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1.
International Journal of Oral Biology ; : 129-135, 2017.
Artigo em Coreano | WPRIM | ID: wpr-201471

RESUMO

The present study investigated the role of spinal glutamate recycling in the development of orofacial inflammatory pain or trigeminal neuropathic pain. Experiments were carried out on male Sprague-Dawley rats weighing between 230 and 280 g. Under anesthesia, a polyethylene tube was implanted in the atlanto-occipital membrane for intracisternal administration. IL-1β-induced inflammation was employed as an orofacial acute inflammatory pain model. IL-1β (10 ng) was injected subcutaneously into one vibrissal pad. We used the trigeminal neuropathic pain animal model produced by chronic constriction injury of the infraorbital nerve. DL-threo-β -benzyloxyaspartate (TBOA) or methionine sulfoximine (MSO) was administered intracisternally to block the spinal glutamate transporter and the glutamine synthetase activity in astroglia. Intracisternal administration of TBOA produced mechanical allodynia in naïve rats, but it significantly attenuated mechanical allodynia in rats with interleukin (IL)-1 β-induced inflammatory pain or trigeminal neuropathic pain. In contrast, intracisternal injection of MSO produced anti-allodynic effects in rats treated with IL-1β or with infraorbital nerve injury. Intracisternal administration of MSO did not produce mechanical allodynia in naive rats. These results suggest that blockade of glutamate recycling induced pro-nociception in naïve rats, but it paradoxically resulted in anti-nociception in rats experiencing inflammatory or neuropathic pain. Moreover, blockade of glutamate reuptake could represent a new therapeutic target for the treatment of chronic pain conditions.


Assuntos
Animais , Humanos , Masculino , Ratos , Sistema X-AG de Transporte de Aminoácidos , Anestesia , Astrócitos , Dor Crônica , Constrição , Glutamato-Amônia Ligase , Ácido Glutâmico , Hiperalgesia , Inflamação , Interleucinas , Membranas , Metionina Sulfoximina , Modelos Animais , Neuralgia , Polietileno , Ratos Sprague-Dawley , Reciclagem
2.
Journal of Southern Medical University ; (12): 2410-2413, 2009.
Artigo em Chinês | WPRIM | ID: wpr-325103

RESUMO

<p><b>OBJECTIVE</b>To explore the role of glial cell metabolism in the generation and regulation of central respiratory rhythm.</p><p><b>METHODS</b>The medulla oblongata slices (600-700 microm) containing the medial region of the nucleus retrofacialis (mNRF) with the hypoglossal nerve rootlets retained from 12 neonatal (0-3 days) Sprague-Dawley rats were prepared and perfused with modified Kreb's solution (MKS). Upon recording of respiratory rhythmical discharge activity (RRDA) of the rootlets of the hypoglossal nerve, the brain slices were treated with glial cell metabolism antagonist L-methionine sulfoximine (L-MSO, 50 micromol/L) for 20 min followed by application of glial cell metabolism agonist L-glutamine (L-GLN, 30 micromol/L) for 20 min, or with L-MSO for 20 min with additional L-GLN for 20 min. The changes in the RRDA of the rootlets of the hypoglossal nerve in response to the treatments were recorded.</p><p><b>RESULTS</b>L-MSO prolonged the respiratory cycle (RC) and expiratory time (TE), and reduced the integral amplitude (IA) and the inspiratory time (TI) in the brain slices. L-GLN induced a significant decrease in RC and TE, but IA and TI showed no obvious variations. The effect of L-MSO on the respiratory rhythm was reversed by the application of L-GLN.</p><p><b>CONCLUSION</b>Glial cell metabolism may play an important role in the modulation of RRDA in neonatal rat brainstem.</p>


Assuntos
Animais , Ratos , Animais Recém-Nascidos , Glutamina , Farmacologia , Técnicas In Vitro , Bulbo , Metabolismo , Fisiologia , Metionina Sulfoximina , Farmacologia , Neuroglia , Metabolismo , Periodicidade , Ratos Sprague-Dawley , Respiração
3.
Indian J Exp Biol ; 2000 Apr; 38(4): 373-8
Artigo em Inglês | IMSEAR | ID: sea-59195

RESUMO

Spontaneous mutants resistant to methionine sulfoximine (Msx), methyl alanine (Mal) and methyl ammonium chloride (Mac) were derived from A. chroococcum strain A103. Msx and Mal-resistant mutants expressed 1.73 to 10.98% of the fully derepressed nitrogenase activity when grown in Burk's medium containing ammonium acetate. Mac-resistant mutants did not express nitrogenase activity in ammonium acetate supplemented medium. The mutants excreted ammonia even after 2 days of growth and some mutants excreted more ammonia as compared to the parent. Selected mutants were inoculated on wheat (Triticum aestivum) and barley (Hordeum vulgare) under field conditions. Majority of the derepressed mutants increased grain yield of wheat and barley varying from 1.2 to 33.3%. However, host-dependent effects on grain yield were observed with different mutants. Two mutants, Mal 27 and Mac 19 showed significant increase in grain yields of both the crops. The results suggest that metabolic analogue-resistant mutants of Azotobacter have potential for use as a biofertilizer for cereal crops.


Assuntos
Alanina/análogos & derivados , Amônia/metabolismo , Azotobacter/efeitos dos fármacos , Grão Comestível/microbiologia , Resistência Microbiana a Medicamentos/genética , Metionina Sulfoximina/farmacologia , Metilaminas/farmacologia , Mutação , Fixação de Nitrogênio , Nitrogenase/genética
4.
Indian J Biochem Biophys ; 1990 Jun; 27(3): 164-6
Artigo em Inglês | IMSEAR | ID: sea-28469

RESUMO

Effects of methionine sulphoximine (MSX) on glutamine synthetase activity and ammonia accumulation in the leaves of barley, sorghum and Moricandia arvensis were studied. Glutamine synthetase activity of sorghum leaves was relatively resistant to MSX treatment during initial stages. All the three plant species exhibited considerable accumulation of ammonia arising from non-photorespiratory sources, in response to MSX treatment. Minimal estimates of the rate of glycine decarboxylation were made employing MSX and isonicotinyl hydrazide together in the treatment solution. Changes in the pool sizes of amino acids involved in photorespiratory nitrogen metabolism as affected by MSX have also been investigated.


Assuntos
Aminoácidos/metabolismo , Amônia/metabolismo , Glutamato-Amônia Ligase/metabolismo , Hordeum/metabolismo , Metionina Sulfoximina/farmacologia , Plantas/efeitos dos fármacos
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