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Biomedical subjects

I Imanaga

Publications and source records attributed to I Imanaga.

47 records · Page 3Linked to original sources
PubMed1987

Cell-to-cell diffusion of fluorescent dyes in paired ventricular cells.

The intracellular and cell-to-cell diffusion of fluorescent dyes of various molecular sizes were studied in enzymatically isolated paired ventricular cells of the guinea pig heart. Fluorescein sodium (mol wt 332), 6-carboxyfluorescein (mol wt 376), Lucifer yellow CH (mol wt 457), lissamine rhodamine B-200 (mol wt 559), and tetraglycine-conjugated lissamine rhodamine B-200 (mol wt 859) were all diffused into the single ventricular cell through the patch-clamp pipette. All these dyes were able to diffuse through the gap junction of the paired cells. The diffusion coefficient of 6-carboxyfluorescein in the cytoplasm was 5.8 X 10(-6) cm2/s, Lucifer yellow CH was 3.0 X 10(-6) cm2/s, and lissamine rhodamine B-200 was 8.6 X 10(-7) cm2/s. Permeability of the gap-junctional membrane was 6.8 X 10(-4) cm/s for 6-carboxyfluorescein, 2.8 X 10(-4) cm/s for Lucifer yellow CH and 7.4 X 10(-5) cm/s for lissamine rhodamine B-200. Thus lissamine rhodamine B-200 diffused in the cytoplasm and through the gap junction approximately 10 times slower than 6-carboxyfluorescein. Tetraglycine-conjugated lissamine rhodamine B-200 (mol wt 859) passed through the gap junction, suggesting that the critical pore size of the ventricular gap junction may be somewhat larger than that of the conjugated tetraglycine rhodamine.

Animals↗
PubMed1987

The long-lasting contraction induced by transmural stimulation in the longitudinal muscle of the guinea-pig gastric corpus.

The mechanisms involved in the long-lasting contraction induced by transmural stimulation were investigated in the isolated longitudinal muscle of the guinea-pig gastric corpus. Transmural stimulation induced an initial rapid contraction, a subsequent relaxation and a long-lasting contraction which was mimicked closely by the responses to noradrenaline and ATP. The rapid contraction was blocked by tetrodotoxin or by atropine, and the subsequent relaxation was also blocked by tetrodotoxin, but not by atropine. The long-lasting contractions were not inhibited by atropine, phentolamine, and propranolol. However, some of those were partially inhibited by tetrodotoxin and guanethidine, and others were enhanced by tetrodotoxin. The noradrenaline- but not ATP-induced long-lasting contraction was blocked by phentolamine. Furthermore, indomethacin completely abolished the long-lasting contractions induced by transmural stimulation, noradrenaline, and ATP, but did not significantly affect the response to prostaglandin E2. The results indicate that the long-lasting contraction induced by transmural stimulation is mediated through prostaglandins release which may be triggered by neuro-transmitters or by endogenous substances.

Adenosine Triphosphate↗
PubMed1979

[Comparison of the effects of dobutamine with dopamine and isoproterenol on inotropism and chronotropism in the mammalian heart (author's transl)].

The effects of dobutamine on inotropism and chronotropism of the heart were studied in vivo and in vitro and were compared with those of dopamine and isoproterenol. These compounds increased epicardial contractile force and the heart rate of the open-chest, bilaterally vagotomized dog under pentobarbital anesthesia. The dose-ratio for the contraction was [dobutamine: dopamine: isoproterenol = 1:0.8:40] and for the heart rate, [= 1:1:300]. Both drugs augmented the twitch contraction of the isolated dog ventricular papillary muscle with the dose-ratio of [dobutamine: dopamine: isoproterenol = 1:0.7:11]. This mechanical response was associated with an elevation of the plateu voltage and an increase in repolarization of the action potential, but with no alteration of the maximum rate of rise of the action potential, the resting potential and the input membrane resistance. The discharge frequency of the rabbit S-A node pacemaker potential was accelerated chiefly due to an increase in the slope of the diastolic slow depolarization. With concentration of these catecholamines for the equivalent positive inotropic potency on the papillary muscle, this effect of isoproterenol was more potent than the effects of dobutamine and dopamine. These positive inotropic and chronotropic actions of the catecholamines were abolished by a beta-receptor antagonist. Those actions of dopamine were markedly reduced by reserpine pretreatment. In addition, dobutamine had little vascular effect. These results indicatte that dobutamine has a positive inotropic effect and a less positive chronotropic effect and that such is due to the direct action on the ventricular myocardium and the S-A node through beta 1-adrenergic receptors.

Action Potentials↗
PubMed1977

A comparative study of the effects of OPC-1085 and propranolol on isolated guinea pig atrium.

Effects of a newly synthesized beta-blocker, 5-(3-tert-butylamino-2-hydroxy) propoxy-3,4-dihydrocarbostyril (OPC-1085) were compared with those of propranolol. OPC-1085 had a potency about 3 times greater than that of propranolol in blocking the positive inotropic and chronotropic effects of isoprenaline on the isolated guinea pig atrium. At a concentration of over 3 X 10(-5) M OPC-1085 produced negative inotropic and chronotropic effects. However, these effects were about 10 times weaker than those of propranolol. Suppressing effects on the rate of rise and on the maximum driving frequency of action potentials were also more than 10 times less than those of propranolol. There was almost no change in the action potential of vagus nerve after a 10 min treatment with OPC-1085 (10(-5) M), while the action potential was reduced to 60-70% with propranolol (10(-5) M).

Action Potentials↗
PubMed1975

Low resistance pathways between myocardial cells.

To test the hypothesis of whether the intercalated discs represent a low resistance to diffusing ions, a method was developed to study the longitudinal diffusion of radioactive potassium (42K), tetraethylammonium ([14C]TEA), and the fluorescent dye Procion yellow (PY) in sheep and calf heart bundles. The method involved 1) loading the cells, 2) allowing the ions to diffuse for periods of 2-6 hr, 3) freezing the bundle in liquid air and cutting it into equal slices of 0.5 mm, 4) measuring the concentration of the ion in each slice. From the results, the diffusion of coefficients were considered to be due partially to the discs and partially to the myoplasm. The permeabilities of the nexal membranes were 7.68-10(-3), 1.27-10(-3), and 1.4-10(-6) cm/sec for 42K, 14C-TEA, and PY. These values are 9,600, 21,000, and 220 times more than the corresponding ones for the surface membrane. The disc resistance for potassium, the main intracellular charge carrier, was about 0.9 ohm cm2. From the van der Waals sizes of the ions, the diameter of the nexal pores has to be 10-15 A. It is concluded that the junctions between myocardial cells have low resistances and that propagation of action potentials is possible by local circuit currents.

Animals↗
PubMedDate not supplied

Effects of insulin on mammalian cardiac muscle.

Insulin increases the contractile force of myocardium with hyperpolarization and a faster rate of fall of the action-potential plateau. This phenomenon is augmented inthe reduced-K+ or ouabain solution. It is suggested that the insulin-induced positive inotropism can be explained by facilitation of inward movement of Ca2+, which possibly is associated with an increase in outward movement of K+.

Action Potentials↗