromosome and/or aberrant expression of Y chromosome genes cause sex differences in disease mechanisms. With the launch of the human proteome project (HPP), the association of Y chromosome proteins with pathological conditions has been increasingly explored. In this review, the involvement of Y chromosome genes in male-specific diseases such as prostate cancer and the cases that are more prevalent in men, such as cardiovascular disease, neurological disease, and cancers, has been highlighted. Understanding the molecular mechanisms underlying Y chromosome-related diseases can have a significant impact on the prevention, diagnosis, and treatment of diseases.

11.
J Complement Integr Med ; 19(2): 203-211, 2022 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-33964199

RESUMO

OBJECTIVES: The neem (Azadirachta indica) have been used in herbal medicine for the treatment of multiple diseases, particularly cancer. The mechanism of anti-cancer properties of neem are far from clear. However, it is well accepted that anti-cancer effects of neem is mediated via its hepatic anti-oxidant activity. In the present review, we are going to classify in vitro and in vivo studies about anti-cancer activity of neem via its hepatic anti-oxidant activity. We also summarize its active ingredients and some therapeutic and toxic dosage forms. METHODS: A systematic search in the literature was performed in PubMed, Scopus, Embase, Cochrane Library, Web of Science, as well as Google Scholar pre-print database using all available MeSH terms for neem, A. indica, anti-cancer, anti-tumor, carcinogen, liver, antioxidant activity, neem ingredients, and glutathione. Electronic database searches combined and duplicates were removed. RESULTS: The neem plant have been used in herbal medicine for the treatment of various diseases, particularly cancer. The mechanisms of anti-cancer effects of neem are far from clear. Cancerous cells growth can induce imbalance the oxidant and anti-oxidant activity in various organs particularly in the liver. Therefore, it seems that neem have anti-cancer effects via restore of the antioxidant disturbances close to the control ones in the liver. Additionally, administration of neem extract can induce oncostatic potential via several mechanism including; suppression of the NF-κß pathway, increased expression of tumor suppressor (such as p53 and pTEN), decreased expression of oncogenes (such as c-Myc), and increased apoptosis in cancerous cells. The median lethal dose (LD50) value for extracts of neem was higher than 2,500 mg/kg. CONCLUSIONS: It is suggested that neem plays pivotal role in the prevention and treatment of cancer via its hepatic antioxidant activity. Indeed, application of neem extract can decreased tumor growth via restore of the antioxidant disturbances close to the control ones in the liver.


Assuntos
Azadirachta , Neoplasias , Antioxidantes/farmacologia , Antioxidantes/uso terapêutico , Biofarmácia , Humanos , Fígado , Neoplasias/tratamento farmacológico , Extratos Vegetais/farmacologia , Extratos Vegetais/uso terapêutico , Folhas de Planta
12.
Braz. arch. biol. technol ; 65: e22210268, 2022. tab
Artigo em Inglês | LILACS | ID: biblio-1364472

RESUMO

Abstract: Sulfur mustard is one of the chemical warfare agent. It rapidly reacts with the cutaneous tissues and other tissues, leading to various devastating long-term effects on human health. Mustard-exposed veterans suffer from its chronic skin problems, including itching, burning sensation, and eczema. We aimed to evaluate the protective effects of Myrtus communis L. (myrtle) on chronic skin lesions and quality of life of sulfur mustard-exposed veterans. In this randomized, double-blind clinical trial, 60 sulfur mustard-exposed patients were evaluated. Thirty patients received myrtle essence 5% cream (case group) and 30 patients received Eucerin cream (placebo group) twice in a day for one month. Then, We assessed the chronic skin problems and itching-related parameters (such as the itching time, severity, distribution, frequency, and calculated itching score), duration of sleep, number of waking up at night, and quality of life in the both groups. Our analysis of data revealed that application of myrtle cream effectively decreased skin problems including; itching and burning sensation. Additionally, myrtle markedly decreased skin lesion symptoms such as excoriation in the case group as compared with before treatment. Noticeably, myrtle cream significantly improved quality of life of the patients in the case group. The present study provides more in-depth information regarding the protective role of myrtle on the sulfur mustard-induces skin complication. Also, myrtle effectively improved quality of life of the sulfur mustard-exposed veterans.


Assuntos
Humanos , Pessoa de Meia-Idade , Dermatopatias/induzido quimicamente , Extratos Vegetais/uso terapêutico , Substâncias para a Guerra Química/toxicidade , Myrtus communis/uso terapêutico , Fitoterapia , Gás de Mostarda/toxicidade , Prurido/induzido quimicamente , Qualidade de Vida , Veteranos , Indicadores de Qualidade de Vida , Eczema/induzido quimicamente , Exposição à Guerra/efeitos adversos , Irã (Geográfico)
13.
Braz. J. Pharm. Sci. (Online) ; 58: e201077, 2022. graf
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1420389

RESUMO

Abstract The present study aims to examine the anti-diabetic effects of fullerene C60 nanoparticle, as an anti-oxidant compound, on serum glucose level, body weight, food and water intake, and pancreatic oxidative stress in the rats with type 1 diabetes. Diabetes mellitus was induced by single intravenous injection of streptozotocine (45 mg/kg) into the tail vein of the rats. Four groups of rats were divided as follow: normal, normal treatment, diabetic, and diabetic treatment groups. Normal treatment and diabetic treatment groups received intra-orally fullerene (1 mg/ kg/daily) up to day 60 following streptozotocine injection. Oxidative stress markers in the pancreas were evaluated on day 60 after inducing diabetes mellitus. Injection of streptozotocine significantly increased serum glucose level as well as food and water intake on all experimental days; it decreased body weight on day 60. Streptozotocine increased MDA level and decreased GSH level and SOD activity in the pancreas. Fullerene significantly decreased food and water intake and increased body weight as compared with the diabetic group. Fullerene also could normalize the pancreatic MDA and GSH markers. The present study suggested that fullerene can decrease diabetic symptoms via its anti-oxidant activity in the pancreas in the rats with type 1 diabetes mellitus.

14.
Brain Res Bull ; 177: 12-21, 2021 12.
Artigo em Inglês | MEDLINE | ID: mdl-34534638

RESUMO

The basolateral nucleus of the amygdala (BLA) is responsible for memory retrieval after stress. It regulates hippocampal long-term potentiation (LTP) during stress. Although ß-adrenoceptors of the BLA have a critical role in memory, few studies have addressed this question in the BLA, and the results still have been contradictory. The present study was designed to investigate the involvement of ß-adrenoceptors of the BLA on hippocampus memory, anxiety, and plasticity in intact and stressed rats. Male Wistar rats were submitted to the electrical foot-shock stress for four consecutive days. Over four consecutive days, animals received bilateral micro-injections of either vehicle or propranolol (4 µg in 1 µl/side) into the BLA (5 min before foot-shock stress). Behavioral (memory, as well as anxiety-like behaviors), electrophysiological, and histological (neural arborization in the hippocampal CA1 pyramidal neurons) studies were performed. Results showed that inhibition of ß-adrenoceptors of BLA by propranolol significantly further impaired fear and spatial memory in stressed rats. Similarly, propranolol effectively impaired both memories in the intact animals. Propranolol significantly amplified the slope and amplitude of fEPSP in the CA1 area of the hippocampus only in stressed rats. Foot-shock stress significantly increased the number of dendritic branches in the hippocampus, and propranolol suppressed this effect of stress. It is suggested that ß-adrenoceptors in the BLA promote memory and reduce anxiety-like behaviors under tonic and stress conditions. Propranolol dysregulated LTP parameters and reduced dendritic branches, resulting in memory impairment. Probably ß-adrenoceptors of BLA regulate evoked responses of CA1 neurons only in stress- and not the tonic condition.


Assuntos
Complexo Nuclear Basolateral da Amígdala , Propranolol , Animais , Medo/fisiologia , Masculino , Propranolol/farmacologia , Células Piramidais , Ratos , Ratos Wistar , Memória Espacial
15.
J Complement Integr Med ; 18(4): 701-710, 2021 May 10.
Artigo em Inglês | MEDLINE | ID: mdl-33962501

RESUMO

OBJECTIVES: Resveratrol as a natural polyphenolic agent can alleviate neuropathic pain symptoms. The mechanism of analgesic activity of resveratrol is far from clear. The current study examine whether analgesic activity of resveratrol is mediated by its neuroprotective and anti-oxidant activity in the neuropathic pain. We further examine whether analgesic activity of resveratrol is mediated by ß-adrenoceptors in the brain. METHODS: Neuropathic pain induced by L5 spinal nerve ligation (SNL). Male Wistar rats assigned into sham, SNL, SNL + resveratrol (40 µg/5 µL), and SNL + resveratrol + propranolol (a non-selective ß-adrenoceptor antagonist, 30 µg/5 µL) groups. Drugs injected intracerebroventricular (ICV) at day SNL surgery and daily for 6 days following SNL. Thermal allodynia and anxiety examined on days of -1, 2, 4, and 6 following SNL. Electrophysiological study performed on day 6 following SNL for evaluation of resveratrol effects on sciatic nerve conduction velocity (NCV). The activity of catalase (Cat) and superoxide dismutase (SOD) enzymes in the brain assessed on days 6 following SNL. RESULTS: Resveratrol significantly decreased thermal allodynia (and not anxiety) in all experimental days. Additionally, resveratrol significantly increased NCV, and also normalized the disrupted Cat and SOD activities following neuropathic pain. Furthermore, propranolol significantly blocked the analgesic and neuroprotective effects of resveratrol. CONCLUSIONS: It is suggested that the analgesic effects of resveratrol is mediated by its neuroprotective and antioxidant activities in the neuropathic rats. Furthermore, propranolol blocked the analgesic and neuroprotective effects of resveratrol.


Assuntos
Fármacos Neuroprotetores , Analgésicos/farmacologia , Analgésicos/uso terapêutico , Animais , Modelos Animais de Doenças , Hiperalgesia/tratamento farmacológico , Ligadura , Masculino , Fármacos Neuroprotetores/farmacologia , Fármacos Neuroprotetores/uso terapêutico , Propranolol/farmacologia , Ratos , Ratos Sprague-Dawley , Ratos Wistar , Resveratrol , Nervos Espinhais
16.
J Complement Integr Med ; 18(4): 711-717, 2021 May 12.
Artigo em Inglês | MEDLINE | ID: mdl-33979902

RESUMO

OBJECTIVES: We investigated effect of the ventromedial hypothalamus (VMH) dopamine D2 receptor inhibition on food intake and plasma ghrelin following chronic free or scheduled meal with different caloric intakes. METHODS: Male Wistar rats (220-250 g) were fed diets containing free (control) or three scheduled diets of standard, restricted and high-fat for 1 month. The animals stereotaxically received an intra VMH single dose of sulpiride (0.005 µg)/or saline (0.5 µL) before meal time. Thirty minutes later, food intake and circulating ghrelin were measured. RESULTS: Sulpiride significantly reduced food intake and ghrelin concentration in freely fed and scheduled-standard diet (p<0.05), while increased food intake, with ghrelin level on fasted level in scheduled-restricted group (p<0.01) compared to control. Food intake and ghrelin concentration between scheduled-high fat and freely fed or scheduled-standard diets did not show significant changes. CONCLUSIONS: The VMH D2 receptors are possibly involved in controlling scheduled eating behavior, depending on energy balance context.


Assuntos
Antagonistas dos Receptores de Dopamina D2/farmacologia , Ingestão de Alimentos , Grelina , Hipotálamo/efeitos dos fármacos , Sulpirida/farmacologia , Animais , Grelina/sangue , Masculino , Ratos , Ratos Wistar , Receptores de Dopamina D2
17.
Biochem Mol Biol Educ ; 49(4): 509-517, 2021 07.
Artigo em Inglês | MEDLINE | ID: mdl-33847452

RESUMO

Western blot (WB) or immunoblot is a workhorse method. It is commonly used by biologists for study of different aspects of protein biomolecules. In addition, it has been widely used in disease diagnosis. Despite some limitations such as long time, different applications of WB have not been limited. In the present review, we have summarized scientific and clinical applications of WB. In addition, we described some new generation of WB techniques.


Assuntos
Western Blotting/métodos , Western Blotting/normas , Proteínas/análise , Proteínas/metabolismo , Pesquisa Translacional Biomédica , Humanos , Proteínas/isolamento & purificação
18.
Clin Exp Pharmacol Physiol ; 48(6): 877-889, 2021 06.
Artigo em Inglês | MEDLINE | ID: mdl-33686675

RESUMO

Anxiety, hippocampus synaptic plasticity deficit, as well as pro-inflammatory cytokines, are involved in Alzheimer's disease (AD). The present study is designed to evaluate the possible therapeutic effect of crocin on anxiety-like behaviours, hippocampal synaptic plasticity and neuronal shape, as well as pro-inflammatory cytokines in the hippocampus using in vivo amyloid-beta (Aß) models of AD. The Aß peptide (1-42) was bilaterally injected into the frontal-cortex. Five hours after the surgery, the rats were given intraperitoneal (IP) crocin (30 mg/kg) daily up to 12 days. Elevated plus maze results showed that crocin treatment after bilateral Aß injection significantly increased the percentage of spent time into open arms, frequency of entries, and percentage of entries into open arms as compared with the Aß group. In the open field test, the Aß+crocin group showed a higher percentage of spent time in the centre and frequency of entries into central zone as compare with the Aß treated animals. Administering crocin increased the number of soma, dendrites and axonal arbores in the CA1 neurons among the rats with Aß neurotoxicity. Cresyl violet (CV) staining showed that crocin increased the number of CV-positive cells in the CA1 region of the hippocampus compared with the Aß group. Silver-nitrate staining indicated that crocin reduced neurofibrillary tangle formation induced by Aß. Crocin treatment attenuated the expression of TNF-α and IL-1ß mRNA in the hippocampus compared with the Aß group. Our results suggest that crocin attenuated Aß-induced anxiety-like behaviours and neuronal damage, and synaptic plasticity loss in hippocampal CA1 neurons may via its anti-inflammatory effects.


Assuntos
Peptídeos beta-Amiloides , Carotenoides , Doença de Alzheimer , Animais , Hipocampo , Masculino , Transtornos da Memória , Neurônios , Fragmentos de Peptídeos , Ratos
19.
Inflamm Res ; 70(4): 389-405, 2021 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-33608746

RESUMO

OBJECTIVE: Coronavirus disease 2019 (COVID-19) is a world-wide pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). To date, treatment of severe COVID-19 is far from clear. Therefore, it is urgent to develop an effective option for the treatment of patients with COVID-19. Most patients with severe COVID-19 exhibit markedly increased serum levels of pro-inflammatory cytokines, including interferon (IFN)-α, IFN-γ, and interleukin (IL)-1ß. Immunotherapeutic strategies have an important role in the suppression of cytokine storm and respiratory failure in patients with COVID-19. METHODS: A systematic search in the literature was performed in PubMed, Scopus, Embase, Cochrane Library, Web of Science, as well as Google Scholar preprint database using all available MeSH terms for Coronavirus, SARS-CoV-2, anti-rheumatoid agents, COVID-19, cytokine storm, immunotherapeutic drugs, IFN, interleukin, JAK/STAT inhibitors, MCP, MIP, TNF. RESULTS: Here, we first review common complications of COVID-19 patients, particularly neurological symptoms. We next explain host immune responses against COVID-19 particles. Finally, we summarize the existing experimental and clinical immunotherapeutic strategies, particularly anti-rheumatoid agents and also plasma (with a high level of gamma globulin) therapy for severe COVID-19 patients. We discuss both their therapeutic effects and side effects that should be taken into consideration for their clinical application. CONCLUSION: It is suggested that immunosuppressants, such as anti-rheumatoid drugs, could be considered as a potential approach for the treatment of cytokine storm in severe cases of COVID-19. One possible limitation of immunosuppressant therapy is their inhibitory effects on host anti-viral immune response. So, the appropriate timing of administration should be carefully considered.


Assuntos
COVID-19/epidemiologia , COVID-19/terapia , Síndrome da Liberação de Citocina/tratamento farmacológico , Fatores Imunológicos/uso terapêutico , Animais , Antirreumáticos/uso terapêutico , COVID-19/imunologia , Citocinas/metabolismo , Inibidores Enzimáticos/uso terapêutico , Humanos , Imunização Passiva , Imunossupressores/uso terapêutico , Imunoterapia , Inflamação/tratamento farmacológico , Interferons/uso terapêutico , Interleucina-1/antagonistas & inibidores , Interleucina-6/antagonistas & inibidores , Janus Quinase 1/antagonistas & inibidores , Espécies Reativas de Oxigênio/metabolismo , Insuficiência Respiratória/terapia , Fator de Transcrição STAT1/antagonistas & inibidores , Transdução de Sinais , Soroterapia para COVID-19
20.
Basic Clin Neurosci ; 12(5): 651-666, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-35173919

RESUMO

INTRODUCTION: The modality of γ-aminobutyric acid type a receptors (GABAA) controls dorsal horn neuronal excitability and inhibits sensory information. This study aimed to investigate the expression of the GABAA receptor and the effects of its agonist muscimol on Wide Dynamic Range (WDR) neuronal activity in the Chronic Constriction Injury (CCI) model of neuropathic pain. METHODS: Adult male Wistar rats weighing 200 to 250 g were used to induce CCI neuropathy. Fourteen days after surgery, muscimol (0.5, 1, and 2 mg/kg IP) was injected. Then, the behavioral tests were performed. After that, the animals were killed, and the lumbar segments of the spinal cords were collected for Western blot analysis of the GABAA receptor α1 subunit expression. The electrophysiological properties of WDR neurons were studied by single-unit recordings in separate groups 14 days after CCI. RESULTS: The outcomes indicated the development of thermal hyperalgesia and mechanical allodynia after neuropathy; nonetheless, the expression of the GABAA receptor α1 subunit did not change significantly. Moreover, the evoked responses of the WDR neurons to electrical, mechanical, and thermal stimuli increased considerably. Fourteen days after CCI, muscimol administration decreased thermal hyperalgesia, mechanical allodynia, and hyper-responsiveness of the WDR neurons in CCI rats. CONCLUSION: The modulation of the spinal GABAA receptors after nerve injury can offer further insights to design new therapeutic agents to reduce neuropathic pain symptoms.

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