Abstract | BACKGROUND: METHODS: C57BL/6CrSlc(B6) mice underwent syngeneic mice heterotopic heart transplantation, and the animals were derived into 3 groups: recipients with nonpreserved grafts (control group), recipients with grafts preserved in histidine- tryptophan-ketoglutarate (HTK) for 24 and 48 hours (HTK group), and recipients with grafts preserved in SS-II for 24 and 48 hours (SS-II group). RESULTS: After 48 hours of preservation, there were no grafts that survived in the HTK group; however, the SS-II group had a high survival rate. After 24 hours of preservation, SS-II decreased the oxidative damage, myocardial apoptosis, and the infiltration of macrophages and neutrophils in the cardiac grafts in the early phase and suppressed the development of myocardial fibrosis in long-term grafts compared with HTK. CONCLUSIONS: The SS-II prolongs the acceptable cold storage time and protects the myocardium from I/R injury via inhibiting oxidative stress-associated damage. We believe that this novel preservation solution may be simple and safe for use in the clinical transplantation field.
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Authors | Songjie Cai, Naotsugu Ichimaru, Mingyi Zhao, Masayuki Fujino, Hidenori Ito, Urara Ota, Motowo Nakajima, Tohru Tanaka, Norio Nonomura, Xiao-Kang Li, Shiro Takahara |
Journal | Transplantation
(Transplantation)
Vol. 100
Issue 5
Pg. 1032-40
(05 2016)
ISSN: 1534-6080 [Electronic] United States |
PMID | 26845308
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antioxidants
- Membrane Proteins
- Organ Preservation Solutions
- Organophosphorus Compounds
- Reactive Oxygen Species
- ascorbate-2-polyphosphate
- Heme Oxygenase-1
- Hmox1 protein, mouse
- Magnesium
- Cysteine
- Ascorbic Acid
- Glycine
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Topics |
- Animals
- Antioxidants
(chemistry)
- Apoptosis
- Ascorbic Acid
(analogs & derivatives, chemistry)
- Cold Temperature
- Cryopreservation
- Cysteine
(chemistry)
- Glycine
(chemistry)
- Graft Survival
- Heart
(drug effects)
- Heart Injuries
(pathology)
- Heart Transplantation
(methods)
- Heme Oxygenase-1
(metabolism)
- Macrophages
(metabolism)
- Magnesium
(chemistry)
- Male
- Membrane Proteins
(metabolism)
- Mice
- Mice, Inbred C57BL
- Mitochondria
(metabolism)
- Myocardium
(metabolism)
- Neutrophils
(metabolism)
- Organ Preservation
- Organ Preservation Solutions
(chemistry)
- Organophosphorus Compounds
(chemistry)
- Oxidative Stress
- Reactive Oxygen Species
(metabolism)
- Reperfusion Injury
(therapy)
- Time Factors
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