RESUMEN
The ingestion of scarlet pimpernel (Lysimachia arvensis L.), also known as red chickweed, has been reported as a cause of death of cattle in Uruguay, and as the suspected cause of deaths of sheep in Australia. It has not previously been reported in association with deaths of cattle in Australia. We report the clinical and pathological findings from four cattle in western Victoria that died with a nephrosis suspected to be secondary to intoxication with scarlet pimpernel.
Asunto(s)
Anagallis/envenenamiento , Enfermedades de los Bovinos/patología , Nefrosis/veterinaria , Intoxicación por Plantas/veterinaria , Animales , Australia , Bovinos , Enfermedades de los Bovinos/etiología , Brotes de Enfermedades/veterinaria , Nefrosis/etiología , Nefrosis/patología , Intoxicación por Plantas/complicaciones , Intoxicación por Plantas/patología , Ovinos , Enfermedades de las Ovejas/etiología , Enfermedades de las Ovejas/patología , Especificidad de la EspecieAsunto(s)
Apolipoproteínas/genética , Diabetes Mellitus Tipo 2/genética , Lipoproteínas LDL/metabolismo , Polimorfismo de Nucleótido Simple/genética , Apolipoproteína A-V , Apolipoproteínas A , Apolipoproteínas E/genética , Colesterol/sangre , Diabetes Mellitus Tipo 2/sangre , Diabetes Mellitus Tipo 2/metabolismo , Frecuencia de los Genes , Genotipo , Humanos , Lipoproteína Lipasa/sangre , Lipoproteínas/sangre , Lipoproteínas LDL/química , Lipoproteínas LDL/aislamiento & purificación , Tamaño de la Partícula , Triglicéridos/sangreRESUMEN
The aminoalkylindoles (AAIs) are agonists at both the cannabinoid CB1 and CB2 receptors. To determine whether the s-trans or s-cis form of AAIs is their receptor-appropriate conformation, two pairs of rigid AAI analogues were studied. These rigid analogues are naphthylidene-substituted aminoalkylindenes that lack the carbonyl oxygen of the AAIs. Two pairs of (E)- and (Z)-naphthylidene indenes (C-2 H and C-2 Me) were considered. In each pair, the E geometric isomer is intended to mimic the s-trans form of the AAIs, while the Z geometric isomer is intended to mimic the s-cis form. Complete conformational analyses of two AAIs, pravadoline (2) and WIN-55, 212-2 (1), and of each indene were performed using the semiempirical method AM1. S-trans and s-cis conformations of 1 and 2 were identified. AM1 single-point energy calculations revealed that when 1 and each indene were overlayed at their corresponding indole/indene rings, the (E)- and (Z)-indenes were able to overlay naphthyl rings with the corresponding s-trans or s-cis conformer of 1 with an energy expense of 1.13/0.69 kcal/mol for the C-2 H (E/Z)-indenes and 0.82/0.74 kcal/mol for the C-2 Me (E/Z)-indenes. On the basis of the hypothesis that aromatic stacking is the predominant interaction of AAIs such as 1 at the CB receptors and on the demonstration that the C-2 H (E/Z)- and C-2 Me (E/Z)-indene isomers can mimic the positions of the aromatic systems in the s-trans and s-cis conformers of 1, the modeling results support the previously established use of indenes as rigid analogues of the AAIs. A synthesis of the naphthylidene indenes was developed using Horner-Wittig chemistry that afforded the Z isomer in the C-2 H series, which was not produced in significant amounts from an earlier reported indene/aldehyde condensation reaction. This approach was extended to the C-2 Me series as well. Photochemical interconversions in both the C-2 H and C-2 Me series were also successful in obtaining the less favored isomer. Thus, the photochemical process can be used to provide quantities of the minor isomers C-2 H/Z and C-2 Me/E. The CB1 and CB2 affinities as well as the activity of each compound in the twitch response of the guinea pig ileum (GPI) assay were assessed. The E isomer in each series was found to have the higher affinity for both the CB1 and CB2 receptors. In the rat brain membrane assay versus [3H]CP-55,940, the Ki's for the C-2 H/C-2 Me series were 2.72/2.89 nM (E isomer) and 148/1945 nM (Z isomer). In membrane assays versus [3H]SR141716A, a two-site model was indicated for the C-2 H/C-2 Me (E isomers) with Ki's of 10. 8/9.44 nM for the higher-affinity site and 611/602 nM for the lower-affinity site. For the Z isomers, a one-site model was indicated with Ki's of 928/2178 nM obtained for the C2 H/C-2 Me analogues, respectively. For the C-2 H/C-2 Me series, the CB2 Ki's obtained using a cloned cell line were 2.72/2.05 nM (E isomer) and 132/658 nM (Z isomer). In the GPI assay, the relative order of potency was C-2 H E > C-2 Me E > C-2 H Z > C-2 Me Z. The C-2 H E isomer was found to be equipotent with 1, while the C-2 Me Z isomer was inactive at concentrations up to 3.16 microM. Thus, results indicate that the E geometric isomer in each pair of analogues is the isomer with the higher CB1 and CB2 affinities and the higher pharmacological potency. Taken together, results reported here support the hypothesis that the s-trans conformation of AAIs such as 1 is the preferred conformation for interaction at both the CB1 and CB2 receptors and that aromatic stacking may be an important interaction for AAIs at these receptors.
Asunto(s)
Cannabinoides/metabolismo , Indenos/metabolismo , Morfolinas/metabolismo , Naftalenos/metabolismo , Receptor Cannabinoide CB2 , Receptores de Droga/metabolismo , Animales , Benzoxazinas , Unión Competitiva , Células CHO , Cricetinae , Cobayas , Íleon/efectos de los fármacos , Íleon/inervación , Íleon/fisiología , Técnicas In Vitro , Indenos/química , Indoles/química , Ligandos , Modelos Moleculares , Conformación Molecular , Morfolinas/química , Contracción Muscular/efectos de los fármacos , Músculo Liso/efectos de los fármacos , Músculo Liso/inervación , Plexo Mientérico/efectos de los fármacos , Plexo Mientérico/fisiología , Naftalenos/química , Ratas , Receptores de Cannabinoides , Receptores de Droga/agonistas , EstereoisomerismoRESUMEN
To further characterize neuronal cannabinoid receptors, we compared the ability of known and novel cannabinoid analogs to compete for receptor sites labeled with either [3H]SR141716A or [3H]CP-55,940. These efforts were also directed toward extending the structure-activity relationships for cannabinoid agonists and antagonists. A series of alternatively halogenated analogs of SR141716A were synthesized and tested in rat brain membrane binding assays along with the classical cannabinoids, Delta9-tetrahydrocannabinol, cannabinol, cannabidiol, the nonclassical cannabinoid CP-55,940, the aminoalkylindole WIN55212-2 and the endogenous fatty acid ethanolamide, anandamide. Saturation binding isotherms were performed with both radioligands, as were displacement studies, allowing an accurate comparison to be made between the binding of these various compounds. Competition studies demonstrated that all of the compounds were able to displace the binding of [3H]CP-55,940 with rank order potencies that agreed with previous studies. However, the rank order potencies of these compounds in competition studies with [3H]SR141716A differed significantly from those determined with [3H]CP-55,940. These results suggest that CP-55,940, WIN55212-2 and other agonists interact with cannabinoid binding sites within the brain which are distinguishable from the population of binding sites for SR141716A, its analogs and cannabidiol. Structural modification of SR141716A significantly altered the affinity of the compound and its relative ability to displace either [3H]CP-55,940 or [3H]SR141716A preferentially within the rat brain receptor membrane preparation.
Asunto(s)
Analgésicos/metabolismo , Cannabinoides/agonistas , Cannabinoides/antagonistas & inhibidores , Ciclohexanoles/metabolismo , Piperidinas/metabolismo , Pirazoles/metabolismo , Analgésicos/farmacología , Animales , Unión Competitiva/efectos de los fármacos , Ciclohexanoles/farmacología , Masculino , Modelos Moleculares , Piperidinas/farmacología , Pirazoles/farmacología , Ratas , Ratas Endogámicas F344 , RimonabantAsunto(s)
Rinorrea de Líquido Cefalorraquídeo/etiología , Síndrome de Silla Turca Vacía/complicaciones , Rinorrea de Líquido Cefalorraquídeo/diagnóstico , Rinorrea de Líquido Cefalorraquídeo/cirugía , Síndrome de Silla Turca Vacía/diagnóstico , Síndrome de Silla Turca Vacía/cirugía , Femenino , Humanos , Persona de Mediana EdadRESUMEN
Injection of glucocorticoid hormone to adrenalectomized rats induces in liver microsomes a factor which stimulates polypeptide synthesis in a cell-free system. The factor is extractable from microsomes by 0.5 M KC1 followed by gel filtration, of the extract. Induction of the activator in glucocorticoid-treated rats contribute higher protein-synthesizing ability of the microsomes following hormone administration.
Asunto(s)
Microsomas Hepáticos/metabolismo , Prednisolona/farmacología , Biosíntesis de Proteínas , Animales , Masculino , Factores de Iniciación de Péptidos , Ratas , Estimulación QuímicaRESUMEN
Four methods are described to obtain pure neuronal cultures from chick embryo cerebral hemispheres. In our experimental conditions the proliferation of the glial cells in inhibited and cultures of either low or high neuronal density are obtained. The isolated neurons, however, did not survive longer than 8 to 10 days; the contact with glial cells seems to be necessary for the maintenance of the neurons in long-term cultures.