RESUMO
FPA is a gene that regulates flowering time in Arabidopsis via a pathway that is independent of daylength (the autonomous pathway). Mutations in FPA result in extremely delayed flowering. FPA was identified by means of positional cloning. The predicted FPA protein contains three RNA recognition motifs in the N-terminal region. FPA is expressed most strongly in developing tissues, similar to the expression of FCA and LUMINIDEPENDENS, two components of the autonomous pathway previously identified. Overexpression of FPA in Arabidopsis causes early flowering in noninductive short days and creates plants that exhibit a more day-neutral flowering behavior.
Assuntos
Proteínas de Arabidopsis , Arabidopsis/genética , Genes de Plantas , Proteínas de Plantas/genética , Proteínas de Ligação a RNA/genética , Alelos , Motivos de Aminoácidos , Sequência de Aminoácidos , Animais , Arabidopsis/crescimento & desenvolvimento , Clonagem Molecular , Expressão Gênica , Humanos , Dados de Sequência Molecular , Proteínas de Plantas/metabolismo , Proteínas de Plantas/fisiologia , RNA de Plantas/metabolismo , Proteínas de Ligação a RNA/metabolismo , Proteínas de Ligação a RNA/fisiologia , Homologia de Sequência de AminoácidosRESUMO
The gibberellin (GA) 20-oxidase encoded by Arabidopsis GA5 catalyzes the synthesis of active GAs. GA5 is a regulatory step in GA biosynthesis as GA5 mRNA levels are negatively regulated by its bioactive GA products. A fusion between the GA5 promoter and the firefly luciferase reporter (GA5-LUC) was shown to be similarly regulated, indicating GA feedback of GA5 occurs at the transcriptional level. The fidelity of the GA5-LUC reporter permitted a fusion genetic screen to identify mutants altered in transgene expression. This bioimaging screen identified two types of recessive mutants with increased LUC activity and apparent GA-related growth phenotypes, a dwarf (lue1) and two late flowering mutants (fpa1-3 and fpa1-4). Mutant progeny exhibited altered levels of LUC and of endogenous GA5 and other GA-regulated mRNAs. SSLP-based mapping localized lue1 to chromosome I near the ga2 locus, although complementation analyzes showed that lue1 is not allelic to ga2. Mapping and complementation analyzes showed that the late flowering mutants are allelic to fpa1. This provides genetic evidence for crosstalk between the autonomous and gibberellin-dependent flowering pathways.
Assuntos
Arabidopsis/genética , Regulação da Expressão Gênica de Plantas , Giberelinas/metabolismo , Oxigenases de Função Mista/genética , Arabidopsis/metabolismo , Arabidopsis/fisiologia , Mapeamento Cromossômico , Genes Reporter , Teste de Complementação Genética , Giberelinas/biossíntese , Glucuronidase/metabolismo , Luciferases/genética , Luciferases/metabolismo , Oxigenases de Função Mista/metabolismo , Dados de Sequência Molecular , Mutação , Fenótipo , Plantas Geneticamente Modificadas , Polimorfismo Conformacional de Fita Simples , Proteínas Recombinantes de Fusão/genética , Proteínas Recombinantes de Fusão/metabolismoRESUMO
In light of evidence suggesting the proinflammatory and nociceptive action of peripheral serotonin (5-HT), the present study examined dose-dependent parameters of edema and algesia produced by intraplantar injections of 5-HT and the role of heterogeneous 5-HT receptors in these 5-HT-induced responses. Intraplantar 5-HT (0.05, 0.25, 0.5, or 1.0 mumols) produced paw edema at each 5-HT concentration and produced concentration-dependent increases in the nociceptive response as indexed by lifts of, and licks to the affected paw. Intraplantar pretreatment with the 5-HT1 receptor antagonist methysergide at concentrations greater than or equal to 3 nmol attenuated the 5-HT-induced (25 mumols) inflammatory and nociceptive responses. At concentrations greater than or equal to 300 nmol, both 5-HT2 receptor antagonist ketanserin and 5-HT3 receptor antagonist odansetron pretreatment blocked 5-HT-induced inflammatory and nociceptive responses. These results more completely define peripheral 5-HT-receptor-dependent systems of 5-HT-induced inflammation and nociception in rats.
Assuntos
Inflamação/fisiopatologia , Dor/fisiopatologia , Receptores de Serotonina/fisiologia , Serotonina/farmacologia , Animais , Comportamento Animal/efeitos dos fármacos , Relação Dose-Resposta a Droga , Imidazóis/farmacologia , Inflamação/induzido quimicamente , Ketanserina/farmacologia , Masculino , Metisergida/farmacologia , Ondansetron , Dor/induzido quimicamente , Ratos , Ratos Endogâmicos , Receptores de Serotonina/efeitos dos fármacos , Antagonistas da Serotonina/farmacologiaRESUMO
This study was designed to evaluate the transcutaneous electrical nerve stimulation (TENS) postoperative program administered by a physical therapy department. A surgeon, a physical therapist, a recovery room nurse, and unit nurses participated in the program which included preoperative evaluation and patient education, application of sterile electrodes parallel to the incision in the operating room, TENS activation in the recovery room, follow-up visits, and data collection. Seventy-five patients who underwent laparotomy and received TENS at the most comfortable machine settings were compared by chart review to 75 patients who had undergone similar surgical procedures performed by the same surgeon before TENS postoperative pain management had been instituted. The TENS was applied for an average of five days; machine settings of intensity, frequency, and pulse width tended to be midrange. The TENS group took significantly less pain medication, but the length of hospital stay was not significantly different. Patients with TENS rated their pain on 10-point scales as more intense than uncomfortable. This study demonstrated that a well-structured interdisciplinary program of postoperative TENS management can reduce the amount of pain medication taken by patients after laparotomy.
Assuntos
Terapia por Estimulação Elétrica , Dor Pós-Operatória/terapia , Abdome/cirurgia , Colecistectomia , Gastrectomia , Hérnia Ventral/cirurgia , Humanos , Pancreatectomia , Serviço Hospitalar de FisioterapiaRESUMO
Thirty patients with symptomatic rheumatoid arthritis (RA) of both hands were treated with an air pressure splint. Evaluations were made by measuring ring size, hand volume, range and rate of finger motions, grip strength and degree of pain and stiffness. One hand was randomly assigned to the treatment group while the other served as a control. Patients received the air splint treatment for 5 consecutive days. Data were analyzed by a 2-factor repeated analysis of variance to determine the effectiveness of 1 treatment, the cumulative effect of 5 treatments, the effect of the 5th treatment, and whether the results after the 1st treatment lasted until the 5th treatment. All measurements except hand volume significantly improved with the 1st treatment. Furthermore, the beneficial effects persisted throughout the treatment period. These data indicate the air splint treatment is effective in reducing swelling and other symptoms of RA in the hands.