RESUMEN
BACKGROUND AND PURPOSE: Cysteinyl leukotrienes (CysLTs) have been implicated in the pathophysiology of inflammatory and cardiovascular disorders. Their actions are mediated by CysLT(1) and CysLT(2) receptors. Here we report the discovery of 3-({[(1S,3S)-3-carboxycyclohexyl]amino}carbonyl)-4-(3-{4-[4-(cyclo-hexyloxy)butoxy]phenyl}propoxy) benzoic acid (HAMI3379), the first potent and selective CysLT(2) receptor antagonist. EXPERIMENTAL APPROACH: Pharmacological characterization of HAMI3379 was performed using stably transfected CysLT(1) and CysLT(2) receptor cell lines, and isolated, Langendorff-perfused, guinea pig hearts. KEY RESULTS: In a CysLT(2) receptor reporter cell line, HAMI3379 antagonized leukotriene D(4)- (LTD(4)-) and leukotriene C(4)- (LTC(4)-) induced intracellular calcium mobilization with IC(50) values of 3.8 nM and 4.4 nM respectively. In contrast, HAMI3379 exhibited very low potency on a recombinant CysLT(1) receptor cell line (IC(50) > 10 000 nM). In addition, HAMI3379 did not exhibit any agonistic activity on both CysLT receptor cell lines. In binding studies using membranes from the CysLT(2) and CysLT(1) receptor cell lines, HAMI3379 inhibited [(3)H]-LTD(4) binding with IC(50) values of 38 nM and >10 000 nM respectively. In isolated Langendorff-perfused guinea pig hearts HAMI3379 concentration-dependently inhibited and reversed the LTC(4)-induced perfusion pressure increase and contractility decrease. The selective CysLT(1) receptor antagonist zafirlukast was found to be inactive in this experimental setting. CONCLUSIONS AND IMPLICATIONS: HAMI3379 was identified as a potent and selective CysLT(2) receptor antagonist, which was devoid of CysLT receptor agonism. Using this compound, we showed that the cardiac effects of CysLTs are predominantly mediated by the CysLT(2) receptor.
Asunto(s)
Ácidos Ciclohexanocarboxílicos/farmacología , Antagonistas de Leucotrieno/farmacología , Ácidos Ftálicos/farmacología , Receptores de Leucotrienos/efectos de los fármacos , Animales , Células CHO , Calcio/metabolismo , Línea Celular , Cricetinae , Cricetulus , Ácidos Ciclohexanocarboxílicos/administración & dosificación , Relación Dosis-Respuesta a Droga , Cobayas , Corazón/efectos de los fármacos , Humanos , Indoles , Concentración 50 Inhibidora , Antagonistas de Leucotrieno/administración & dosificación , Leucotrieno C4/metabolismo , Leucotrieno D4/metabolismo , Masculino , Contracción Miocárdica/efectos de los fármacos , Fenilcarbamatos , Ácidos Ftálicos/administración & dosificación , Unión Proteica , Receptores de Leucotrienos/metabolismo , Sulfonamidas , Compuestos de Tosilo/farmacologíaRESUMEN
A stably transfected soluble guanylate cyclase (sGC, alpha1 and beta1 subunits of the rat lung enzyme)-overexpressing CHO cell line was generated for the characterization of different types of activators of the soluble guanylate cyclase. Polyclonal antibodies directed against both subunits of the rat enzyme were used to detect both subunits in the cytosol of the transfected CHO cells. We studied the effects of different nitric oxide (NO) donors like SNP and DEA/NO and, in particular, the direct, NO-independent stimulator of the soluble guanylate cyclase 3-(5'-hydroxymethyl-2'furyl)-1-benzyl indazole (YC-1), on intracellular guanosine 3',5'-cyclic monophosphate (cGMP) production. DEA/NO (0.01-3 microM), SNP (1-10 microM), and YC-1 (1-10 microM) induced a concentration-dependent intracellular cGMP increase with maximal effects of 16-fold (3 microM DEA/NO), 8-fold (10 microM SNP), and 6-fold (10 microM YC-1) stimulation compared to controls, respectively. In addition, a synergistic effect of the combination of the NO donor and YC-1 could be observed with a maximal stimulation of 64-fold by SNP (10 microM) and YC-1 (10 microM). 1H-(1,2,4)-Oxadiazolo-(4,3-a)-6-bromo-quinoxazin-1-one (ODQ, 10 microM), a potent and selective inhibitor of sGC, inhibited both the single effects of NO donors [DEA/NO (3 microM), 77%; SNP (3 microM), 83%] and YC-1 [YC-1 (3 microM), 82%], but moreover the synergistic effects between NO donors and YC-1 [DEA/NO (3 microM) + YC-1 (3 microM), 81%; SNP (3 microM) + YC-1 (3 microM),89%] on intracellular cGMP production. In summary,we have generated a simple, sensitive, and useful bioassay method to characterize all types of sGC activators on the cellular level without the need of primary cell culture, several transfections, or purifying enzyme from biological materials.
Asunto(s)
Células CHO , Guanilato Ciclasa/genética , Secuencia de Aminoácidos , Animales , Cricetinae , GMP Cíclico/metabolismo , Inhibidores Enzimáticos/farmacología , Guanilato Ciclasa/antagonistas & inhibidores , Guanilato Ciclasa/química , Datos de Secuencia Molecular , Donantes de Óxido Nítrico/farmacología , Fragmentos de Péptidos/química , Ratas , TransfecciónRESUMEN
Tissue expression and distribution of the high-conductance Ca(2+)-activated K+ channel Slo was investigated in rat brain by immunocytochemistry, in situ hybridization, and radioligand binding using the novel high-affinity (Kd 22 pM) ligand [3H]iberiotoxin-D19C ([3H]IbTX-D19C), which is an analog of the selective maxi-K peptidyl blocker IbTX. A sequence-directed antibody directed against Slo revealed the expression of a 125 kDa polypeptide in rat brain by Western blotting and precipitated the specifically bound [3H]IbTX-D19C in solubilized brain membranes. Slo immunoreactivity was highly concentrated in terminal areas of prominent fiber tracts: the substantia nigra pars reticulata, globus pallidus, olfactory system, interpeduncular nucleus, hippocampal formation including mossy fibers and perforant path terminals, medial forebrain bundle and pyramidal tract, as well as cerebellar Purkinje cells. In situ hybridization indicated high levels of Slo mRNA in the neocortex, olfactory system, habenula, striatum, granule and pyramidal cell layer of the hippocampus, and Purkinje cells. The distribution of Slo protein was confirmed in microdissected brain areas by Western blotting and radioligand-binding studies. The latter studies also established the pharmacological profile of neuronal Slo channels. The expression pattern of Slo is consistent with its targeting into a presynaptic compartment, which implies an important role in neural transmission.
Asunto(s)
Axones/química , Química Encefálica , Calcio/fisiología , Proteínas de la Membrana/análisis , Terminaciones Nerviosas/química , Proteínas del Tejido Nervioso/análisis , Canales de Potasio Calcio-Activados , Canales de Potasio/análisis , Potasio/metabolismo , Secuencia de Aminoácidos , Animales , Anticuerpos Monoclonales/inmunología , Secuencia de Bases , Unión Competitiva , Western Blotting , Compartimento Celular , Caribdotoxina/metabolismo , Hibridación in Situ , Activación del Canal Iónico/fisiología , Subunidades alfa de los Canales de Potasio de Gran Conductancia Activados por Calcio , Canales de Potasio de Gran Conductancia Activados por el Calcio , Masculino , Proteínas de la Membrana/efectos de los fármacos , Proteínas de la Membrana/inmunología , Datos de Secuencia Molecular , Proteínas del Tejido Nervioso/inmunología , Especificidad de Órganos , Fragmentos de Péptidos/inmunología , Péptidos/metabolismo , Canales de Potasio/efectos de los fármacos , Canales de Potasio/inmunología , ARN Mensajero/análisis , Ensayo de Unión Radioligante , Ratas , Ratas Sprague-Dawley , Proteínas Recombinantes/farmacologíaRESUMEN
A novel potassium channel beta-subunit (Kv beta 3) was cloned from rat brain being the third member of a Kv beta subunit gene family. It is a protein of 403 amino acid residues with a 68% amino acid sequence homology to Kv beta 1.1. Kv beta 3 is primarily expressed in rat brain having a distribution distinct to those of Kv beta 1.1 and Kv beta 2. This subunit also has a long N-terminal structure and induces inactivation in N-terminal deleted Kv1.4 but not in other members of the Kv1 channel family. Similarly to Kv beta 1.1, the Kv beta 3-induced inactivation is regulated by the intracellular redox potential.
Asunto(s)
Química Encefálica , Proteínas del Tejido Nervioso/aislamiento & purificación , Canales de Potasio/aislamiento & purificación , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Encéfalo/anatomía & histología , ADN Complementario/genética , Conductividad Eléctrica , Biblioteca de Genes , Subunidades beta de los Canales de Potasio de Gran Conductancia Activados por el Calcio , Datos de Secuencia Molecular , Familia de Multigenes , Proteínas del Tejido Nervioso/genética , Proteínas del Tejido Nervioso/metabolismo , Oocitos , Técnicas de Placa-Clamp , Canales de Potasio/genética , Canales de Potasio/metabolismo , Conformación Proteica , ARN Mensajero/análisis , Ratas , Análisis de Secuencia de ADN , Homología de Secuencia de Aminoácido , Distribución Tisular , XenopusRESUMEN
A large variety of potassium channels is involved in regulating integration and transmission of electrical signals in the nervous system. Different types of neurons, therefore, require specific patterns of potassium channel subunits expression and specific regulation of subunit coassembly into heteromultimeric channels, as well as subunit-specific sorting and segregation. This was investigated by studying in detail the expression of six different alpha-subunits of voltage-gated potassium channels in the rat hippocampus, cerebellum, olfactory bulb and spinal cord, combining in situ hybridization and immunocytochemistry. Specific polyclonal antibodies were prepared for five alpha-subunits (Kv1.1, Kv1.2, Kv1.3 Kv1.4, Kv1.6) of the Shaker-related subfamily of rat Kv channels, which encode delayed-rectifier type and rapidly inactivating A-type potassium channels. Their distribution was compared to that of an A-type potassium channel (Kv3.4), belonging to the Shaw-related subfamily of rat Kv channels. Our results show that these Kv channel alpha-subunits are differentially expressed in rat brain neurons. We did not observe in various neurons a stereotypical distribution of Kv channel alpha-subunits to dendritic and axonal compartments, but a complex differential subcellular subunit distribution. The different Kv channel subunits are targeted either to presynaptic or to postsynaptic domains, depending on neuronal cell type. Thus, distinct combinations of Kv1 alpha-subunits are co-localized in different neurons. The implications of these findings are that both differential expression and assembly as well as subcellular targeting of Kv channel alpha-subunits may contribute to Kv channel diversity and thereby to presynaptic and postsynaptic membrane excitability.
Asunto(s)
Encéfalo/metabolismo , Canales de Potasio/metabolismo , Animales , Cerebelo/metabolismo , Femenino , Inmunohistoquímica , Hibridación in Situ , Masculino , Bulbo Olfatorio/metabolismo , Ratas , Ratas WistarRESUMEN
We have cloned a mammalian (rat) homologue of Drosophila ether á go-go (eag) cDNA, which encodes a distinct type of voltage activated potassium (K) channel. The derived Drosophila and rat eag polypeptides share > 670 amino acids, with a sequence identity of 61%, exhibiting a high degree of similarity at the N-terminus, the hydrophobic core including the pore forming P region and a potential cyclic nucleotide binding site. Rat eag mRNA is specifically expressed in the central nervous system. In the Xenopus oocyte expression system rat eag mRNA gives rise to voltage activated K channels which have distinct properties in comparison with Drosophila eag channels and other voltage activated K channels. Thus, the rat eag channel further extends the known diversity of K channels. Most notably, the kinetics of rat eag channel activation depend strongly on holding membrane potential. Hyperpolarization slows down the kinetics of activation; conversely depolarization accelerates the kinetics of activation. This novel K channel property may have important implications in neural signal transduction allowing neurons to tune their repolarizing properties in response to membrane hyperpolarization.
Asunto(s)
Canales de Potasio/fisiología , Secuencia de Aminoácidos , Animales , Secuencia de Bases , ADN Complementario , Drosophila , Proteínas de Drosophila , Canales de Potasio Éter-A-Go-Go , Activación del Canal Iónico/fisiología , Masculino , Datos de Secuencia Molecular , Proteínas del Tejido Nervioso/fisiología , Oocitos/metabolismo , Reacción en Cadena de la Polimerasa , Canales de Potasio/biosíntesis , Canales de Potasio/química , ARN Mensajero/análisis , Ratas , Ratas Sprague-Dawley , Proteínas Recombinantes/biosíntesis , Homología de Secuencia de Aminoácido , Especificidad de la Especie , Xenopus laevisRESUMEN
Structural and functional diversity of voltage-gated Kv1-type potassium channels in rat brain is enhanced by the association of two different types of subunits, the membrane-bound, poreforming alpha-subunits and a peripheral beta-subunit. We have cloned a beta-subunit (Kv beta 1) that is specifically expressed in the rat nervous system. Association of Kv beta 1 with alpha-subunits confers rapid A-type inactivation on non-inactivating Kv1 channels (delayed rectifiers) in expression systems in vitro. This effect is mediated by an inactivating ball domain in the Kv beta 1 amino terminus.
Asunto(s)
Canales de Potasio/química , Canales de Potasio/fisiología , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Encéfalo/metabolismo , Bovinos , Clonación Molecular , Técnicas In Vitro , Activación del Canal Iónico , Subunidades beta de los Canales de Potasio de Gran Conductancia Activados por el Calcio , Potenciales de la Membrana/fisiología , Datos de Secuencia Molecular , Oocitos/fisiología , Fragmentos de Péptidos , ARN Mensajero/biosíntesis , Ratas , Homología de Secuencia de Aminoácido , Xenopus laevisRESUMEN
Previously, we characterized a Shaker-related family of voltage-gated potassium channels (RCK) in rat brain. Now, we describe a second family of voltage-gated potassium channels in the rat nervous system. This family is related to the Drosophila Shaw gene and has been dubbed Raw. In contrast to the RCK potassium channel family the Raw family utilizes extensive alternative splicing for expressing potassium channel subunits with variant C-termini. These alternative C-termini do not appear to influence the electrophysiological and pharmacological properties as studied in the Xenopus oocyte expression system. In situ hybridizations to sections of rat brain indicate that members of the Raw family are expressed in distinct areas of the central nervous system. Probably, Raw channels are expressed predominantly as homomultimers. Immunocytochemical experiments with antibodies against Raw3 and RCK4 proteins which form two distinct A-type potassium channels indicate that in hippocampus the two channels are expressed both in different neurons and in the same ones. In general, properties of Raw potassium channels appeared to be similar to RCK channels. However, Raw outward currents, in contrast to RCK currents, exhibit an intense rectification at test potentials higher than +20 to +40 mV. RCK and Raw channel subunits did not measurably coassemble into RCK/Raw heteromultimers after coinjecting RCK and Raw cRNA into Xenopus oocytes. These results suggest that members of the RCK and the Raw potassium channel families express potassium channels which form independent outward current systems. Combining the results of in situ hybridizations, immunocytochemical staining and expression of the cloned potassium channels in Xenopus oocytes demonstrates that unrestrained mixing of potassium channel subunits to form hybrid channels does not occur in the rat central nervous system. A single neuron is able to express multiple, independently assembled potassium channels.
Asunto(s)
Encéfalo/metabolismo , Proteínas de Drosophila , Hormonas de Insectos/genética , Proteínas del Tejido Nervioso/genética , Canales de Potasio/genética , Secuencia de Aminoácidos , Animales , Autorradiografía , Secuencia de Bases , Northern Blotting , ADN , Inmunohistoquímica , Hormonas de Insectos/metabolismo , Activación del Canal Iónico , Potenciales de la Membrana , Datos de Secuencia Molecular , Hibridación de Ácido Nucleico , Canales de Potasio/metabolismo , ARN/metabolismo , Ratas , Ratas Endogámicas , Alineación de Secuencia , Canales de Potasio Shaw , Xenopus laevisRESUMEN
A rat brain cDNA (Raw3) related to the Drosophila Shaw K+ channel family has been characterized. Raw3 cRNA leads to the formation of TEA-insensitive, fast inactivating (A-type) K+ channels when injected into Xenopus laevis oocytes. Raw3 channels have markedly different properties from the previously cloned rat A-type K+ channel RCK4, Raw3 channels operate in the positive voltage range.