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1.
JGH Open ; 7(9): 610-617, 2023 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-37744709

RESUMEN

Background and Aim: Stimulant laxatives may cause electrolyte abnormalities, dehydration, and abdominal pain; their long-term use can lead to tolerance and subsequent refractory constipation. We investigated the effectiveness, safety, and quality of life after switching from stimulant laxatives to lubiprostone in elderly patients with chronic constipation (CC). Methods: This multicenter, interventional, open-label, single-arm, before-and-after comparison study enrolled 99 Japanese patients aged 65-90 years with CC who took stimulant laxatives for ≥2 weeks prior to switching to lubiprostone monotherapy. Results: The mean ± SD spontaneous defecations at Week 1 of 7.8 ± 6.2 times/week was not significantly different from that at baseline (8.3 ± 4.7). Spontaneous defecations were significantly reduced at Weeks 2 (-1.5 ± 4.0, P < 0.001) and 4 (-1.5 ± 3.7, P < 0.001). The Bristol Stool Form Scale score did not change from baseline (4.7 ± 0.9) at Weeks 1 (4.5 ± 1.3) or 4 (4.3 ± 1.3), but it did at Week 2 (4.3 ± 1.5, P < 0.05). The Patient Assessment of Constipation Quality of Life questionnaire score increased (0.36 ± 0.07, P < 0.001) after 28 days. Nausea was the only symptom that worsened from baseline and was the most frequently reported adverse drug reaction (15.2%). Conclusion: Switching to lubiprostone monotherapy for CC was not associated with significant concerns in short-term spontaneous defecation frequency and safety, but it might affect the efficacy and patient quality of life over 2 weeks. Careful treatment strategies facilitating gradual switching to lubiprostone monotherapy may be needed in patients using stimulant laxatives.

2.
J Neurosurg Pediatr ; 18(2): 183-6, 2016 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-27058456

RESUMEN

Lumbo-costo-vertebral syndrome (LCVS) is a rare disorder in children that is characterized by hemivertebrae, congenital absence of ribs, meningocele, and hypoplasia of the truncal and abdominal wall presenting as a congenital lumbar hernia. An otherwise healthy 12-month-old girl was referred to the authors' hospital with soft swelling on her left middle back; scoliosis had been present since birth. Imaging revealed a thoracic meningocele, ectopia of the spleen suggesting lumbar hernia, multiple anomalies of the thoracic vertebral columns, and defects of the ribs; thus, LCVS was diagnosed. Surgical observation revealed that the meningocele was firmly anchored to part of the diaphragm, which created stretching tension in the meningocele continuously with exhalation. Once detached, the meningocele shrank spontaneously and never developed again after cauterization. In this case, continuous or pulsatile pressure in the presence of a vertebral defect was thus considered to be an important factor for formation of the thoracic meningocele.


Asunto(s)
Anomalías Múltiples/diagnóstico por imagen , Diafragma/diagnóstico por imagen , Vértebras Lumbares/diagnóstico por imagen , Meningocele/diagnóstico por imagen , Vértebras Torácicas/diagnóstico por imagen , Anomalías Múltiples/cirugía , Preescolar , Diafragma/cirugía , Femenino , Humanos , Vértebras Lumbares/cirugía , Imagen por Resonancia Magnética , Meningocele/cirugía , Vértebras Torácicas/cirugía
3.
FEBS Lett ; 580(15): 3721-5, 2006 Jun 26.
Artículo en Inglés | MEDLINE | ID: mdl-16765953

RESUMEN

Tunicamycin is a well-known inhibitor of protein glycosylation and used as an inducer of endoplasmic reticulum (ER) stress. We found that tunicamycin induced expression of cytochrome P450 1A1 in a dose-dependent manner. Like dioxin, the transcriptional induction was associated with dose-dependent activation of the dioxin responsive element (DRE). This effect was independent of inhibition of protein glycosylation or induction of ER stress. Pharmacological and genetic inhibition of the aryl hydrocarbon receptor (AhR) significantly attenuated activation of DRE by tunicamycin. These results elucidated the novel potential of tunicamycin as an activator of the AhR -- DRE signaling pathway.


Asunto(s)
Dioxinas/farmacología , Regulación de la Expresión Génica/efectos de los fármacos , Receptores de Hidrocarburo de Aril/metabolismo , Elementos de Respuesta/genética , Transducción de Señal/efectos de los fármacos , Tunicamicina/farmacología , Animales , Línea Celular Tumoral , Citocromo P-450 CYP1A1/genética , Retículo Endoplásmico/efectos de los fármacos , Retículo Endoplásmico/metabolismo , Glicosilación , Ratones , ARN Mensajero/genética , Receptores de Hidrocarburo de Aril/agonistas
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