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1.
Neuropharmacology ; 66: 202-14, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-22551786

RESUMEN

Evidence suggests that 30-50% of patients suffering from major depressive disorder (MDD) are classified as suffering from treatment resistant depression (TRD) as they have an inadequate response to standard antidepressants. A key feature of this patient population is the increased incidence of co-morbid symptoms like anxiety and pain. Recognizing that current standards of care are largely focused on monoaminergic mechanisms of action (MOAs), innovative approaches to drug discovery for TRD are targeting glutamate hyperfunction. Here we describe the in vitro and in vivo profile of GRN-529, a novel negative allosteric modulator (NAM) of metabotropic glutamate receptor 5 (mGluR5). In cell based pharmacology assays, GRN-529 is a high affinity (Ki 5.4 nM), potent (IC50 3.1 nM) and selective (>1000-fold selective vs mGluR1) mGluR5 NAM. Acute administration of GRN-529 (0.1-30 mg/kg p.o.) had dose-dependent efficacy across a therapeutically relevant battery of animal models, comprising depression (decreased immobility time in tail suspension and forced swim tests) and 2 of the co-morbid symptoms overrepresented in TRD, namely anxiety (attenuation of stress-induced hyperthermia, and increased punished crossings in the four plate test) and pain (reversal of hyperalgesia due to sciatic nerve ligation or inflammation). The potential side effect liability of GRN-529 was also assessed using preclinical models: GRN-529 had no effect on rat sexual behavior or motor co-ordination (rotarod), however it impaired cognition in mice (social odor recognition). Efficacy and side effects of GRN-529 were compared to standard of care agents (antidepressant, anxiolytic or analgesics) and the tool mGluR5 NAM, MTEP. To assess the relationship between target occupancy and efficacy, ex vivo receptor occupancy was measured in parallel with efficacy testing. This revealed a strong correlation between target engagement, exposure and efficacy across behavioral endpoints, which supports the potential translational value of PET imaging to dose selection in patients. Collectively this broad spectrum profile of efficacy of GRN-529 supports our hypothesis that negative allosteric modulation of mGluR5 could represent an innovative therapeutic approach to the treatment of TRD. This article is part of a Special Issue entitled 'Metabotropic Glutamate Receptors'.


Asunto(s)
Regulación Alostérica/efectos de los fármacos , Trastorno Depresivo Resistente al Tratamiento/tratamiento farmacológico , Antagonistas de Aminoácidos Excitadores/uso terapéutico , Receptores de Glutamato Metabotrópico/antagonistas & inhibidores , Regulación Alostérica/fisiología , Analgésicos/farmacología , Animales , Ansiolíticos/farmacología , Antidepresivos/efectos adversos , Antidepresivos/farmacología , Antidepresivos/uso terapéutico , Conducta Animal/efectos de los fármacos , Benzamidas/efectos adversos , Benzamidas/farmacología , Benzamidas/uso terapéutico , Calcio/metabolismo , Trastorno Depresivo Resistente al Tratamiento/metabolismo , Trastorno Depresivo Resistente al Tratamiento/fisiopatología , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos/métodos , Evaluación Preclínica de Medicamentos/psicología , Antagonistas de Aminoácidos Excitadores/efectos adversos , Antagonistas de Aminoácidos Excitadores/farmacología , Ácido Glutámico/farmacología , Células HEK293 , Humanos , Ratones , Piridinas/efectos adversos , Piridinas/farmacología , Piridinas/uso terapéutico , Ensayo de Unión Radioligante/métodos , Ratas , Receptor del Glutamato Metabotropico 5 , Receptores de Glutamato Metabotrópico/metabolismo , Receptores de Glutamato Metabotrópico/fisiología
2.
Allergy ; 48(8): 624-6, 1993 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-8116861

RESUMEN

Aeroallergen-induced infiltration of eosinophils in the bronchoalveolar lavage fluid (BALF) in guinea pigs was used as a marker of bronchial inflammation. Drugs were administered orally 4 h after aeroallergen challenge. Allergic bronchial eosinophilia in guinea pigs was inhibited by orally administered dexamethasone and methylprednisolone. Terfenadine (a newer H1-receptor antagonist), theophylline (a nonspecific phosphodiesterase inhibitor), and salbutamol (a beta 2-agonist) did not influence allergic eosinophilic infiltration. Many of these agents, administered prophylactically, have been reported to suppress allergic eosinophilic infiltration in the BALF of guinea pigs. Methylprednisolone, a steroid, inhibits allergic bronchial eosinophilia regardless of the time of administration; that is, 2 h before or 4 h after aeroallergen challenge. The therapeutic approach used in this study may facilitate drug discovery for bronchial inflammation/asthma.


Asunto(s)
Antiinflamatorios/uso terapéutico , Asma/tratamiento farmacológico , Hiperreactividad Bronquial/tratamiento farmacológico , Eosinofilia/tratamiento farmacológico , Albuterol/uso terapéutico , Alérgenos/administración & dosificación , Animales , Antiinflamatorios/administración & dosificación , Asma/patología , Hiperreactividad Bronquial/patología , Líquido del Lavado Bronquioalveolar/citología , Dexametasona/uso terapéutico , Modelos Animales de Enfermedad , Esquema de Medicación , Evaluación Preclínica de Medicamentos , Eosinofilia/patología , Eosinófilos/efectos de los fármacos , Cobayas , Masculino , Metilprednisolona/uso terapéutico , Ovalbúmina/inmunología , Terfenadina/uso terapéutico , Teofilina/uso terapéutico
3.
J Bone Miner Res ; 3(2): 127-32, 1988 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-3213607

RESUMEN

Forty-one women with idiopathic postmenopausal osteoporosis have been followed for 2 years after initiation of sodium fluoride at 40-50 mg/day, given together with a daily calcium supplement of 1 gram and vitamin D2, at 50,000 IU weekly. Histological and histomorphometric analyses were done on bone biopsies taken prior to and after 1 year of treatment (mean 1.25 +/- 0.35 years). Thirty patients (74%) developed the histological fluoride effect of hyperosteoidosis, while the remaining 11 patients (26%) had no change from pretreatment biopsies. Hyperosteoidosis was based on increased values for osteoid volume and/or thickened osteoid with greater than 3 lamellar bands. Based on previously reported findings, this histological evidence of hypersoteoidosis within 12-18 months of initiation of therapy provides a useful predictor of ultimate satisfactory fluoride response in terms of bone mineral accretion. No increases in bone mass (measured by neutron activation analysis) were observed at the time of the posttreatment biopsy but, according to this previous work, increases are anticipated over a further 2-3 years of treatment. Factors affecting the development of hyperosteoidosis were analyzed. Hyperosteoidosis was associated with a significantly higher dose of sodium fluoride and a significantly higher level of bone fluoride retention but without significant increase in fasting serum fluoride. Results suggest that fluoride retention depends not only on fluoride dose but also on body size, renal function, and intestinal absorptions of calcium and fluoride. There were no differences in the initial investigations between patients with and without hyperosteoidosis, with respect to age, years of postmenopause, estrogen use, initial biochemistry, or initial bone histology.(ABSTRACT TRUNCATED AT 250 WORDS)


Asunto(s)
Huesos/patología , Absorción Intestinal , Osteoporosis/tratamiento farmacológico , Fluoruro de Sodio/uso terapéutico , Biopsia , Huesos/efectos de los fármacos , Huesos/metabolismo , Femenino , Humanos , Menopausia , Persona de Mediana Edad , Osteoporosis/fisiopatología , Fluoruro de Sodio/farmacocinética
4.
Life Sci ; 34(26): 2627-31, 1984 Jun 25.
Artículo en Inglés | MEDLINE | ID: mdl-6588287

RESUMEN

Platelet deficient serum prepared from rats subjected to acute electrical stimulation of the lateral hypothalamus demonstrated mitogenic activity when added to incubating media supporting growth of homologous arterial smooth muscle cells in vitro. This activity did not appear to be related to the presence of platelet-derived growth factor, hyperlipidemic lipoproteins or increased amounts of insulin. Plasma arginine vasopressin concentration was elevated in these animals, but further investigation is required to determine if this elevation is causally related. Since hypothalamic stimulation is also associated with severe endothelial injury in vivo, the mitogenic activity of the blood of such animals could induce proliferation of SMC which have migrated into the arterial intima. Such features have been observed in chronically stimulated animals and may be of relevance for the role of neural factors in atherogenesis.


Asunto(s)
Aorta/citología , Sangre , Hipotálamo/fisiología , Músculo Liso Vascular/citología , Animales , Arginina Vasopresina/sangre , División Celular , Células Cultivadas , Colesterol/sangre , HDL-Colesterol , VLDL-Colesterol , Estimulación Eléctrica , Lipoproteínas HDL/sangre , Lipoproteínas VLDL/sangre , Masculino , Ratas , Ratas Endogámicas
5.
Metabolism ; 31(11): 1121-7, 1982 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-7132739

RESUMEN

Plasma levels of the vitamin D metabolites were related to changes in bone morphology during the development of rickets in rats deprived of phosphorus and vitamin D. Weanling rats were studied at 1, 3, and 5 wk after onset of diets deficient in phosphorus or in both phosphorus and vitamin D. Bone histology and morphometry were carried out and measurements were made of 45Ca and 32P absorption, serum Ca and P, and plasma 25(OH)D3, 24,25(OH)2D3 and 1,25(OH)2D3. After 1 wk of vitamin D restriction, the plasma levels of 25(OH)D3 and 24,25(OH)2D3 were non-detectable (less than 0.5 and less than 0.8 ng/ml). The plasma 1,25(OH)2D3 level was elevated at 1 wk (105.5 pg/ml) and fell to 19 pg/ml by 5 wk. At 1 wk mild rachitic lesions in epiphyseal cartilage were observed despite the elevated 1,25(Oh)D3 level. Serum Ca and P levels and values for 45CA and 32P absorption decreased and the severity of the rickets increased with the fall in plasma levels of 1,25(OH)2D3. In Vitamin D replete, phosphate deficient rats the epiphyseal cartilage was normal throughout the 5 wk study period. Our results provide further evidence that physiological levels of 1,25 (OH)2 D3 will not prevent rickets without adequate plasma concentrations of either 25(OH)D3 or 24,25(OH)2D3.


Asunto(s)
Fósforo/deficiencia , Raquitismo/sangre , Deficiencia de Vitamina D/sangre , Vitamina D/sangre , Animales , Calcio/metabolismo , Cartílago/patología , Femenino , Fémur/patología , Fósforo/metabolismo , Ratas , Ratas Endogámicas , Raquitismo/patología , Deficiencia de Vitamina D/patología
6.
Atherosclerosis ; 41(1): 41-51, 1982 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-7073793

RESUMEN

Experimental animals fed atherogenic diets show endothelial damage, impairment of endothelial regeneration and plasma lipid changes characterized by elevation of LDL and decrease of HDL cholesterol concentrations. Previous studies in this laboratory disclosed that chronic electrical stimulation of the lateral hypothalamus was associated with electron-microscopic evidence of endothelial injury in rats and squirrel monkeys maintained on basal (low fat/cholesterol-free) diets. In the present investigation squirrel monkeys fed similar diets supplemented with "modest" amounts of caloric fat and cholesterol were subjected to chronic lateral hypothalamic stimulation for periods as long as 20 months with the expectation that endothelial injury would be greater than in the absence of the supplements. The expectations were not substantiated. Endothelium was found to be surprisingly intact by electron microscopy and similar to that of implanted nonstimulated controls. A further observation of interest was the cholesterolemic response, notably in the HDL fraction, observed in both groups, but more striking in experimental animals. The data suggest that an interaction between a modified lipid/cholesterol diet and hypothalamic stimulation may lead to elevation of plasma HDL cholesterol concentration and preservation of endothelial integrity. Further investigation is required to determine whether these two events are causally related.


Asunto(s)
Aorta/anatomía & histología , Colesterol/análisis , Dieta Aterogénica , Hipotálamo/fisiología , Lipoproteínas HDL/análisis , Lipoproteínas/análisis , Animales , Aorta/ultraestructura , HDL-Colesterol , Estimulación Eléctrica , Endotelio/anatomía & histología , Endotelio/ultraestructura , Lipoproteínas/sangre , Masculino , Microscopía Electrónica , Saimiri/fisiología
7.
Atherosclerosis ; 39(3): 329-44, 1981 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-7259817

RESUMEN

The role of neurogenic factors in the development of atherosclerosis has not previously been studied in detail. In recent years evidence has accumulated to implicate endothelial injury as a primary stimulus for the proliferation of myo-intimal cells resulting in the formation of the early morphologic lesion. In the present investigation, the effect on aortic endothelial morphology of repetitive electrical stimulation of the lateral hypothalamus in the conscious, unrestrained squirrel monkey, maintained on a cholesterol-free low-fat diet, has been studied. Stimulation was performed with a self-powered, miniaturized electronic stimulator connected to indwelling electrodes. Implanted nonstimulated animals served as controls. Endothelial injury in the form of cell degeneration, denudation, with plasma insudation and partial junctional separation were observed electron-microscopically in stimulated animals compared with controls. These alterations were found to be independent of hypercholesterolemia and/or hypertension. Possible pathways for the induction of injury in this neurogenic model are: (1) direct, through neural circuits from the brain to the vessel wall, and (2) indirect, by elaboration of angiopathic substances inside or outside of the CNS, released into the circulation and transported to the vessel wall where they exert their effects. Reversibility of the endothelial injury progression to established lesions and mechanisms involved remain to be determined in further investigations.


Asunto(s)
Vasos Sanguíneos/anatomía & histología , Hipotálamo/fisiología , Animales , Aorta/anatomía & histología , Presión Sanguínea , Colesterol/sangre , Dieta , Estimulación Eléctrica , Endotelio/citología , Masculino , Saimiri
8.
Calcif Tissue Int ; 33(2): 167-72, 1981.
Artículo en Inglés | MEDLINE | ID: mdl-6783273

RESUMEN

Using the technique of short interval sequential tetracycline labeling, it was documented that the apposition of mineralized bone matrix in adult male Sprague-Dawley rats was inhibited by hydrocortisone. The inhibition occurred as early as six days after the onset of the treatment and was dose dependent over a dose range of 0.62 to 20 mg per kg body weight per day. Vitamin D2 supplements by injection protected bone from this hydrocortisone action. 64 I. U. of vitamin D2 injected daily was able to prevent the inhibition of bone apposition by 20 mg per kg body weight per day of hydrocortisone. The results imply that vitamin D or its metabolites may compete with hydrocortisone in some cellular mechanisms and support the usefulness of vitamin D supplements in the treatment and the prevention of steroid-induced osteoporosis.


Asunto(s)
Huesos/fisiología , Ergocalciferoles/farmacología , Hidrocortisona/farmacología , Animales , Peso Corporal/efectos de los fármacos , Huesos/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Interacciones Farmacológicas , Cinética , Masculino , Ratas , Tetraciclina
9.
Metabolism ; 29(12): 1225-33, 1980 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7453566

RESUMEN

It has been widely believed that phosphate deficiency causes osteomalacia. Based on this belief, the rickets of familial hypophosphatemia has been attributed to phosphate deficiency associated with the hypophosphatemia. The present studies on rats have, however, demonstrated significant differences between the effects of phosphate deficiency on bone metabolism and the characteristic features of rickets. Weanling rats, maintained on a mildly phosphate deficient diet, had hypercalcemia and hypophosphatemia, and impairment of body growth, bone growth, and bone mineralization. The maximum effect was observed at 5 wk; between 5 and 20 wk the rats improved despite persistent hypophosphatemia. Histologically, at 5 wk the bone showed thick unmineralized osteoid seams covering most bone surfaces, but the epiphyseal cartilage was normal. In addition, the excess osteoid readily incorporated tetracycline indicating normal mineralization and, based on a new sequential pulse labeling technique, the linear bone apposition rate (LBA) was significantly (p < 0.001) increased above control values. This increase was observed within the initial 4 days of phosphate (P) deficiency and persisted up to 15 wk. This effect of P deficiency on LBA was dependent on vitamin D activity. At 4 wk, the mean LBA was 0.106 +/- 0.003 (1 SE) in control rats, 0.149 +/- 0.008 microns/hr in P deficient rats, 0.083 +/- 0.004 microns/hr in vitamin D deficient rats and 0.086 +/- 0.006 microns/hr in rats deficient in both P and vitamin D. We have reported a similar increase in LBA with parathyroid hormone activity. With vitamin D deficiency, phosphate deficient rats showed all the characteristic features of rickets; disorganization of epiphyseal cartilage, excessive unmineralized osteoid, and reduced mineralization based on the incorporation of tetracycline. We conclude that the effects of phosphate deficiency on bone metabolism more closely resembles the effects of PTH activity than the characteristic effects of osteomalacia and rickets.


Asunto(s)
Huesos/metabolismo , Fosfatos/deficiencia , Deficiencia de Vitamina D/metabolismo , Animales , Calcio/metabolismo , Femenino , Fémur/metabolismo , Fémur/patología , Histocitoquímica , Cinética , Minerales/metabolismo , Fósforo/metabolismo , Ratas , Tetraciclinas/metabolismo , Deficiencia de Vitamina D/patología
10.
Ann Intern Med ; 92(3): 343-50, 1980 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-6766694

RESUMEN

We have prospectively investigated calcium and bone metabolism in 16 patients receiving total parenteral nutrition for periods ranging from 7 to 89 months. In 12 patients, bone biopsies at 6 to 73 months after the start of parenteral nutrition showed osteomalacia. Plasma 25-hydroxyvitamin D levels were normal in all patients. Seven persons developed hypercalcemia, and 10 had hypercalciuria with a negative calcium balance. Serum phosphorus was normal and plasma parathyroid hormone level, normal or decreased. Three patients with the severest form of the disease had vitamin D withdrawn from their solutions. Subsequently, urinary calcium decreased, and serum calcium became normal; two persons reverted to a positive calcium balance. Thus, patients receiving total parenteral nutrition may develop metabolic bone disease characterized by osteomalacia, hypercalcemia, hypercalciuria, and a negative calcium balance. This may be caused by both defective mineralization and increased bone resorption induced by vitamin D, its metabolites, or another unrecognized factor.


Asunto(s)
Enfermedades Óseas Metabólicas/etiología , Nutrición Parenteral Total/efectos adversos , Nutrición Parenteral/efectos adversos , Adulto , Anciano , Enfermedades Óseas Metabólicas/metabolismo , Resorción Ósea/etiología , Calcio/metabolismo , Femenino , Humanos , Hidroxicolecalciferoles/metabolismo , Enfermedades Intestinales/terapia , Masculino , Persona de Mediana Edad , Osteomalacia/etiología , Hormona Paratiroidea/metabolismo , Fósforo/metabolismo , Vitamina D/administración & dosificación , Vitamina D/efectos adversos
11.
Can Med Assoc J ; 118(6): 635-8, 1978 Mar 18.
Artículo en Inglés | MEDLINE | ID: mdl-418865

RESUMEN

Long-term anticonvulsant drug therapy may lead to abnormalities of calcium metabolism resulting in osteomalacia. The prevalence and severity of altered calcium metabolism was studied in an adult outpatient population of persons with epilepsy receiving anticonvulsant therapy for a minimum of 2 years. Assessment of calcium metabolism was based on serum concentrations of calcium, phosphorus, alkaline phosphatase and 25-hydroxycholecalciferol and of plasma parathyroid hormone, intestinal absorption of isotopic calcium and skeletal bone mineral mass as determined by in vivo neutron activation or x-ray photodensitometry.Thirty-nine patients who had been receiving anticonvulsant therapy for an average of 20 years were studied; none had clinical evidence of metabolic bone disease. Decreased serum calcium concentration was noted in 10%, decreased serum phosphorus concentration in 10% and elevated serum alkaline phosphatase concentration in 44%. The mean serum 25-hydroxycholecalciferol concentration was significantly lower (P < 0.001) than in a control group (11.6 v. 19.6 mg/mL). None of 18 patients studied had an increased plasma concentration of parathyroid hormone, and only 1 of 17 patients had decreased intestinal absorption of isotopic calcium. Bone mineral mass was decreased in 44% of 32 patients studied.It was concluded that long-term treatment with anticonvulsant drugs leads to mild abnormalities of calcium metabolism and decreased bone mineral mass in a substantial percentage of adult outpatients with epilepsy. These abnormalities probably predispose the patients to the development of clinically significant metabolic bone disease.


Asunto(s)
Anticonvulsivantes/efectos adversos , Trastornos del Metabolismo del Calcio/inducido químicamente , Epilepsia/tratamiento farmacológico , Adulto , Anciano , Fosfatasa Alcalina/sangre , Atención Ambulatoria , Anticonvulsivantes/administración & dosificación , Anticonvulsivantes/uso terapéutico , Enfermedades Óseas/inducido químicamente , Huesos/análisis , Calcio/sangre , Calcio/metabolismo , Epilepsia/sangre , Femenino , Humanos , Hidroxicolecalciferoles/sangre , Cuidados a Largo Plazo , Masculino , Persona de Mediana Edad , Minerales/análisis , Fósforo/sangre
12.
Can J Physiol Pharmacol ; 53(1): 137-43, 1975 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-1139439

RESUMEN

Measurements were made of duodenal calcium-binding protein (CaBP) on rats during development of rickets and, subsequently, following vitamin-D2 treatment. Results showed a poor inverse correlation between duodenal CaBP and rickets. In rats fed a phosphate-deficient rachitogenic diet, duodenal CaBP concentration finally fell below detectable limits, but CaBP was still readily measurable 2 weeks after rickets was clearly established. Following a massive dose of vitamin D2 (50 000 I.U.) to rachitic animals, CaBP was formed. However, a small dose of vitamin D2 (500 I.U. daily for 4 days) was insufficient to demonstrate CaBP synthesis than vitamin-D treatment alone. The rachitogenic diet supplemented with phosphate, which caused osteoporosis but not rickets, inhibited CaBP synthesis. The results suggest that nutritional deficiencies from the rachitogenic diet, in addition to vitamin-D deficiency, inhibited CaBP synthesis.


Asunto(s)
Calcio/metabolismo , Dieta , Mucosa Intestinal/metabolismo , Proteínas/metabolismo , Raquitismo/metabolismo , Animales , Huesos/patología , Duodeno/metabolismo , Masculino , Fosfatos/farmacología , Unión Proteica , Biosíntesis de Proteínas , Ratas , Raquitismo/patología , Vitamina D/farmacología , Deficiencia de Vitamina D/metabolismo
13.
Can J Physiol Pharmacol ; 53(1): 144-9, 1975 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-1139440

RESUMEN

Experiments were carried out in pigs to investigate the relationship between concentration of intestinal calcium-binding protein (CaBP) and the presence of rickets. Pigs made rachitic by a diet deficient in calcium and in vitamin D had concentrations of intestinal CaBP no less than values obtained on control pigs. These experiments, together with earlier work on rats (Can. J. Physiol. Pharmacol. 1975. 53, 137--143), demonstrate a poor inverse correlation between levels of intestinal CaBP and rickets.


Asunto(s)
Calcio/metabolismo , Dieta , Mucosa Intestinal/metabolismo , Proteínas/metabolismo , Raquitismo/metabolismo , Animales , Huesos/patología , Calcio/deficiencia , Duodeno/metabolismo , Femenino , Hígado/metabolismo , Fósforo/sangre , Embarazo , Unión Proteica , Raquitismo/patología , Porcinos , Vitamina D/metabolismo , Deficiencia de Vitamina D/metabolismo
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