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1.
Endoscopy ; 41(11): 923-8, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19802773

RESUMO

BACKGROUND AND AIM: Endoscopic submucosal dissection (ESD) is feasible as a treatment for early gastric cancer (EGC) when it is performed by an experienced endoscopist. We investigated whether it was feasible for novice endoscopists to perform ESD for EGC, and how difficult it was to learn the procedure. METHODS: This case series study was performed in a cancer referral center. Three resident endoscopists, who had already learned basic procedures, performed ESD under supervision for 30 consecutive lesions, and their procedures were analyzed. The procedure was divided for assessment into (i) mucosal incision and (ii) submucosal dissection by completion of the circumferential mucosal cut. An insulated-tip knife was used for mucosal incision and submucosal dissection. A total of 90 mucosal EGCs (< or = 2 cm) without ulcers or scars in 87 patients were included. Outcomes were: rates of complete resection, complications, and self-completion; operation time; learning curve; and reasons for change of supervisor as an indicator of difficulty. RESULTS: Among the 90 procedures, there was a good overall complete resection rate of 93 %, with an acceptable complication rate of 4.4 %; the complications were delayed hemorrhage in two patients, and perforations in another two patients that were repaired successfully by endoscopic clipping. The self-completion rate and operation time were significantly worse for submucosal dissection than for mucosal incision. Two of the three operators showed a flat learning curve for submucosal dissection. Difficulty with the procedure was related mainly to uncontrollable hemorrhage. CONCLUSIONS: With appropriate supervision, gastric ESD by residents is feasible, with equivalent complete resection rates and acceptable complication rates compared with those of experienced endoscopists, although there was difficulty in achieving sufficient self-completion rates in submucosal dissection. Better control of bleeding during submucosal dissection may be a key to improving the procedure.


Assuntos
Dissecação/métodos , Mucosa Gástrica/cirurgia , Internato e Residência , Neoplasias Gástricas/cirurgia , Idoso , Estudos de Viabilidade , Gastroscopia , Humanos , Masculino
2.
Int J Urol ; 4(2): 191-7, 1997 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-9179695

RESUMO

BACKGROUND: Non-adrenergic, non-cholinergic (NANC) relaxation evoked by electrical field stimulation (EFS) has been observed in the urethra, with nitric oxide (NO) considered the agent most probably mediating this effect. However, Burnstock's purinergic hypothesis suggests that ATP and related purine compounds are neurotransmitters in NANC relaxation, although the physiological and pharmacological effects of ATP and related purine compounds in the urethra have been little studied. METHODS: The effects of ATP and related purine compounds, NG-nitro-L-arginine (NOARG; an inhibitor of nitric oxide synthesis from L-arginine), calcitonin gene-related peptide (CGRP), substance P and vasoactive intestinal polypeptide (VIP) on relaxation and smooth muscle tension induced by electrical field stimulation (EFS) were studied in isolated male rabbit circular urethral smooth muscle (functional study). In addition, the outflow of ATP elicited by EFS was measured using the luciferase technique (superfusion study). All experiments were performed in the presence of guanethidine (3 x 10(-3) mol/L) and atropine (10(-6) mol/L). RESULTS: In preparations contracted with U46619, a prostaglandin peroxidase inhibitor, ATP had almost no effect on EFS-induced relaxation; however, suramin, a non-selective P2Y-purinoceptor antagonist, and NOARG each markedly attenuated this relaxation in a concentration-dependent manner. ATP and related purine compounds (adenosine, AMP and ADP) each reduced U46619-induced tonic contraction in a concentration-dependent manner. The potencies of the relaxant effects of ATP and these purine compounds were almost the same. In preparations contracted with U46619, CGRP and substance P had no effect on tonic contraction, but VIP reduced tonic contraction in a concentration-dependent manner. In the superfusion study, the outflow of ATP into the superfusate was markedly increased by EFS. When NOARG or prazosin was added to the superfusate, the increase in outflow of ATP was unchanged, but when suramin was added to the superfusate, no increase in outflow of ATP was observed. CONCLUSIONS: These findings suggest that P2Y-purinoceptors exist in the male rabbit urethra, and that ATP and related purine compounds may play a role in non-adrenergic, non-cholinergic neurotransmission. Consequently, the pathways mediating urethral relaxation by ATP, NO and VIP may be different.


Assuntos
Trifosfato de Adenosina/fisiologia , Relaxamento Muscular/fisiologia , Purinas/metabolismo , Uretra/fisiologia , Trifosfato de Adenosina/metabolismo , Trifosfato de Adenosina/farmacologia , Animais , Estimulação Elétrica , Técnicas In Vitro , Masculino , Neuropeptídeos/farmacologia , Perfusão , Purinas/farmacologia , Coelhos , Uretra/efeitos dos fármacos , Uretra/metabolismo
3.
Nucleic Acids Symp Ser ; (37): 5-6, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9585971

RESUMO

Novel dioxane nucleosides having two bases, 2(R)-(5-fluorouracil-1-yl)-5(R)-hydroxymethyl-3(R)-(uracil-1-yl)-1,4-dioxane (7a) and 2(S)-(5-fluorouracil-1-yl)-5(R)-hydroxymethyl-3(R)-(uracil-1-yl)-1,4-dioxane (7b) were synthesized from uridine to develop a new category of nucleoside for therapeutic use. Some derivative of precursors of the nucleoside were also synthesized and several compounds synthesized were tested antitumor activity using human gastric cancer cell lines in culture.


Assuntos
Antimetabólitos Antineoplásicos/síntese química , Dioxanos/síntese química , Fluoruracila/análogos & derivados , Antimetabólitos Antineoplásicos/química , Antimetabólitos Antineoplásicos/toxicidade , Dioxanos/química , Dioxanos/toxicidade , Fluoruracila/síntese química , Fluoruracila/química , Fluoruracila/toxicidade , Humanos , Indicadores e Reagentes , Estrutura Molecular , Neoplasias Gástricas , Células Tumorais Cultivadas , Uridina
4.
Jpn J Pharmacol ; 59(3): 333-8, 1992 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-1279255

RESUMO

The relaxant effects of calcitonin gene-related peptide (CGRP) and other drugs were compared in basilar artery rings obtained from stroke-prone spontaneously hypertensive rats (SHRSP) and Wistar-Kyoto rats (WKY). In addition, the relaxant effect of CGRP on basilar arteries from spontaneously hypertensive rats (SHR) was examined. Relaxation induced by CGRP was independent of the presence of endothelium, and it was markedly increased in SHRSP when compared to WKY. In contrast, acetylcholine-induced relaxation was endothelium-dependent and did not differ between the two groups. Enhanced CGRP-induced relaxation was also found in SHR when compared to WKY. However, the relaxant response was greater in SHRSP than in SHR. No significant differences were found in the relaxation induced by isoproterenol, forskolin, dibutyryl cyclic AMP, and 3-isobutyl-1-methylxanthine in endothelium-rubbed arteries of WKY and SHRSP. These results suggest that CGRP produces endothelium-independent relaxation in the rat basilar artery, and that the enhanced CGRP-induced relaxation found in SHRSP may not be associated with alterations of vasodilation mediated by cyclic AMP.


Assuntos
Artéria Basilar/efeitos dos fármacos , Peptídeo Relacionado com Gene de Calcitonina/farmacologia , Hipertensão/fisiopatologia , Vasodilatação/efeitos dos fármacos , 1-Metil-3-Isobutilxantina/farmacologia , Acetilcolina/farmacologia , Animais , Bucladesina/farmacologia , Colforsina/farmacologia , Técnicas In Vitro , Isoproterenol/farmacologia , Masculino , Ratos , Ratos Endogâmicos SHR , Ratos Endogâmicos WKY
5.
J Toxicol Sci ; 3(4): 313-23, 1978 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-216817

RESUMO

A possible mechanism of infertility by Cd was investigated from the standpoint of influence of Cd on the contractile responses of isolated seminal vesicle from guinea pigs to K, acetylcholine, noradrenaline, Ba and Ca by using the Magnus method. Cd inhibited the contractile responses to the contractile agents tested in a dose-dependent manner. Cd showed the preferential inhibition against the contractile responses to K and Ca. The inhibitory effect of Cd on the contractile responses to noradrenaline and acetylcholine was hardly removed. The effect of Cd was inhibited by the thiol compounds, glutathione and thiola. The active mechanism of Cd was discussed in relation to Ca mobilization.


Assuntos
Cádmio/farmacologia , Contração Muscular/efeitos dos fármacos , Músculo Liso/efeitos dos fármacos , Glândulas Seminais/efeitos dos fármacos , Acetilcolina/farmacologia , Animais , Bário/farmacologia , Intoxicação por Cádmio/complicações , Cálcio/farmacologia , Interações Medicamentosas , Cobaias , Técnicas In Vitro , Infertilidade Masculina/induzido quimicamente , Masculino , Norepinefrina/farmacologia , Potássio/farmacologia , Compostos de Sulfidrila/farmacologia , Fatores de Tempo
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