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1.
National Journal of Andrology ; (12): 832-834, 2011.
Artículo en Chino | WPRIM | ID: wpr-305779

RESUMEN

<p><b>OBJECTIVE</b>To evaluate the effect of endourethrotomy with thulium laser as a minimally invasive treatment for urethral stricture.</p><p><b>METHODS</b>We treated 36 cases of urethral stricture or atresia by endourethrotomy with thulium laser, restored the urethral continuity by vaporization excision of the scar tissue, and observed the clinical effects and complications.</p><p><b>RESULTS</b>The mean operation time was 35 min, ranging from 10 to 90 min. Smooth urination was achieved after 2-6 weeks of catheter indwelling, with no urinary incontinence. The patients were followed up for 4-24 (mean 12) months, during which 27 did not need any reintervention, 5 developed urinary thinning but cured by urethral dilation, 3 received another laser urethrotomy for previous negligence of timely urethral dilation, and the other 1 underwent open urethroplasty.</p><p><b>CONCLUSION</b>Thulium laser urethrotomy is a safe and effective minimally invasive option for short urethral stricture, which is also suitable for severe urethral stricture and urethral atresia. Its short-term outcome is satisfactory, but its long-term effect remains to be further observed.</p>


Asunto(s)
Adulto , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Terapia por Láser , Tulio , Usos Terapéuticos , Resultado del Tratamiento , Ureteroscopía , Estrechez Uretral , Cirugía General
2.
China Journal of Chinese Materia Medica ; (24): 797-800, 2006.
Artículo en Chino | WPRIM | ID: wpr-351792

RESUMEN

<p><b>OBJECTIVE</b>To provide scientific basis for large scale production by studying the technique of tissue culture of Gentiana stramines.</p><p><b>METHOD</b>Callus was induced from germ-free stem segment of G. stramines on a MS medium supplemented with different hormones.</p><p><b>RESULT</b>The MS medium with 0.5-1.0 mg x L(-1) BA and 0.5 mg x L(-1) NAA was suitable for the induction and proliferation of cluster bads. MS medium with 1.0 mg x L(-1) IAA and 3 mg x L(-1) BA was suitable for the induction of calli. MS medium with 1.0 mg x L(-1) IAA and 2.0-3.0 mg x L(-1) BA was suitable for the subculture of calli. MS medium with 2.0 mg x L(-1) BA and 0.5 mg x L(-1) NAA was suitable for the differentiation of calli.</p><p><b>CONCLUSION</b>Aseptic seeding of G. stramines can be quickly propagated by shoot culture.</p>


Asunto(s)
Medios de Cultivo , Gentiana , Reguladores del Crecimiento de las Plantas , Farmacología , Tallos de la Planta , Plantas Medicinales , Regeneración , Plantones , Técnicas de Cultivo de Tejidos , Métodos
3.
China Journal of Chinese Materia Medica ; (24): 313-316, 2003.
Artículo en Chino | WPRIM | ID: wpr-282180

RESUMEN

<p><b>OBJECTIVE</b>To amplify the PCR with the internal transcribed spacerl regions measure the base sequence of the amplified products of DNA, and to set up an identified standard on the level of molecule.</p><p><b>METHOD</b>DNA from the seeds of G. dahurica was extracted by conventional method, and composed peculiar primer was used to amplify with the internal transcribed spacerl regions of the rRNA gene, and the base sequence of the amplified products by stopping the circle of the end of double deoxidation of four color fluorescent mark was measured.</p><p><b>RESULT</b>It was proved by agar sugar gel electrophoresis that the PCR amplified products of the internal transcribed spacerl regions of the rRNA gene existed. The base sequence of the seeds of G. dahurica's internal transcribed spacerl regions of the rRNA gene was measured.</p><p><b>CONCLUSION</b>To measure the base sequence of internal transcribed spacerl regions of the rRNA gene in the seeds of G. dahurica's is a method to identify vegetal Chinese traditional medicine on the level of molecule.</p>


Asunto(s)
Secuencia de Bases , ADN de Plantas , Genética , ADN Espaciador Ribosómico , Genética , Gentiana , Genética , Datos de Secuencia Molecular , Plantas Medicinales , Genética , Reacción en Cadena de la Polimerasa , ARN Ribosómico , Genética , Semillas , Genética
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