In memory of Syoten Oka--biorheologist and person (1907-1990). Oka's theories bearing on the vessel-blood organ and its EEFL interface.
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Biomedical subjects
Publications and source records attributed to A L Copley.
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Perihemorheology concerns the rheology of fluids and structures in the perivascular spaces. Furthermore, the term refers to the exchanges of rheological processes between the vessel-blood organ and its surrounding tissues, as well as in reverse. In 1960, the vessel wall and the circulating blood were considered by the author as an entity which in 1981 he postulated as an organ, named the 'vessel-blood organ', penetrating all other organs. This communication is not a survey but is intended to stimulate biomedical thinking regarding the importance of perihemorheology. The significance of the endoendothelial fibrin(ogenin) lining (EEFL) and fibrin(ogenin) as constituent of the interendothelial cement and the basement membrane in relation to perihemorheology is stressed. The role of albumin in the exchanges between hemorheology and perihemorheology is discussed. The protein content, as found by Witte, in the perivascular spaces as compared to the blood is emphasized regarding the importance of interrelations between the vessel-blood organ and rheological processes in the perivascular spaces. Recent studies, particularly by Laurent and his group, pertaining to hyaluronan in perivascular spaces and the blood demonstrate also the importance of the interrelationship between hemorheology and perihemorheology. The term 'blood-brain barrier', considered no longer to be adequate, is replaced by the term 'basement membrane-brain barrier'. It is proposed that the basement membrane of the vessel-blood organ penetrating the brain may contain certain constituents, unknown thus far, and may have a different structure from the basement membrane of the vessel-blood organ penetrating organs other than the brain.
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The steady state non-Newtonian viscosity of whole human blood has been widely studied as a function of the shear rate; and used to characterize the blood in various pathological disorders. In our previous studies, we demonstrated that blood is a thixotropic fluid. Its time-dependency and shear rate dependency of rheological behavior can be represented by an equation developed by Huang. Parameters of the equation can be used for the characterization of an individual's blood. They provide information, such as the kinetic rate constant of breakdown of RBC rouleaux to individual erythrocytes and the relative amount of rouleau formation in the dynamic equilibrium between rouleaux and individual erythrocytes. In this communication, the thixotropic parameters from blood samples of fifteen apparently healthy human subjects were investigated. When compared to the use of apparent viscosity values for the correlation with a pathological disorder, thixotropic parameters are preferable. The mean values of thixotropic parameters obtained from apparently healthy human subjects provide a base for comparison with the same parameters as obtained from blood samples of patients with certain pathological disorders involving the circulation.
The rheological properties of whole human blood exhibit thixotropic behavior at low shear rates up to about ten reciprocal seconds (1). The accepted cause of this shear rate-dependent and time-dependent behavior is the progressive breakdown of rouleaux into individual red cells. Huang developed a rheological equation which incorporates the kinetics of rouleau breakdown in his models (2). This five-parameter equation was used successfully to represent the hysteresis loop and the torque-decay curve of whole human blood. Numerical values of these five thixotropic parameters, which characterize the rheological behavior of the blood from apparently healthy human subjects, were established (3). In this communication, we examined the effect of hematocrit on each of the above mentioned parameters. The results show that the following parameters will increase their values with an increase in hematocrit: the yield stress, Newtonian contribution of viscosity, non-Newtonian contribution of viscosity, apparent viscosity and the equilibrium value of the structural parameter which indicates the relative amount of rouleaux in blood. Mathematical equations were developed to give the relationship between parameters and hematocrit. Two other thixotropic parameters, viz. the kinetic rate constant of rouleaux breakdown into individual red cells and the order of the breakdown reaction, were found to be independent of the hematocrit. It is consistent with reaction kinetic theory that the rate constant and the order of reaction are independent of the concentration of reactants.
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