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1.
J Physiol Pharmacol ; 67(3): 465-9, 2016 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-27512007

RESUMO

The present study investigates the effects of pregabalin (PGB) and codeine (COD) combination on neuropathic hyperalgesia in an animal model of peripheral nerve injury represented by partial sciatic nerve ligation. Hot plate and analgesimeter tests were performed to evaluate the influence of PGB, COD and their combination on thermal and mechanical hyperalgesia in the hind paw with partial sciatic nerve ligation. Reactivity was evaluated by measuring the latency to withdrawal of the operated hind paw from the noxious heat and pressure stimulation. Nociceptive thresholds were evaluated before (baseline) and in the 1(st), 3(rd), 5(th) and 7(th) day after surgical procedure. The investigation demonstrates that the treatment with PGB attenuated partial sciatic nerve ligation development of thermal and mechanical hyperalgesia in rats operated hind paw. The oral administration, during 14 consecutive days of PGB-COD combination significantly reduced the degree of both thermal and mechanical hyperalgesia in the hind paw with partial sciatic nerve ligation. These results suggest that the association of PGB with COD exerted ameliorative effect on partial sciatic nerve ligation-induced neuropathic pain in rats.


Assuntos
Analgésicos/uso terapêutico , Codeína/uso terapêutico , Hiperalgesia/tratamento farmacológico , Mononeuropatias/tratamento farmacológico , Neuralgia/tratamento farmacológico , Pregabalina/uso terapêutico , Animais , Combinação de Medicamentos , Temperatura Alta/efeitos adversos , Ligadura , Masculino , Estimulação Física/efeitos adversos , Ratos Wistar , Nervo Isquiático/cirurgia
2.
Rev Med Chir Soc Med Nat Iasi ; 120(4): 942-6, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-30141891

RESUMO

Nitric oxide (NO), formerly known as the endothelium-derived relaxing factor, is a mediator with a key role in the body, both in the central nervous system and in periphery. NO is synthesized by several cell types, where it acts as an autocrine and paracrine signaling molecule. Harnessing the impressive therapeutic potential of nitric oxide (NO) remains an ongoing challenge. In order to overcome the limitations linked with the use of nitric oxide and specially to increase the release of the radical in the targeted area, promising therapeutic strategies have been implemented, based on specific technologies which create releasing agents and vehicles for nitric oxide. Organic nitrites are the most known NO donor drugs, used especially in the treatment of cardiovascular diseases. In recent years, technological advances have allowed obtaining variations synthetic derivatives (such as diazeniumdiolates, S-nitrosothiols), which can generate NO in a controlled mode in the body and to chemically stabilize it; these compounds were studied with promising results in various animal models of vasospasm and pulmonary hypertension. Another high value therapeutic path is represented by the development of hybrid drugs (new nonsteroidal anti-inflammatory NO donor agents), with practical applications in inflammatory disorders accompanied by pain. Also, there is increasing evidence of the existence of NO donors with important antioxidant and hepatoprotective effects.


Assuntos
Anti-Inflamatórios não Esteroides/uso terapêutico , Doenças Cardiovasculares/tratamento farmacológico , Doadores de Óxido Nítrico/uso terapêutico , Óxido Nítrico/metabolismo , Animais , Desenho de Fármacos , Medicina Baseada em Evidências , Humanos , Hipertensão Pulmonar/tratamento farmacológico , Doadores de Óxido Nítrico/química , Resultado do Tratamento
3.
Rev Med Chir Soc Med Nat Iasi ; 119(1): 193-200, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25970966

RESUMO

UNLABELLED: Discovered in 1984, imidazoline receptors (I1, I2, I3) are located centrally and peripherally being involved in various physiologic and pathophysiologic processes in the body. Experimental and clinical investigations have suggested the interrelations between imidazoline, adrenergic, dopaminergic, glutamatergic and opioid systems, which may explain the influence of different substances acting on imidazoline receptors in cognitive disorders, behavioral disturbances and motor diseases pathways. AIM: To investigate the effects of two imidazoline receptor antagonists on locomotor activity and endurance capacity in rats. MATERIAL AND METHODS: The experiment was carried out with white male Wistar rats (200-250 g) divided into 3 groups of 7 animals each, treated intraperitonealy with the same volume of solution as follows: Group I (Control): distilled water 0.3 ml/100 g body weight; Group II (IDZ): idazoxan 3 mg/kbw; Group III (EFR): efaroxan 1 mg/kbw. Exercise capacity was evaluated using a locomotor PanLAB treadmill test. The data were presented as mean +/- standard deviation and significance was tested by SPSS Statistics for Windows version 17.0 and ANOVA method. Experimental protocol was implemented according to recommendations of the Gr.T. Popa" University Committee for Research and Ethical Issues. RESULTS: Intraperitoneal administration of idazoxan and efarox- an resulted in a significant increase in running distance compared with the control group (p < 0.05). At the same time a reduction in the number and time of electric shocks delivered to motivate the animal to keep running was observed. In this experimental behavioral model the effects of idazoxan on the evaluated parameters were more intense than those of efaroxan. CONCLUSIONS: In our experimental conditions we demonstrated the ability of imidazoline receptor antagonists idazoxan and efaroxan to improve fatigue resistance during forced running in rats.


Assuntos
Antagonistas Adrenérgicos alfa/farmacologia , Benzofuranos/farmacologia , Idazoxano/farmacologia , Imidazóis/farmacologia , Movimento/efeitos dos fármacos , Animais , Modelos Animais de Doenças , Teste de Esforço , Injeções Intraperitoneais , Masculino , Ratos , Ratos Wistar
4.
Rev Med Chir Soc Med Nat Iasi ; 118(3): 847-53, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25341311

RESUMO

AIM: The study investigates the effects of magnesium nanovesicles on the memory processes performance in mice. MATERIALS AND METHODS: L-a-phosphatidylcholine was used to obtain nano formulations as lipid vesicles systems stabilized thereafter with chitosan. The experiment was carried out on white Swiss mice, divided into 3 groups of 7 animals each, treated orally 7 consecutive days: Group I (Control): 0.1 mL/10g distilled water; Group II (Mg): 1 mmol/kbw magnesium chloride; Group III (Mg-vesicles): 1 mmol/kbw magnesium nanovesicles. The spatial memory performance was assessed by recording spontaneous alternation behavior in Y-maze test. Each animal was placed at the end of one arm and allowed to move freely through the maze during a single 8 min session. Alternation was defined as a consecutive entry in three different arms. The alternation percentage was computed according to the formula: (number of alternations/total number of arm visits--2) x 100. Data were analyzed using SPSS 17.0 software. Experimental protocols were implemented according to the recommendations of the University Committee for Research and Ethical Issues. RESULTS: New carrier formulations entrapping magnesium chloride were designed: their mean size was 129.56 nm and the mean Zeta potential was +36.1 mV, indicating a moderate stability of the solution. Oral administration of magnesium vesicles resulted in a significant increase of spontaneous alternation percent in Y-maze test (p < 0.01), which suggests an improvement of short-term memory. CONCLUSIONS: Using magnesium chloride entrapped in lipid vesicles induced an enhancement of cognitive functions in mice especially by facilitation of learning extinction.


Assuntos
Magnésio/farmacologia , Aprendizagem em Labirinto/efeitos dos fármacos , Memória/efeitos dos fármacos , Animais , Modelos Animais de Doenças , Cloreto de Magnésio/farmacologia , Memória de Curto Prazo/efeitos dos fármacos , Camundongos , Nanocápsulas , Percepção Espacial
5.
Rev Med Chir Soc Med Nat Iasi ; 118(3): 854-9, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25341312

RESUMO

AIM: To investigate the effects of two serotonin receptor antagonists on spontaneous behavior in rats. MATERIAL AND METHOD: The experiment was carried out on white male Wistar rats (150-200g) divided into 3 groups of 6 animals each, treated intraperitoneally with the same volume of solution as follows: Group I (Control): saline solution 0.1 ml/10 g weight; Group II (SB-269970): SB-269970 1 mg/kbw; Group III (NAN-190): NAN-190 1 mg/kbw. The effects of serotonin receptor antagonists on the spontaneous psychomotor skills of rats were tested in Actimeter LE-8811 (PanLab). The data were presented as mean +/- standard deviation and significance was tested by SPSS Statistics for Windows version 17.0 and ANOVA method. The experimental protocol was implemented according to the guidelines for handling and use of experimental animals of the Research Ethics Committee of the Iasi "Grigore T. Popa" University and ethical standards of the European Community. RESULTS: The 5HT1 serotonin receptor antagonist NAN-190 determined a statistically significant reduction (p < 0.01) in both horizontal and vertical movements as compared with the control group, whereas the 5HT7 serotonin receptor antagonist SB269970 had no influence on rat behavioral manifestations. CONCLUSIONS: In our experimental conditions 1 mg/kbw NAN-190 decreased the total escape attempts, corresponding to a significant diminution of exploratory and self-maintenance spontaneous behavior in this experimental animal model. These manifestations may be correlated with the anxiolytic effect of 5HT1 serotonin receptor antagonist NAN-190 in rats. The administration of 5HT7 serotonin receptor antagonist SB-269970 did not alter the spontaneous activity in this behavioral experimental model in rats.


Assuntos
Ansiolíticos/farmacologia , Movimento/efeitos dos fármacos , Fenóis/farmacologia , Antagonistas da Serotonina/farmacologia , Sulfonamidas/farmacologia , Animais , Modelos Animais de Doenças , Masculino , Ratos , Ratos Wistar , Antagonistas do Receptor 5-HT1 de Serotonina/farmacologia
6.
Rev Med Chir Soc Med Nat Iasi ; 114(2): 510-4, 2010.
Artigo em Romano | MEDLINE | ID: mdl-20700994

RESUMO

AIM: To evaluate immune system response, skin and hepatic reactivity in Swiss mice after retro auricular local administration of two textile dyes. MATERIAL AND METHODS: On 3 groups of white Swiss mice: group I (Cibacron Yellow F-4G), group II (Cibacron Orange P-2R) and control group (DMSO dimethylsulfoxide), substances were applied on left retro auricular ear, in dose of 25 microL solution 10% in DMSO (the dyes were not soluble in water), once a day, for 7 days. After euthanasia, blood samples were taken to assay differential cell count, peripheral neutrophils activity (NBT test), serum opsonic capacity, peritoneal macrophages activity (phagocytic and bactericidal capacity), and activity of spleenic T-lymphocytes with rossetting capacity, and spleen cells forming Jerne plaques. There were taken skin from local application of dyes, retro auricular and later cervical nodes from left side and hepatic samples. RESULTS: Retro auricular and later cervical nodes mass increases after administration of textile dyes, compared to control group. Basophiles percentages were increased after administration of two dyes (stronger after yellow dye). Peripheral neutrophils activity was increased after administration of two dyes, especially after orange dye. Administration of the two dyes decreased serum opsonic capacity and peritoneal macrophages activity, but did not influenced the activity of spleenic T-lymphocytes with rossetting capacity and spleen cells forming Jerne plaques. There were significant skin and hepatic changes in microscopy. CONCLUSION: The studied dyes influenced the activity of immune system, increased skin and hepatic reactivity.


Assuntos
Corantes/toxicidade , Orelha Externa , Fígado/efeitos dos fármacos , Fígado/imunologia , Pele/efeitos dos fármacos , Pele/imunologia , Indústria Têxtil , Administração Cutânea , Animais , Compostos Azo/toxicidade , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Fatores Imunológicos/imunologia , Ensaio Local de Linfonodo , Macrófagos Peritoneais/efeitos dos fármacos , Macrófagos Peritoneais/imunologia , Camundongos , Neutrófilos/efeitos dos fármacos , Neutrófilos/imunologia , Proteínas Opsonizantes/imunologia , Fagócitos/efeitos dos fármacos , Fagócitos/imunologia , Baço/citologia , Baço/efeitos dos fármacos , Linfócitos T/efeitos dos fármacos , Linfócitos T/imunologia , Triazinas/toxicidade
7.
Rev Med Chir Soc Med Nat Iasi ; 114(1): 277-81, 2010.
Artigo em Romano | MEDLINE | ID: mdl-20509316

RESUMO

UNLABELLED: Reactive Red 183, Reactive Red 2 and Reactive Blue 204 (red dye, green dye and blue dye) are three reactive dyes frequently used in textile industry. In some atmospheric conditions ( high temperature, perspiration, pH values, UV/IR radiations), some quantities of these hydrolyzed dyes, could pass from textile clothes directly into the human skin. MATERIAL AND METHOD: There were used 4 groups of white Swiss mice (with similar weight and number of both sexes), control group and 3 groups, treated once daily with a retro-auricular application of different reactive dyes. After 14 days of treatment, blood samples were taken from retro-orbitary plexus to assess leukocyte count, phagocytic capacity of peripheral neutrophils, serum opsonic capacity, phagocyte capacity and bactericidal capacity of peritoneal macrophages, splenic T lymphocytes with rossetting capacity and spleen cells forming Jerne plaques. The retro-acuricular and latero-cervical nodes were weighted. RESULTS: Red dye did not influence the weight of the studied nodes, but determined statistically significant modifications on non-specific immune system parameters. Blue and grena dyes determined modifications of weight especially of retroauricular nodes. Grena dye determined important effects of non-specific immune system parameters (serum opsonic capacity, phagocyte capacity and bactericidal capacity of peritoneal macrophages). The blue dye did not determine a biological response. CONCLUSION: Red and green dye determined important effects on non-specific immune system parameters.


Assuntos
Corantes/toxicidade , Fatores Imunológicos/imunologia , Proteínas Opsonizantes/imunologia , Pele/imunologia , Linfócitos T/imunologia , Indústria Têxtil , Administração Cutânea , Animais , Biomarcadores/sangue , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Leucócitos/imunologia , Macrófagos/imunologia , Camundongos , Fagócitos/imunologia , Têxteis
8.
Rev Med Chir Soc Med Nat Iasi ; 112(4): 1092-7, 2008.
Artigo em Romano | MEDLINE | ID: mdl-20209793

RESUMO

UNLABELLED: The effects of the saponinic summ extracted from roots of Aralia mandshurica have been studied in experimentally animals exposed to stress. MATERIAL AND METHODS: The experiment was carried out on 4 groups of animals divided into 24 lots of 12 white rats each with experimentally induced chronic inflammation or/and exposed to stress induced by exposure to continuous dark or light. The drugs (Levamisole (LVM) (10mg/kg bw/day), Indometacin (IND) (1.42 mg/kg bw/day), Extract of the roots of Aralia mandshurica (SAR) (26.25 mg/kg bw/day) and saline solution (0.5 mL/100 g bw/day) were administered orally for 14 days, in unique daily dose. Blood samples were taken from rats' retroorbital plexus before the beginning of the treatment protocol (M0) and at the finish of the treatment (M1) in order to assay differential cell count, peripheral neutrophils activity (NBT test) and serum complement activity. RESULTS: The SAR extracts exert influence on immunity defence cellular's components without influence on humoral efects, no matter of experimentally conditions. They determined decreasing of the percentage of the neutrophils in peripheral blood (at the lower levels than Indometacin (IND). CONCLUSION: The experimental results demonstrated immunomodulatory effect of this saponine extract.


Assuntos
Ansiolíticos/uso terapêutico , Aralia , Fitoterapia/métodos , Extratos Vegetais/uso terapêutico , Raízes de Plantas , Estresse Fisiológico/efeitos dos fármacos , Animais , Ansiolíticos/farmacologia , Modelos Animais de Doenças , Extratos Vegetais/farmacologia , Ratos , Ratos Wistar , Romênia
9.
Ann Pharm Fr ; 62(1): 43-8, 2004 Jan.
Artigo em Francês | MEDLINE | ID: mdl-14747772

RESUMO

An original phenothiazine, CPTZ, was tested for its effects on the mouse immune system. Serum opsonic capacity, phagocyte and bactericidal activity of peritoneal macrophages, counts of splenic cells forming hemolysis plaques, and the number of survivors after experimental infection were recorded. The effects observed were compared with those produced by levamisole (a non-selective immunomodulator) and indometacin (an antiinflammatory drug with selective immunomodulator properties). The effects of CPTZ might be useful for the development of a new class of immunosuppressor drugs.


Assuntos
Imunossupressores/síntese química , Imunossupressores/farmacologia , Fenotiazinas/síntese química , Fenotiazinas/farmacologia , Adjuvantes Imunológicos/farmacologia , Animais , Feminino , Indometacina/farmacologia , Levamisol/farmacologia , Macrófagos Peritoneais/efeitos dos fármacos , Macrófagos Peritoneais/imunologia , Masculino , Camundongos , Proteínas Opsonizantes/sangue , Fagocitose/efeitos dos fármacos , Linfócitos T/efeitos dos fármacos , Linfócitos T/imunologia
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