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Biomedical subjects

S Ichikawa

Publications and source records attributed to S Ichikawa.

At least 289 records · Page 16Linked to original sources

Nonuniform action potential durations at different sites in canine left ventricle.

We studied the action potential duration (APD) of isolated ventricular muscle fibers. Action potentials were recorded from four different sites (endocardium and epicardium at the apex and the base) in the canine left ventricle by microelectrode techniques. Action potentials from endocardial and corresponding epicardial specimens, and the differential potential between them were recorded simultaneously. The APDs at 60% and 90% repolarization (APD60 and APD90) were measured during superfusion with normal (K+ = 2.7 mM) and altered (K+ = 5.4 mM) Tyrode's solutions. Results were: 1) the distributions of APDs agreed with previous descriptions from in vivo studies; 2) endo-epicardial APD gradients were different between the apex and the base, and apico-basal APD gradients were different between endocardium and epicardium; 3) the shapes of the differential potentials in normal and altered Tyrode's solution were similar to the electrocardiographic T wave form in normal and in mild hyperkalemia. It was concluded that nonhomogeneous APDs may be due to the inherent characteristics of cardiac muscle and the nonuniform endo-epicardial APD gradient helps to account for the genesis of the electrocardiographic T wave form.

Action Potentials↗

Animal model of megaureter.

A rabbit model with a megaureter was produced by the partial obstruction of the ureter. The resultant dilatation obtained after the chronic obstruction (more than 100 days) was approximately 4 times greater than the normal ureteral diameter.

Animals↗

ATPase activity and calcium uptake of microsomes isolated from stomach smooth muscle after exposure to phospholipase C.

ATPase activity and Ca2+ uptake were examined in microsomal membrane fractions isolated from guinea pig stomach smooth muscle which had been exposed to phospholipase C (PLC). Basal Mg2+-ATPase, Na+, K+-ATPase and Ca2+, Mg2+-ATP activities were inhibited in a time dependent manner by PLC treatment. There was positive correlations between each of these ATPase activities and total phospholipid content of the microsomal fraction. Phosphotidylcholine restored Ca2+, Mg2+-ATPase activity of the microsomal fraction isolated from the tissue which had been treated with PLC for 30 min but not after 60 min. Ca2+ uptake in the presence of ATP by microsomal fraction from tissue treated with PLC for 60 min was significantly decreased. The results provide a cellular basis for the inhibitory effect of PLC on contractility of stomach smooth muscle.

Adenosine Triphosphatases↗

Effect of corpora lutea on placental hypertrophy in rats.

Prepubertal rats, induced to mate by treatment with pregnant mare serum gonadotrophin (sperm present = day O), were used in all experiments. The reduction in the number of corpora lutea (CL) of pregnancy to four on days 10 or 13 of pregnancy produced placental hypertrophy when compared to sham-operated controls, but a reduction to six had no effect on placental growth. The removal of all primary CL on days 11 or 13 of pregnancy in pregnant rats bearing additional secondary CL induced by an injection of human chorionic gonadotrophin (hCG) on days 5 or 7 of pregnancy also resulted in placental hypertrophy. Ovarian secretion of progesterone on day 13 of pregnancy was significantly lowered after reducing CL to four in normal pregnant rats and removing primary CL from rats treated with hCG on day 5. Removal of primary CL from rats treated with hCG on day 5 had no effect on oestradiol-17 beta secretion, whereas reducing CL to four in normal pregnant rats significantly increased it. Daily injections of 4 mg progesterone until day 17 of pregnancy from the day of reduction of the number of CL, or from the day of removal of primary CL, prevented placental hypertrophy. These results suggest that the decrease of progesterone, but not of oestrogen, is the main factor inducing placental hypertrophy in ovariectomized pregnant rats.

Animals↗

Pressor responses to vasopressin in rabbits with 3-day renal artery stenosis.

One-kidney rabbits were subjected to renal artery stenosis, and acute experiments were performed 3 days later on conscious animals; one-kidney rabbits without renal artery stenosis served as controls. Rabbits with 3-day renal artery stenosis were normotensive and had normal values for plasma renin activity. Intravenous infusion of arginine vasopressin at 5 mU.min-1.kg body wt-1 for 5 min resulted in a significantly (P less than 0.01) greater increase in mean arterial pressure and total peripheral resistance (TPR) in the renal artery stenosis rabbits than in the controls. Infusion of the angiotensin II (AII) competitive antagonist, [Sar1, Ile8]AII, before the vasopressin infusion abolished the hyperresponsiveness to vasopressin in the renal artery stenosis rabbits and resulted in changes in mean arterial pressure and TPR that were approximately of the same magnitude as the controls. Infusion of [SAr1, Ile8]AII before vasopressin infusion in control rabbits did not alter the cardiovascular responses to vasopressin. Because previous studies have shown that 3-day renal artery stenosis rabbits have exaggerated pressor responses to norepinephrine and that this hyperresponsiveness to norepinephrine is blocked by [Sar1, Ile8]-AII, the present study with vasopressin provided evidence that the increased responsiveness in this model is not specific for a single pressor agent. These studies also demonstrated that AII plays an important role in mediating the exaggerated pressor responses to vasopressin in this prehypertensive model.

Animals↗

Effect of dexamethasone on the diurnal rhythm of plasma aldosterone in patients with congestive heart failure.

Diurnal rhythm studies were performed on 11 patients with congestive heart failure. Blood samples were taken for the determination of aldosterone, cortisol and plasma renin activity every 4 hours from 12:00 a.m. to 12:00 a.m. the following day. Following this control study, a second diurnal rhythm study was conducted under dexamethasone treatment (0.5 mg of dexamethasone every 4 hours for 48 hours). In the control study, aldosterone and cortisol fluctuated showing a diurnal rhythm with the lowest value in the evening and the highest value in the morning. Plasma renin activity rhythm was indistinct. Fluctuations in plasma renin activity were not parallel with aldosterone. Dexamethasone treatment suppressed cortisol to less than 1 microgram/100 ml. Aldosterone values decreased significantly in the morning (p less than 0.01); this was accompanied by the abolishment of aldosterone rhythm. Plasma renin activity rhythm remained indistinct following administration of dexamethasone. These results suggest that adrenocorticotrophic hormone plays an important role in the control of aldosterone diurnal rhythm in patients with congestive heart failure.

Adolescent↗

In situ monitoring with Tradescantia around nuclear power plants.

Highly sensitive mutational responses of the stamen-hair system of some Tradescantia clones heterozygous for flower color (blue/pink, the blue being dominant) to low-level radiation and chemical mutagens, as demonstrated in the last decade, seem to endorse this system to be the most promising biological tester for detecting the genetic effects of mutagens at low levels. Two triploid (thus sterile) clones, KU 7 and KU 9, have been established as those suitable for in situ monitoring of environmental mutagens. In situ monitoring with such Tradescantia clones was first tried in 1974 around a nuclear power plant in Japan, then has been repeated until 1979 around more nuclear plants. About 260,000 to 1,570,000 stamen hairs were observed per year per nuclear plant (about 12-million hairs in total), and the data of pink mutation frequency were analyzed statistically. Significantly increased mutation frequencies were observed and were correlated to the operation periods of the nuclear facilities and to predominant wind direction, but not to other environmental factors. Considering physical monitoring data of radiation dose in the air, internal exposure due to incorporation and concentration of man-made radioactive nuclides seems to be of a greater importance in increasing mutation incidence.

Air Pollutants↗

[Effects of adrenaline, noradrenaline and pilocarpine on the oxygen uptake in rat submandibular gland (author's transl)].

This investigation was undertaken to clarify the oxygen uptake caused by adrenaline, noradrenaline and pilocarpine in rat submandibular gland. 1. Adrenaline (55 microM), noradrenaline (55 microM) and pilocarpine (10 microM) significantly stimulated the oxygen uptake. 2. When Na+ in Ringer solution was substituted by Li+ or choline, the stimulation by adrenaline, noradrenaline and pilocarpine was blocked. However, when Na+ (50%) was contained in the Li+ -Ringer solution, the response by these agents were observed. 3. When K+ in the Ringer solution was removed, the stimulation by adrenaline and noradrenaline was observed, but that by pilocarpine was not. 4. Adrenaline-, noradrenaline- and pilocarpine-induced oxygen uptake was not observed when Ca2+-deficient tissue was incubated in Ca2+-free Ringer solution. When the normal tissue was incubated in Ca2+-free Ringer solution, the stimulation by adrenaline and noradrenaline was observed, but that by pilocarpine was diminished. 5. The oxygen uptake of Ca2+-deficient tissue due to adrenaline and noradrenaline was recovered by the addition of 3 or 5 mM Ca2+ to the Ca2+-free Ringer solution, while the response of pilocarpine was recovered by the addition of 5 mM Ca2+. 6. The stimulation by adrenaline, noradrenaline and pilocarpine was considerably blocked by the addition of 2.5 or 5 mM La3+ to the Ringer solution. 7. The stimulation by adrenaline and noradrenaline was significantly blocked by the addition of 5 mM procaine. On the other hand, the stimulation by pilocarpine was blocked by 0.5 or 5 mM procaine. These results suggest that the increase in the oxygen uptake seen with adrenaline, noradrenaline and pilocarpine is dependent on the presence of Na+ and Ca2+.

Animals↗