Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9834
Title: Relationship between ATP resynthesis and calcium accumulation in the reperfused rat heart.
Austin Authors: Hasin, Y;Kneen, M M;Craik, D J;Nayler, W G
Affiliation: Department of Medicine, University of Melbourne, Austin Hospital, Heidelberg, Victoria, Australia
Issue Date: 1-Feb-1992
Publication information: Clinical and Experimental Pharmacology & Physiology; 19(2): 79-87
Abstract: 1. The postulate that the composition of solutions used to reperfuse ischaemic hearts may modulate their ability to synthesize high-energy compounds was tested in isolated rat hearts subjected to 30 min normothermic ischaemia and then reperfused with either Krebs'-Henseleit buffer (K-H) for 20 min (control reperfusion, CR), or a 'myocardial protective solution' (MPS) for 5 min, followed by 15 min K-H (modified reperfusion, MR). The 'myocardial protective solution' was designed to protect against damage caused by sodium and calcium accumulation and by free radicals. Metabolic precursors were also included to promote and support adenosine triphosphate (ATP) resynthesis during reperfusion under both aerobic and hypoxic conditions. 2. 31P nuclear magnetic resonance (NMR) was used to measure tissue ATP and creatine phosphate (CP), and atomic absorption spectrometry was used to measure Ca++. Early during CR, ATP recovered to 28% of the pre-ischaemic value, but fell to 5.5% with continued perfusion. Similarly, CP recovered to 45.5% of the pre-ischaemic level during early CR but fell to 25.5% with continued perfusion. 3. Better maintenance of ATP was seen during MR with oxygenated MPS (O2-MR), the final ATP remaining at 16.9% of the pre-ischaemic level. During O2-MR, CP recovered to 43.55 of the pre-ischaemic level but was not maintained and fell to a final level of 29.5%. 4. During MR with O2-free MPS (non-O2-MR), there was no reperfusion-associated fall in ATP or CP, with the levels maintained at 26.6% and 34.55, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
Gov't Doc #: 1555327
URI: https://ahro.austin.org.au/austinjspui/handle/1/9834
Journal: Clinical and Experimental Pharmacology & Physiology
URL: https://pubmed.ncbi.nlm.nih.gov/1555327
Type: Journal Article
Subjects: Adenosine Triphosphate.biosynthesis
Animals
Calcium.metabolism
Coronary Disease.metabolism
Female
Male
Myocardial Reperfusion
Myocardial Reperfusion Injury.prevention & control
Myocardium.metabolism
Phosphocreatine.metabolism
Rats
Rats, Inbred Strains
Appears in Collections:Journal articles

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