ATS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Takashi Tojo
Shigeki Taniguchi
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kushibe, K.
Right arrow Articles by Taniguchi, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kushibe, K.
Right arrow Articles by Taniguchi, S.

Ann Thorac Surg 2000;70:1876-1879
© 2000 The Society of Thoracic Surgeons


Original article: general thoracic

Effects of warm ischemia and cryopreservation on cartilage viability of tracheal allografts

Keiji Kushibe, MDa, Takashi Tojo, MDa, Hidehito Sakaguchi, MDa, Makoto Takahama, MDa, Kazuhiko Nishizaki, MDa, Kunimoto Nezu, MDa, Shigeki Taniguchi, MDa

a Department of Surgery III, Nara Medical University, Nara, Japan

Accepted for publication May 5, 2000.

Address reprint requests to Dr Kushibe, Department of Surgery III, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan, 634-8522
e-mail: kushikuk{at}nmu-gw.naramed-u.ac.jp

Background. For clinical use of a cryopreserved tracheal allograft, it is important to evaluate cartilage viability. We assessed cell viability of the cartilage in a cryopreserved tracheal allograft by measurement of Na235SO4 incorporation. We also investigated the effects of warm ischemic time on tracheal cartilage viability.

Methods. The tracheas from Lewis rats were harvested and preserved at different warm ischemic times from cardiac death to preservation (0, 1, 2, 4, 6, 9, and 12 hours, each group n = 8). The cartilage was labeled with 4 µCi/mL of Na235SO4. The specimen was hydrolyzed in 0.5 mol/L NaOH, and a solution of the extracts was then counted by liquid scintillation counter. Tracheas were transplanted into Brown Norway rats.

Results. 35Sulfur incorporation in the cartilage decreased as warm ischemic time increased. In addition, 35Sulfur incorporation decreased from 76% to 67% after cryopreservation. Histologic examinations of the normal tracheal cartilage before preservation and after thawing were done in all the groups. After transplantation, the cartilage had severe fibrous changes, and its layer was almost nonobservable in the 9- and 12-hour groups.

Conclusions. The viability of the tracheal cartilage decreased with warm ischemic time and from 76% to 67% after cryopreservation. In the rat tracheal transplantation model, a cryopreserved tracheal allotransplant could be done safely with a graft that was cryopreserved within 6 hours of warm ischemic time.




This article has been cited by other articles:


Home page
Ann. Thorac. Surg.Home page
K. Kushibe, K. Nezu, K. Nishizaki, M. Takahama, and S. Taniguchi
Tracheal allotransplantation maintaining cartilage viability with long-term cryopreserved allografts
Ann. Thorac. Surg., May 1, 2001; 71(5): 1666 - 1669.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ANN THORAC SURG ASIAN CARDIOVASC THORAC ANN EUR J CARDIOTHORAC SURG
J THORAC CARDIOVASC SURG ICVTS ALL CTSNet JOURNALS
Copyright © 2000 by The Society of Thoracic Surgeons.