Proton magnetic relaxation in bone marrow related to age and bone mineral density: low-resolution in vitro studies.

Detailed analysis of proton spin-spin and spin-lattice relaxation behaviors of the bone marrow in the presence of trabecular bone network was performed at low-resolution (B(0) = 0.496T) on rat vertebrae specimens deprived of spinal cord. Two groups of samples, from young and old healthy animals, were investigated before cellular necrosis had started. BMD measurements were carried out to quantify the expected age-related modifications of the trabecular bone network. 1H-MR measurements were also performed on the same samples, deprived of marrow and saturated with water, in order to control the validity of a possible interpretation of the marrow 1H-MR characteristics, in terms of marrow components, and to investigate the possible employment of these samples to study the trabecular bone network properties. We pointed out that: 1) a bimodal distribution of T(2i) and T(1i) values (distinguishing "fast" and "slow" relaxations) describes satisfactorily all the 1H-MR experimental decays; 2) age-related modifications of the trabecular bone network are marked by correlate variations of the BMD value and of the proton spin-spin relaxation rates in water saturated samples; 3) age-related modifications of marrow are underlined by variations of the average value of the "fast" T(2i) and of the "slow" T(1i) relaxation time distributions, which could be attributed to the marrow components different from the fat granules of the adipose cells. Our results suggest that studies in vitro on bone tissue, by 1H-MR techniques at low-resolution, may contribute to a better bone function characterization and, therefore, to a better clinical utilization of MRI techniques.

Analysis of the first international data bank on in vitro NMR relaxation times: animal liver.

Based on an international "Interlaboratory Comparison of Protocol Trials for In Vitro Studies by NMR," the EEC COMAC-BME concerted action on "Identification and Characterization of Biological Tissue by NMR" started collection of a data bank for in vitro relaxation time data of normal and pathological tissues. Relaxation time measurements were performed in a frequency range from 10-90 MHz and in a temperature range from 3 to 40 degrees C; data analysis was done using single exponential fitting routines. Specimens were taken from different organs or tissues (n = 19) of various species (n = 5) and both sexes. More than 900 relaxation time data from 12 participating groups were collected. However, for quantitative analysis we concentrated on liver tissue (287 entries). Main results are the high reproducibility of data from different centers, allowing quantification of temperature dependence of T1 and T2, respectively, in fresh mouse (3.9 and 0.41 msec/degrees C), rat (2.1 and 0.24 msec/degrees C), and hamster (2.6 and 0.22 msec/degrees C) liver. Further, a highly significant species difference between mouse and rat liver, not depending on water content, has been established. We discuss results quantitatively as well as consequences for in vitro protocols and future multicenter data collection.

Variations of the 1H spin-lattice relaxation in a fatty liver model as compared to normal liver.

We report the results of an in vitro study on ethionine-injected rat liver (EI) and on normal rat liver (C) performed analyzing with iterative fitting procedures the 1H spin-lattice relaxation curves detected by IR pulse sequence at 20 MHz and at 37 degrees C on fresh excised samples. Single-exponential functions did not adequately describe the experimental curves both in EI and in C group. The analysis of the curves by two-exponential hypothesis showed a small portion of the signal characterizable by a time constant of about 80 ms, common both to EI and to C samples. A slowing of about 30% in the relaxation characterized the remaining portion of the curve (90-95%) in EI as compared to C samples. The hypothesis that the 1H of the triglycerides vacuoles present in EI livers had a relaxation curve additional to the remaining signal was checked by three-exponential analysis. The results were not in contrast with the known value of the triglycerides percentage content and with the spin-lattice relaxation time of the -CH2 group 1H obtained in different experimental conditions in the same fatty liver model. The negative results of the three-exponential analysis on normal liver curves as well as the favorable controls performed to test the analysis procedure supported further this hypothesis. The remaining signal after subtraction of the triglycerides contribution showed still the small fast portion and the increase of the relaxation time of the major portion (from approximately 300 ms up to approximately 400 ms) as compared to C samples.(ABSTRACT TRUNCATED AT 250 WORDS)

The water proton spin-lattice relaxation time measurements in liver samples from hepatectomized and sham-operated rats.

We report the proton spin-lattice relaxation times (T1) of rat liver samples taken at different times after partial hepatectomy. The T1 values obtained are compared with those of liver samples from sham-operated rats and of liver samples from rats that had not undergone any surgical treatment. The results show that surgical stress significantly influences the T1 values of sham-operated rats both in their absolute value and in their dependence on the time after the operation, while it induces only a modest early increase of the water content. Possible effects of liver regeneration on 1H-T1 are almost completely concealed by the changes due to the surgical operation. These results emphasize the importance of the choice of a suitable control for T1 measurements in biological systems.