Article: Recipient FK506 pretreatment regimens in rat small bowel transplantation: allograft survival, function, and systemic infection
| Title | Recipient FK506 pretreatment regimens in rat small bowel transplantation: allograft survival, function, and systemic infection |
|---|---|
| Authors | Guo, WH1 2 3 Tian, L1 2 3 Yuen, ZW1 2 3 Chan, KL1 2 3 Wo, JYH1 2 3 Nicholls, G1 2 3 Dallman, M1 2 3 Tam, PKH1 2 3 |
| Issue Date | 2000 |
| Publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/jpedsurg |
| Citation | Journal of Pediatric Surgery, 2000, v. 35, p. 1600-1605 [How to Cite?] DOI: http://dx.doi.org/10.1053/jpsu.2000.18326 |
| Abstract | Purpose: Successful Small Bowel Transplantation Requires Effective Immunosuppression That Preserves Intestinal Function But Avoids Opportunistic Infection. This Study Aims To Evaluate Fk506 As A Single Immunosuppressant In Different Pretreatment Regimens In A Rat High Responder Strain Combination. Methods: Lewis → Da Rat Heterotopic Small Bowel Transplantation Was Performed. Studied Groups Were (1) Untreated Control, N = 12; (2) Fk-1, N = 8; (3) Fk-3, N = 8. Fk506 (2 Mg/Kg/D, Intramuscularly) Was Given To The Recipients For 1 Day (Fk-1) And 3 Days (Fk-3) Before Small Bowel Transplantation, Followed By 2 Weeks Of Subtherapeutic Treatment (0.3 Mg/Kg/D, Intramuscularly) After Small Bowel Transplantation. Syngeneic Small Bowel Transplantation Also Was Performed (N = 8). Fk Blood Levels, Maltose Absorption Test, Histology, And Bacteriology Were Performed At Different Postoperative Days. Results: Allograft Survival Was Prolonged Significantly With Fk Pretreatment, Being More So In Fk-3 Group (Fk-1, 22.2 ± 1.5 D; Fk-3, 40.7 ± 14.1 D; Control, 6.6 ± 0.8 D; P < .01). In The First Postoperative Week, Fk Blood Level Was Significantly Higher In Fk-3 Group (19.8 ± 1.5 Ng/Ml) Than In Fk-1 Group (5.0 ± 0.4 Ng/Ml; P < .05). There Was No Evidence Of Systemic Infection In Either Fk-Treated Group. For Maltose Absorption, Control Allograft Was Abnormal On Day 7 Correlating To Severely Damaged Intestinal Architecture. In Contrast, Fk-Treated Allografts Showed Well-Protected Intestinal Structure And Normal Absorption On Days 7 And 21. Conclusion: High Fk506 Blood Levels In The First Postoperative Week, Achieved With Fk Pretreatment, Prolonged Intestinal Allograft Survival And Preserved Intestinal Structure And Function Without Allowing Systemic Infection. Copyright (C) 2000 By W.B. Saunders Company. |
| ISSN | 0022-3468 2011 Impact Factor: 1.45 2011 SCImago Journal Rankings: 0.114 |
| DOI | http://dx.doi.org/10.1053/jpsu.2000.18326 |
| References | References in Scopus |
| dc.contributor.author | Guo, WH |
|---|---|
| dc.contributor.author | Tian, L |
| dc.contributor.author | Yuen, ZW |
| dc.contributor.author | Chan, KL |
| dc.contributor.author | Wo, JYH |
| dc.contributor.author | Nicholls, G |
| dc.contributor.author | Dallman, M |
| dc.contributor.author | Tam, PKH |
| dc.date.accessioned | 2010-09-06T08:40:00Z |
| dc.date.available | 2010-09-06T08:40:00Z |
| dc.date.issued | 2000 |
| dc.description.abstract | Purpose: Successful Small Bowel Transplantation Requires Effective Immunosuppression That Preserves Intestinal Function But Avoids Opportunistic Infection. This Study Aims To Evaluate Fk506 As A Single Immunosuppressant In Different Pretreatment Regimens In A Rat High Responder Strain Combination. Methods: Lewis → Da Rat Heterotopic Small Bowel Transplantation Was Performed. Studied Groups Were (1) Untreated Control, N = 12; (2) Fk-1, N = 8; (3) Fk-3, N = 8. Fk506 (2 Mg/Kg/D, Intramuscularly) Was Given To The Recipients For 1 Day (Fk-1) And 3 Days (Fk-3) Before Small Bowel Transplantation, Followed By 2 Weeks Of Subtherapeutic Treatment (0.3 Mg/Kg/D, Intramuscularly) After Small Bowel Transplantation. Syngeneic Small Bowel Transplantation Also Was Performed (N = 8). Fk Blood Levels, Maltose Absorption Test, Histology, And Bacteriology Were Performed At Different Postoperative Days. Results: Allograft Survival Was Prolonged Significantly With Fk Pretreatment, Being More So In Fk-3 Group (Fk-1, 22.2 ± 1.5 D; Fk-3, 40.7 ± 14.1 D; Control, 6.6 ± 0.8 D; P < .01). In The First Postoperative Week, Fk Blood Level Was Significantly Higher In Fk-3 Group (19.8 ± 1.5 Ng/Ml) Than In Fk-1 Group (5.0 ± 0.4 Ng/Ml; P < .05). There Was No Evidence Of Systemic Infection In Either Fk-Treated Group. For Maltose Absorption, Control Allograft Was Abnormal On Day 7 Correlating To Severely Damaged Intestinal Architecture. In Contrast, Fk-Treated Allografts Showed Well-Protected Intestinal Structure And Normal Absorption On Days 7 And 21. Conclusion: High Fk506 Blood Levels In The First Postoperative Week, Achieved With Fk Pretreatment, Prolonged Intestinal Allograft Survival And Preserved Intestinal Structure And Function Without Allowing Systemic Infection. Copyright (C) 2000 By W.B. Saunders Company. |
| dc.description.nature | link_to_subscribed_fulltext |
| dc.identifier.citation | Journal of Pediatric Surgery, 2000, v. 35, p. 1600-1605 [How to Cite?] DOI: http://dx.doi.org/10.1053/jpsu.2000.18326 |
| dc.identifier.doi | http://dx.doi.org/10.1053/jpsu.2000.18326 |
| dc.identifier.epage | 1605 |
| dc.identifier.hkuros | 62044 |
| dc.identifier.isi | WOS:000165100100017 |
| dc.identifier.issn | 0022-3468 2011 Impact Factor: 1.45 2011 SCImago Journal Rankings: 0.114 |
| dc.identifier.issue | 11 |
| dc.identifier.openurl | ![]() |
| dc.identifier.pmid | 11083432 |
| dc.identifier.scopus | eid_2-s2.0-0033759052 |
| dc.identifier.spage | 1600 |
| dc.identifier.uri | http://hdl.handle.net/10722/83352 |
| dc.identifier.volume | 35 |
| dc.language | eng |
| dc.publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/jpedsurg |
| dc.relation.ispartof | Journal of Pediatric Surgery |
| dc.relation.references | References in Scopus |
| dc.title | Recipient FK506 pretreatment regimens in rat small bowel transplantation: allograft survival, function, and systemic infection |
| dc.type | Article |
Author Affiliations
- Bristol Royal Hospital for Children
- The University of Hong Kong
- Imperial College London


