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1.
J Neuroendocrinol ; 30(4): e12592, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29543349

RESUMO

Both serotonin (5-HT) and stress exert changes in cortical inhibitory tone to shape the activity of cortical networks. Because astrocytes are also known to affect inhibition through established purinergic pathways, we assessed the role of GABA and purinergic pathways with respect to the effects of rapid corticosterone (CORT) and 5-HT on cortical inhibition. We used a paired-pulse paradigm (P1 and P2) in acutely isolated mouse brain slices to evaluate changes in cortical evoked inhibition. Normally, 5-HT decreases the amplitude of the first pulse P1, whereas it increases the amplitude of P2 (increasing frequency transmission). Interestingly, it was observed that CORT application decreased P1 and increased P2 similar to that of 5-HT application. Given that CORT and 5-HT are known to modulate inhibition, we applied the GABAA antagonist bicuculline in the presence of both and found that the increase in P2 and the P2/P1 was lost, providing evidence for a common mechanism involving GABAA receptor signalling. Additional occlusion experiments (ie, 5-HT in presence of CORT and CORT in presence of 5-HT) provide further support for a common mechanism. Because both 5-HT and CORT blocked the increase in P2 and P2/P1 with respect to the other, we suggest 5-HT/CORT already utilise the shared mechanism to affect cortical inhibition. Using low concentrations of the GAPDH inhibitor iodoacetate, as commonly used to selectively disrupt astrocyte metabolism, we found that the increase in P2 and P2/P1 was similarly blocked in response to both CORT and 5-HT. Because astrocyte signalling depends in large part on purinergic pathways, the purinergic contribution was assessed using Ab129 (P2Y antagonist) and SCH 58261 (A2A antagonist). Once again, P2Y and A2A receptor blockade similarly disrupted 5-HT- or CORT-mediated increases in P2 and P2/P1. Taken together, these results support the common involvement of GABAergic and purinergic pathways in the effects of CORT and 5-HT that may also involve astrocytes.


Assuntos
Encéfalo/efeitos dos fármacos , Corticosterona/farmacologia , Potenciais Pós-Sinápticos Inibidores/efeitos dos fármacos , Neurônios/efeitos dos fármacos , Serotonina/farmacologia , Animais , Astrócitos/efeitos dos fármacos , Bicuculina/farmacologia , Potenciais Pós-Sinápticos Excitadores/efeitos dos fármacos , Antagonistas de Receptores de GABA-A/farmacologia , Masculino , Camundongos , Inibição Neural/efeitos dos fármacos , Vias Neurais/efeitos dos fármacos , Transdução de Sinais/efeitos dos fármacos , Transdução de Sinais/fisiologia
2.
J Dev Orig Health Dis ; 6(6): 501-11, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26279187

RESUMO

Innate-like B1a lymphocytes arise from long-lived progenitors produced exclusively by fetal stem cells. Any insults coinciding with this early lymphopoietic wave could have a permanent impact on the B1a population and its unique protein products, the natural antibodies (NAb). We investigated early life nutritional influences on NAb concentrations of pre-adolescent children (n=290) in rural Nepal for whom we had extensive information on exposures from pregnancy and early infancy. Infant size and growth were strongly associated with NAb concentrations at 9-13 years of age among males (e.g., for neonatal weight: ßBOYS=0.43; P<0.001), but not females (e.g., for neonatal weight: ßGIRLS=-0.16; P=0.26). In females, season of birth was associated with NAb concentrations, with marked reductions among girls born during the pre-monsoon (March-May; ßGIRLS=-0.39; P=0.01) and pre-harvest (September-November; ßGIRLS=-0.35; P=0.03) seasons. Our findings suggest that nutritional or other environmental influences on immune development may vary by sex, with potential consequences for immune function during infancy and long-term risk of immune-mediated disease.


Assuntos
Anticorpos/sangue , Linfócitos B/fisiologia , Efeitos Tardios da Exposição Pré-Natal/epidemiologia , Criança , Desenvolvimento Infantil , Estudos Transversais , Feminino , Humanos , Imunidade Humoral , Lactente , Masculino , Nepal/epidemiologia , Estado Nutricional , Gravidez , Fenômenos Fisiológicos da Nutrição Pré-Natal , Fatores Sexuais
4.
Vet Pathol ; 46(6): 1258-69, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19605900

RESUMO

Leukoencephalomyelopathy of undetermined etiology has been described in specific pathogen-free cats. A study was established to assess if the long-term feeding of a gamma-irradiated diet could induce this disease. Cats fed exclusively on diet irradiated at 25.7-38.1 kGy ("typical" dose) and 38.1-53.6 kGy (high-end dose), respectively, developed typical lesions with attendant, progressively severe ataxia between study days 140 and 174. The onset of ataxia at day 140 and the number of animals affected at this time were similar in animals fed each ration. A maximum ataxia "score" was first reached by an animal on the high-end dose diet on day 167 and by 2 cats fed the "typical-end" dose diet 21 days later. Ataxic cats and 1 animal euthanized on day 93 prior to the onset of ataxia exhibited varying degrees of Wallerian degeneration in the spinal cord and brain, similar to the spontaneous disease. The elevated total antioxidant status of spinal cord segments and hepatic superoxide dismutase concentration of cats fed typical and high-end treated diets suggested free-radical involvement in the pathogenesis. The significantly elevated peroxide concentrations of the irradiated diets (1,040% and 6,440% of untreated values) may have resulted in increased oxidative insult, a factor possibly exacerbated by the treated diets' reduced vitamin A content. This study has reproduced leukoencephalomyelopathy in cats similar to spontaneous outbreaks by feeding a gamma-irradiated dry diet with elevated peroxide and reduced vitamin A concentrations.


Assuntos
Ração Animal/efeitos da radiação , Doenças do Gato/patologia , Dieta/veterinária , Raios gama , Leucoencefalopatias/veterinária , Ração Animal/efeitos adversos , Ração Animal/análise , Fenômenos Fisiológicos da Nutrição Animal , Animais , Deficiência de Vitaminas/induzido quimicamente , Gatos , Gorduras na Dieta , Proteínas Alimentares , Análise de Alimentos , Leucoencefalopatias/patologia , Fígado/metabolismo , Fígado/patologia , Masculino , Organismos Livres de Patógenos Específicos , Medula Espinal/metabolismo , Medula Espinal/patologia , Vitaminas/análise , Degeneração Walleriana/patologia , Degeneração Walleriana/veterinária
6.
Vet Pathol ; 44(6): 912-6, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18039904

RESUMO

Investigations were carried out on 8 specific pathogen-free cats (5 male and 3 female) from a colony experiencing "outbreaks" of progressive hind limb ataxia in 190 of 540 at-risk animals ranging from 3 months to 3 years old. These studies identified moderate to severe bilateral axonal degeneration within white matter regions of the cervical, thoracic, and lumbar spinal cord and in the white matter of the cerebral internal capsule and peduncle, in the roof of the fourth ventricle and inferior cerebellar peduncle, and in the external arcuate and pyramidal fibres of the medulla. There were varying degrees of accompanying microgliosis, astrocytosis, and capillary hyperplasia. Such a clinicopathologic syndrome, termed feline leukoencephalomyelopathy, has previously been described in cat colonies in Britain and New Zealand, although its etiology has not been determined. The degenerative nature of the lesions and their bilateral distribution suggest possible nutritional, metabolic, or toxic causes. Although these findings provide circumstantial evidence that the exclusive feeding of a gamma-irradiated diet of reduced vitamin A content is associated with the development of the neuronal lesions, further tissue micronutrient and antioxidant analysis will be required to support this hypothesis.


Assuntos
Encefalopatias/veterinária , Doenças do Gato/patologia , Doenças da Medula Espinal/veterinária , Animais , Encefalopatias/patologia , Gatos , Feminino , Masculino , Organismos Livres de Patógenos Específicos , Medula Espinal/patologia , Doenças da Medula Espinal/patologia
7.
Vet Pathol ; 44(6): 949-51, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18039912

RESUMO

A Siamese kitten presented with mild gait dysfunction associated with periodic circling. Pathologic investigation revealed unilateral (right-sided) absence of the corticospinal (pyramidal) tract throughout its normal course. Although an infectious cause cannot be completely ruled out a genetic etiology was suspected.


Assuntos
Doenças do Gato/patologia , Tratos Piramidais/patologia , Doenças da Medula Espinal/veterinária , Animais , Doenças do Gato/congênito , Gatos , Feminino , Doenças da Medula Espinal/congênito , Doenças da Medula Espinal/patologia
8.
J Small Anim Pract ; 48(1): 49-52, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17212751

RESUMO

An unusual case of unilateral trigeminal neuronopathy in a dog is reported, in which the motor nucleus of the trigeminal nerve and the ipsilateral corticospinal tract were destroyed, apparently by a cerebrovascular accident (stroke). Hemiplegia did not occur. Neuropathological changes are described, including remyelination by Schwann cells in the central nervous system. The case illustrates the importance of central nervous system post-mortem examination when establishing causes of cranial nerve paralysis.


Assuntos
Infarto Cerebral/veterinária , Doenças do Cão/patologia , Neurônios Motores/patologia , Ponte , Núcleo Espinal do Trigêmeo/patologia , Animais , Infarto Cerebral/patologia , Cães , Eutanásia Animal , Masculino , Núcleo Espinal do Trigêmeo/lesões
9.
Biochem J ; 358(Pt 3): 737-45, 2001 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-11535134

RESUMO

Chemokines interact with specific G-protein-coupled cell-surface receptors and with glycosaminoglycans (GAGs), such as heparan sulphate. Although chemokines often form multimers in solution, this process may be enhanced following interaction with GAGs on the cell surface, or within the extracellular matrix. However, the significance of multimerization for chemokine function remains controversial. In the present study, a fusion protein was prepared between the prototypical human CC chemokine, monocyte chemoattractant protein-1 (MCP-1; also known as CCL-2) and a large secreted placental alkaline phosphatase (SEAP) moiety. This fusion protein (MCP-1-SEAP) remained monomeric under conditions that promote oligomerization of the native chemokine. Radioligand binding showed that both native MCP-1 and MCP-1-SEAP competed for the same site on the surface of HEK-293 cells expressing the CCR2b chemokine receptor. The interaction between either chemokine species and endothelial cell surface GAGs was antagonized by the addition of the heparan sulphate-like molecule, heparin. Both MCP-1 and MCP-1-SEAP induced a Ca(2+)-flux in the THP-1 monocytic cell line, and were equally effective at promoting transendothelial chemotaxis of mononuclear immune cells, with maximal migration being produced by treatment with 12 nM of either species. In each case this chemotactic response was almost completely antagonized by the addition of heparin. The importance of interaction between either native MCP-1 or MCP-1-SEAP and cell-surface GAGs for transcellular migration was demonstrated by the almost complete absence of leucocyte chemotaxis across monolayers of GAG-deficient mutant cells. In summary, this study shows that multimerization is neither necessary for, nor potentiates, the biological activity of MCP-1. However, the results do clearly demonstrate the importance of the interaction between MCP-1 and cell-surface heparan sulphate for transmonolayer leucocyte chemotaxis.


Assuntos
Quimiocina CCL2/fisiologia , Quimiotaxia de Leucócito , Endotélio Vascular/fisiologia , Glicosaminoglicanos/farmacologia , Monócitos/fisiologia , Receptores de Quimiocinas/fisiologia , Células 3T3 , Fosfatase Alcalina/genética , Fosfatase Alcalina/metabolismo , Animais , Sítios de Ligação , Células CHO , Cálcio/metabolismo , Linhagem Celular , Membrana Celular/fisiologia , Células Cultivadas , Quimiocina CCL2/genética , Quimiocina CCL2/farmacologia , Quimiotaxia de Leucócito/efeitos dos fármacos , Clonagem Molecular , Cricetinae , Endotélio Vascular/citologia , Feminino , Heparina/farmacologia , Humanos , Ligantes , Substâncias Macromoleculares , Camundongos , N-Formilmetionina Leucil-Fenilalanina/farmacologia , Placenta/enzimologia , Gravidez , Receptores CCR2 , Receptores de Quimiocinas/genética , Proteínas Recombinantes de Fusão/metabolismo , Proteínas Recombinantes/metabolismo , Transfecção
10.
Vet Rec ; 149(2): 49-54, 2001 Jul 14.
Artigo em Inglês | MEDLINE | ID: mdl-11488342

RESUMO

Progressive ataxia, with head tremor, developed in 10 captive-born cheetah cubs under six months of age. The condition was usually preceded by coryza and an ocular discharge. Initially the ataxia and weakness affected the hindquarters, then the forelegs, and head tremor developed later. Significant pathological changes were confined to the central nervous system. There was widespread Wallerian degeneration in the funiculi of the spinal cord (except those in the dorsal columns), in the medulla and in the cerebellum. In the cerebellum there was degeneration of Purkinje cells and of the molecular and granular cell layers. There was chromatolysis in the Purkinje cells, the ventral horn cells of the spinal cord and in the neurons of the lateral vestibular nucleus. The olivary nucleus was necrotic. There were foci of inflammatory cells in the molecular layer of the cerebellum and in the medulla. The cause of the disease remains unknown.


Assuntos
Acinonyx , Ataxia/veterinária , Doenças do Sistema Nervoso Central/veterinária , Degeneração Walleriana/veterinária , Animais , Ataxia/etiologia , Ataxia/patologia , Doenças do Sistema Nervoso Central/etiologia , Doenças do Sistema Nervoso Central/patologia , Cerebelo/patologia , Córtex Cerebral/patologia , Feminino , Masculino , Microscopia Eletrônica/veterinária , Células de Purkinje/patologia , Medula Espinal/patologia , Degeneração Walleriana/etiologia , Degeneração Walleriana/patologia
11.
Vet Rec ; 148(18): 564-7, 2001 May 05.
Artigo em Inglês | MEDLINE | ID: mdl-11370881

RESUMO

A four-year-old wire-haired dachshund developed progressive neurological signs of ataxia, intention tremor and finally dysuria. Two years later, histopathology showed that neurons throughout the brain and spinal cord were distended with lipopigment which was also present in macrophages. Ultrastructurally, the pigment in the neurons occurred predominantly as electron-dense membranous whorls and stacks. There were a few vacuolated macrophages in the meninges. Hepatocytes were highly vacuolated and electron microscopy suggested that they were empty membrane-bound vesicles. The disease was diagnosed as mucopolysaccharidosis IIIA because of its similarity to other biochemically confirmed cases in the same breed and in a New Zealand huntaway dog. Additional lesions included calcium oxalate uroliths, severe secondary calcification of tissues including the brain and storage deposits in some neurons, and lesions which may have been associated with high levels of the substrate, heparan sulphate.


Assuntos
Ataxia/veterinária , Doenças do Cão/diagnóstico , Mucopolissacaridose III/veterinária , Animais , Ataxia/etiologia , Morte Súbita/veterinária , Diagnóstico Diferencial , Doenças do Cão/patologia , Cães , Masculino , Mucopolissacaridose III/complicações , Mucopolissacaridose III/diagnóstico , Neurônios/patologia , Neurônios/ultraestrutura
12.
Ann Emerg Med ; 36(6): 554-60, 2000 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11097694

RESUMO

STUDY OBJECTIVE: A rule based on presenting chief complaints can identify patients for a rapid (5-minute) ECG and decrease delays in treatment of patients with acute myocardial infarction (MI). METHODS: The presenting chief complaint was electronically collected on all patients treated in a community teaching hospital emergency department. A rule for ordering ECG on patient presentation to the ED was developed from a model set of patients presenting from July through December 1994 (22,717 patients) and then tested on a validation set of patients from January through May 1995 (18,759 patients). Outcome measures (delay in performance of ECG and delay in administration of thrombolytic agents) were prospectively collected on written data sheets before (April 1993-May 1995, n=67) and after (June 1995-March 1997, n=128) implementation of the rule at the study hospital. RESULTS: On the model set, 193 patients had the final diagnosis of MI, with 5 chief complaints having the best performance in identifying patients with acute MI and comprising the rapid ECG rule: older than 30 years with chest pain (130 [67.4%] patients); older than 50 years with syncope (5 [1%] patients); weakness (12 [6.2%] patients); rapid heart beat (2 [1%] patients); and difficulty breathing or shortness of breath (20 [10.4%] patients). On the validation set, 142 patients had the final diagnosis of MI, with the rule performing better than chest pain in identifying patients for a "stat" ECG (sensitivity 93.7% versus 67. 4% [95% confidence interval (CI) of the difference, 15.6% to 33.8%]), although a larger percentage of ED patients would receive a stat ECG (7.3% versus 6.3% [95% CI of the difference, 0.7% to 1.7%]). During the model and validation period, 44 (13.1%) of 335 patients with MI received thrombolytic agents. The rule had higher sensitivity on patients with MI treated with thrombolytic agents compared with patients with MI not treated with thrombolytic agents (sensitivity 100% versus 86.4% [95% CI of the difference, 1.7% to 20. 3%] and specificity of 90.4% versus 93.8% [95% CI of the difference, 3.0% to 3.8%]). For the 4-year study period, outcome improved after the implementation of the rule: mean delay in performing ECGs in patients with MI who were administered thrombolytic agents decreased from 10.0 to 6.3 minutes (95% CI of the difference, 1.1 to 6.4), and mean delay in administering thrombolytic agents decreased from 36.9 to 26.1 minutes (95% CI of the difference, 3.5 to 17.7). CONCLUSION: Use of a rule based on chief complaints can identify patients with MI for immediate ECG and decrease delays in performing ECGs and administration of thrombolytic agents.


Assuntos
Dor no Peito/diagnóstico , Eletrocardiografia/métodos , Infarto do Miocárdio/diagnóstico , Terapia Trombolítica/métodos , Triagem , Adulto , Idoso , Dor no Peito/fisiopatologia , Intervalos de Confiança , Serviço Hospitalar de Emergência , Tratamento de Emergência/métodos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Infarto do Miocárdio/tratamento farmacológico , Valor Preditivo dos Testes , Probabilidade , Estudos Prospectivos , Sensibilidade e Especificidade , Estatísticas não Paramétricas , Fatores de Tempo , Resultado do Tratamento
14.
J Biol Chem ; 275(16): 11721-7, 2000 Apr 21.
Artigo em Inglês | MEDLINE | ID: mdl-10766793

RESUMO

Chemokines are a group of small proteins that have a variety of functions, including the activation and recruitment of immune cells during episodes of inflammation. In common with many cytokines, it has been observed that chemokines have the potential to bind heparin-like glycosaminoglycan molecules, which are normally expressed on proteoglycan components of the cell surface and extracellular matrix. The significance of this interaction for chemokine activity remains a subject of debate. In this study, Chinese hamster ovary cells were transfected separately with the human chemokine receptors CCR1 and CCR5, and these receptors were shown to induce an intracytoplasmic Ca(2+) flux and cellular chemotaxis following stimulation with the natural CC chemokine ligands (MIP-1alpha, RANTES (regulated on activation normal T cell expressed), and MIP-1beta). In further experiments, mutant CHO cells, with a defect in normal glycosaminoglycan (GAG) expression, were also transfected with, and shown to express similar levels of, CCR1 and CCR5. Although these receptors were functional, it was found that the mutant cells required exposure to higher concentrations of ligands than the wild-type cells in order to produce the same intracytoplasmic Ca(2+) flux. Radioligand binding experiments demonstrated that specific chemokine receptors expressed by wild-type cells had a significantly greater affinity for MIP-1alpha than similar receptors expressed by GAG-deficient mutants. However, there was no significant difference between these cells in their affinity for RANTES or MIP-1beta. In conclusion, it has been demonstrated clearly that GAG expression is not necessary for the biological activity of the chemokines MIP-1alpha, RANTES, or MIP-1beta. However, the presence of cell surface GAGs does enhance the activity of low concentrations of these chemokines by a mechanism that appears to involve sequestration onto the cell surface.


Assuntos
Quimiocina CCL5/fisiologia , Glicosaminoglicanos/fisiologia , Heparina , Proteínas Inflamatórias de Macrófagos/fisiologia , Animais , Células CHO , Cálcio/metabolismo , Separação Celular , Quimiocina CCL3 , Quimiocina CCL4 , Cricetinae , Citometria de Fluxo , Humanos , Ligantes , Receptores CCR1 , Receptores CCR5/genética , Receptores CCR5/metabolismo , Receptores de Quimiocinas/genética , Receptores de Quimiocinas/metabolismo , Transdução de Sinais , Transfecção
15.
J Physiol ; 514 ( Pt 3): 629-37, 1999 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-9882735

RESUMO

1. Whole-cell patch clamp recordings were used to investigate the modulation by reducing and oxidizing agents of recombinant human cardiac L-type Ca2+ channel alpha1C subunits stably expressed in human embryonic kidney (HEK 293) cells. 2. The oxidizing agents thimerosal (10 microM) and p-chloromercuribenzene sulphonic acid (PCMBS; 2 microM to 2 mM) caused irreversible inhibition of Ca2+ channel currents. The reducing agent 1,4-dithiothreitol (DTT; 2 mM) was without effect on Ca2+ channel currents, but reversed the inhibitory actions of thimerosal and PCMBS. 3. Ca2+ channel currents were also inhibited by pretreatment with the methanethiosulphonate compound (2-aminoethyl)methanethiosulphonate (MTSEA, 2.5 mM), but were unaffected by identical pretreatment with (2-sulphonatoethyl)methanethiosulphonate (MTSES, 10 mM). The effects of MTSEA could be fully reversed by DTT (2 mM). The degree of current inhibition caused by 200 microM PCMBS was not significantly affected by pretreatment with MTSEA, and following PCMBS treatment, MTSEA caused a similar degree of inhibition to that observed in cells that were not previously treated with PCMBS. These findings suggested that distinct thiol groups were modulated by these two agents. 4. Hypoxic inhibition of Ca2+ channel currents was unaffected by pretreatment of cells with MTSEA but was fully prevented by treatment with PCMBS. Our results indicate that distinct cysteine residues on the alpha1C subunit can undergo redox modulation and in so doing alter channel function. Some, but not all, of these residues appear to be associated with the mechanism underlying inhibition of this channel by hypoxia.


Assuntos
Canais de Cálcio/metabolismo , Hipóxia/metabolismo , Miocárdio/metabolismo , Oxidantes/farmacologia , Substâncias Redutoras/farmacologia , Bloqueadores dos Canais de Cálcio/farmacologia , Canais de Cálcio/química , Canais de Cálcio/efeitos dos fármacos , Canais de Cálcio Tipo L , Linhagem Celular , Cisteína/química , Estimulação Elétrica , Eletrofisiologia , Coração/efeitos dos fármacos , Humanos , Potenciais da Membrana/fisiologia , Oxirredução , Técnicas de Patch-Clamp , Proteínas Recombinantes/metabolismo
16.
Vet Rec ; 143(20): 550-2, 1998 Nov 14.
Artigo em Inglês | MEDLINE | ID: mdl-9854316

RESUMO

Paraplegia affected 14 hedgehogs (Erinaceus europaeus) in a wildlife rescue hospital over a period of six months. Postmortem examination revealed demyelination in the brain and spinal cord and an inflammatory response in the meninges, choroid plexus and CNS. The peripheral nervous system was not affected. In the spleen, lungs and liver there was an accumulation of megakaryocytes and other evidence of extramedullary haemopoiesis, but there was no haematological evidence of anaemia. The pattern of disease incidence and the nature of the changes in the CNS suggest they were of viral origin, but no causal agent was isolated and the possibility of a neurotoxin cause cannot be ruled out.


Assuntos
Sistema Nervoso Central/patologia , Doenças Desmielinizantes/veterinária , Ouriços , Animais , Doenças Desmielinizantes/patologia , Surtos de Doenças/veterinária
17.
Eur J Pharmacol ; 342(2-3): 353-8, 1998 Jan 26.
Artigo em Inglês | MEDLINE | ID: mdl-9548408

RESUMO

Inhibition of ion channels by the phosphodiesterase inhibitor 3-isobutyl-1-methylxanthine (IBMX) and related compounds has been demonstrated in various cell types, including the neuromuscular junction, GH3 cells and vascular smooth muscle cells. These effects may be unrelated to the actions of these compounds on cellular metabolism, intracellular Ca2+ stores and phosphodiesterase inhibition. In this study, the inhibition of recombinant human cardiac L-type Ca2+ channel alpha1C subunits by IBMX was examined using the whole-cell configuration of the patch clamp technique. Inhibition was repeatable, voltage-independent and associated with increased apparent channel inactivation. The actions of IBMX were unaffected in the presence of inhibitors of protein kinases A and G. The non-xanthine phosphodiesterase inhibitor rolipram had a small inhibitory effect on currents, but this was also unaffected by a protein kinase A inhibitor. These effects of IBMX could not be attributed to release of Ca2+ from intracellular stores. Our findings indicate that methylxanthines can inhibit the cardiac L-type Ca2+ channel alpha1C subunit in the absence of auxiliary subunits by an undetermined, possibly direct mechanism.


Assuntos
1-Metil-3-Isobutilxantina/farmacologia , Bloqueadores dos Canais de Cálcio/farmacologia , Canais de Cálcio/metabolismo , Miocárdio/metabolismo , Inibidores de Fosfodiesterase/farmacologia , Adenosina/antagonistas & inibidores , Bário/metabolismo , Canais de Cálcio/genética , Células Clonais , Flavinas/farmacologia , Coração/efeitos dos fármacos , Humanos , Potenciais da Membrana/efeitos dos fármacos , Técnicas de Patch-Clamp , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo
18.
Undersea Hyperb Med ; 24(3): 193-200, 1997 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-9308143

RESUMO

The nature of so-called autochthonous bubbles was investigated. Their presence in compressed/decompressed goats was compared with that in animals killed before decompression and in controls. Ten goats (group 1) were subjected to compression/decompression in air. Clinical signs of spinal decompression sickness usually occurred. Within 35 min of surfacing, the animals were given a lethal dose of thiopentone sodium, i.v.. Spinal cords were fixed by immersion in 10% formol saline. Histologically autochthonous bubbles appeared to arise from rupture of over-distended blood vessels. The incidence of grossly dilated empty vessels (GDEV) was recorded. Seven goats (group 2) were similarly compressed but killed before decompression. In five animals of group 1 there was a greater number of GDEV than in controls (group 3, seven animals) but in the other five animals the incidence was similar to the controls. The incidence of GDEV in group 2 was greater than in the controls (P < 0.05). The percentage of sections of spinal cord in which the meninges also contained GDEV was assessed. In all except two animals in group 1, the percentage was higher than in the controls, whereas in group 2 the percentage was higher than in the controls. The experiments show that autochthonous bubbles arise as an artifact and that intravascular bubbles arise in situ.


Assuntos
Doença da Descompressão/patologia , Paralisia/patologia , Doenças da Medula Espinal/patologia , Medula Espinal/irrigação sanguínea , Animais , Tecido Conjuntivo/patologia , Descompressão , Doença da Descompressão/complicações , Dilatação Patológica/etiologia , Dilatação Patológica/patologia , Feminino , Cabras , Masculino , Paralisia/etiologia , Doenças da Medula Espinal/etiologia , Doenças Vasculares/etiologia , Doenças Vasculares/patologia
19.
J Pharmacol Exp Ther ; 281(3): 1257-63, 1997 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9190861

RESUMO

The ability of angiotensin II (AII) to regulate [Ca++]i in human neuroblastoma (SH-SY5Y) cells stably expressing recombinant rat AT1A receptors was investigated using microfluorimetric methods, and compared to responses obtained by stimulation of native muscarinic receptors. Applications of AII or carbachol produced biphasic rises of [Ca++]i, but in Ca++-free solutions (containing 1 mM ethylene glycol-bis (beta-aminoethyl ether)N,N,N,'N'-tetraacetic acid), both agonists produced only transient monophasic rises of [Ca++]i, and second applications were without effect. Application of Ca++(o) (2.5 mM) to cells after exposure to either agonist produced a Ni2+-sensitive rise of [Ca++]i in the absence of agonist ("capacitative Ca++ influx"). After removal of Ca++(o), both AII and carbachol elicited a second rise of [Ca++]i. Thapsigargin (1 microM) prevented these second rises of [Ca++]i. During capacitative Ca++ influx, application of AII failed to produce a further rise of [Ca++]i. In contrast, carbachol produced a further rise of [Ca++]i, attributable to activation of both nicotinic and muscarinic receptors, because it was reduced (but not abolished) by mecamylamine (1 microM) and was observed when muscarine was used as the agonist. Thus, activation of recombinant AT1A and muscarinic receptors in SH-SY5Y cells leads to mobilization of Ca++ from a common intracellular pool, and stimulates capacitative Ca++ influx. Muscarinic (but not AII) receptor occupancy is capable of stimulating an additional Ca++ influx pathway.


Assuntos
Angiotensina II/farmacologia , Cálcio/metabolismo , Carbacol/farmacologia , Neuroblastoma/metabolismo , Receptores de Angiotensina/efeitos dos fármacos , Animais , Células Cultivadas/efeitos dos fármacos , Humanos , Ratos , Proteínas Recombinantes/metabolismo
20.
J Physiol ; 500 ( Pt 3): 551-6, 1997 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-9161974

RESUMO

1. Whole-cell patch clamp recordings were used to investigate the effects of hypoxia on recombinant human L-type Ca2+ channel alpha 1C subunits stably expressed in human embryonic kidney (HEK 293) cells. 2. Ca2+ channel currents were reversibly inhibited by hypoxia (PO2 < 90 mmHg). The degree of inhibition depended on the charge carrier used, Ca2+ currents being more O2 sensitive than Ba2+ currents. 3. Hypoxic inhibition of Ca2+ channel currents was more pronounced at lower activating membrane potentials (< or = +30 mV), and was associated with a slowing of activation kinetics. Current inactivation and deactivation were unaffected by hypoxia. 4. Since hypoxia similarly regulates native L-type Ca2+ channels in vascular smooth muscle cells, our results suggest that hypoxic regulation of L-type Ca2+ channels arises from modification of structural features of the alpha 1 subunit common to cardiac and smooth muscle L-type channels.


Assuntos
Canais de Cálcio/metabolismo , Hipóxia/fisiopatologia , Miocárdio/metabolismo , Animais , Bário/metabolismo , Células Cultivadas , Eletrofisiologia , Humanos , Rim/citologia , Rim/metabolismo , Cinética , Potenciais da Membrana/fisiologia , Fases de Leitura Aberta , Técnicas de Patch-Clamp , Proteínas Recombinantes/metabolismo , Xenopus laevis
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