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VOLUME LOADI.'G EFfEC13ON THE HEARt USING "P NMR 147<br />

This inditates Nat 2 .3-DPG is present in too small a qudntity to cause a problem with<br />

contamination of in vira hean spectm. There were twro blood peaks (peak 1 . peak 2)<br />

in the s'P NMR spectra of cat blood . Peak one had a chemical shift consistent with<br />

dtat of P, . Peak two had a chemical shift consistent with that of a phosphodiester .<br />

Thus.any increase in the P, peak ofin viraspectm would most likeiy be that generated<br />

fmnt intracellular metabolism .<br />

Pln:ciologira/ lmrnrntirnr<br />

~ After control spectra were acquired . volume o.Yrload (high output state) was produced<br />

by opening the previously constructed abdominal aorta-vena cava shunts . a'P<br />

spectra were obtained sequentially at 6-min intervals o .er I to 2 h or acute volume<br />

loading. Upon opening of the AVS . all cats had the typical increase in pulse pressure<br />

which is a good indication that the shunt has been opened .<br />

N.71R Data Anahsis<br />

Each free induction decay (FlD) was Fourier tmnsformed and filtered with 10 Hz<br />

line bmadening Spectra .verc phased and curve fi0ed(Lorcnt8an) using a least-squarex<br />

fit algorithm. Areas under each peak were integrated . Each spcctrvm contained the<br />

following peaks from left to right : inorganic phosphate . phosphocrcatine. and adenosine<br />

triphosphate (ATP: T . a . tT). Figs. 3 and 4. Ratios of P,/PCr and PCr/ATP were used<br />

to estimate the slatc ofoaidati•r phosphopiation . The chemical shift of P, with respect<br />

to PCr was used to determine the pH of myocardial cells during physiological intervention<br />

.<br />

To determine the reproducibility of"P NhfR data, the following was done . Under<br />

• contrd conditions (no physiological intervention) . five sets of spectra were obtained<br />

at the beginning of each esperfinent and at the end of each experiment for each cat .<br />

P,IPCr and PCr/ATP data were averaged and the standard deviation was determined .<br />

TTere was ±6% variability for P,/PCr ratios from acquisition of one slxctnnn m the<br />

next and t 108% variability for PCr/ATP ratios. Thus, there is mme random variability<br />

in "P NMR data which must be acknowledged when responses to physiological in•<br />

tervention areevalualed . A change in the P~/PCr mtio of greater than 61, and a ch ange<br />

in the PCr/ATP ratio of greater than i0't, must ocrur for a responsc to be considered<br />

due to physiological intervention and not due to random variability .<br />

Bioenergetir data as determined by P,/PCr and PCr/ATP ratios were corrclated<br />

with mechanical function as determined by hean m1e x systolic blood pressureprodun<br />

lHR x SBP is an estimate of oxygcn consumption (27)) with a linear regression algorithm<br />

. In addition, in order to follow changes in the above-mentioned parameters<br />

• with time and intervention (i .e . . to observe the effects of continuous modulation of<br />

feedback control ofchanges in wark load on metabolism and vice versa). percentage<br />

changes of P,/PCr, PCr/ATP. and HR x SBP from control were plotted with respect<br />

• to time and intervention .<br />

•<br />

http://legacy.library.ucsf.edu/tid/fpe59c00/pdf<br />

RESULTS<br />

Although all animals were prepared and treated in a similar manner concerning<br />

maintenance of stable physiological conditions (maintenance of arterial blood gases .<br />

PUBLICATIONS 028396<br />

10347653

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