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J Watanabe

Publications and source records attributed to J Watanabe.

At least 559 records · Page 31Linked to original sources

Binding and internalization of 125I-glucagon in hepatocytes of intact mouse liver. An autoradiographic study.

Localization of labeled material in hepatocytes of intact mouse liver injected via the portal vein with 125I-glucagon was studied. At 3 minutes after pulse injection of the labeled glucagon, most grains were localized associated with the plasma membrane. At 10 min after the injection, the grains were distributed throughout the cytoplasm and did not appear localized exclusively in any specific cell organelles. At 20 min after the injection, the labeled material appeared decreased, and was not yet localized exclusively in any specific cell organelles. Thus, in hepatocytes of intact liver, labeled glucagon is internalized more rapidly than in freshly isolated hepatocytes (Barazzone et al. 1980), and there appear to be no cell organelles in which internalized glucagon is preferentially localized.

Animals↗

Effects of afterload reduction on global left ventricular and regional myocardial functions in the isolated canine heart with stenosis of a coronary arterial branch.

We examined the effects of graded reduction of afterload on the global left ventricular and regional myocardial functions as well as coronary hemodynamics in hearts with regional ischemia. We used isolated, paced canine hearts that were loaded with a hydraulic system that simulated the aortic input impedance of the dog's arterial tree. The loading conditions could be quantitatively and sequentially changed by the reduction of the systemic vascular resistance of the hydraulic system, while the preload was kept constant using a variable-height reservoir connected to the left atrium. The heart was perfused with arterial blood from a support dog. Mean coronary perfusion pressure was maintained equal to mean aortic pressure (AoP) by a servo-controlled pump. Then, the left circumflex branch was constricted to an approximate 50% flow reduction of the preischemic control condition. The myocardial lengths at ischemic and nonischemic regions were measured with two pairs of ultrasonic crystals. In the hearts without ischemia, cardiac output continued to increase, from 535 +/- 14 to 1181 +/- 74 ml/min (p less than 0.01), as mean AoP decreased fom 111 +/- 4 to 52 +/- 3 mm Hg (p less than 0.01), although mean coronary blood flow decreased by approximately 50%. During regional ischemia, at control pressures, performance of the ischemic region diminished from 0.94 +/- 0.15 to 0.77 +/- 0.15 mm (p less than 0.05). With a small decrease in afterload, from 98 +/- 6 to 86 +/- 3 mm Hg, performance improved slightly as in the normal region. With a larger reduction in afterload, from 86 +/- 3 to 55 +/- 6 mm Hg, performance of the ischemic region decreased from 0.77 +/- 0.15 to 0.61 +/- 0.15 mm (p less than 0.05) while cardiac output increased. Thus, there appears to be a bimodal change in performance: a baseline performance, perfusion pressure-mediated decrease and a second, afterload-modulated change.

Animals↗

The change of disposition kinetics for creatinine and urea accompanied by growth in mice.

In order to clarify the change of disposition kinetics accompanied by growth, the whole-blood levels and whole-body autoradiography following intravenous administration of creatinine and urea, which are considered to pass through the water-filled pores of biological membranes easily, were investigated in 1-day-old, 1-week-old, 3-week-old and 8-week-old mice. For both creatinine and urea, the total body clearance was considerably lower in 1-day-old and 1-week-old mice than in more aged mice. Relatively lower renal clearance (i.e. rather incomplete renal function) in 1-day-old and 1-week-old mice was considered to be the major reason for this observation. Moreover, the lower metabolic clearance also seemed to be the cause in the case of urea, because the expiratory excretion of 14CO2 following the intravenous administration of 14C-urea was almost negligible in 1-day-old and 1-week-old mice in contrast to more aged (16-21%). The whole-body autoradiograms obtained following intravenous administration of 14C-creatinine indicated that creatinine was more rapidly transferred from blood to muscle in 1-day-old and 1-week-old mice, especially in 1-day-old mice, than in more aged mice. This might be caused by the difference in muscular blood flow rate or muscular cell membrane permeability to creatinine.

Aging↗

The change of disposition kinetics for thiourea accompanied by growth in mice.

The whole blood levels and whole-body autoradiography following intravenous administration of thiourea, which is considered to covalently bind to the macromolecules in the body, were investigated in 1-day-old, 1-week-old, 3-week-old and 8-week-old mice in order to clarify the change of disposition kinetics accompanied by growth. The total body clearance for thiourea was remarkably lower in 1-day-old and 1-week-old mice than in more aged mice. The lower metabolic clearance as well as renal clearance in 1-day-old and 1-week-old mice seemed to be responsible for this observation. The whole-body autoradiograms obtained at 60 min following intravenous administration of 14C-thiourea showed the homogeneous distribution of radioactivity throughout the body in 1-day-old and 1-week-old mice and the high radioactivity localized in the liver and lung in more aged mice. This remarkable difference was assumed to be brought about by the difference in quantity of the macromolecules in the liver and lung which can covalently bind with thiourea. This assumption was supported by the result of gel filtration on Sephadex G-10 of the liver and lung homogenates.

Aging↗

Disposition of fractionated 3H-heparin in rats.

To evaluate the disposition of fractionated 3H-heparin, high affinity fraction (fraction A) and low affinity fraction (fraction NA) to protamine were prepared in this study from commercial 3H-heparin by affinity chromatography on protamine-Sepharose and gel filtration chromatography. Following intravenous administration of fraction A to rats, it seemed that the radioactivity in plasma declined one-exponentially with time to a pseudo-steady-state level, and 20.5% of dose was excreted in urine in 5 h. However, following the administration of fraction NA to rats, the plasma radioactivity curve was different from that of fraction A, and 69.8% of dose was excreted in urine in 5 h. It was found that fraction A and fraction NA had the distinctly different disposition characteristics in the body. Additionally, whole-body autoradiography with fraction A showed that the liver, bone marrow, kidney cortex, salivary gland and intestine played an important role in the distribution of it. It was suggested by gel filtration chromatography and affinity chromatography that the main material of the radioactivity excreted in urine in 5 h has the same properties as that of the administered heparin fraction.

Animals↗

[A case of anorectal malignant melanoma with liver metastasis reduced subjective symptoms by transcatheter arterial embolization].

We report a 56-year-old female with anorectal malignant melanoma reduced subjective symptoms by transcatheter arterial embolization (TAE). She had five-month history of melena and epigastric fullness. The physical examination revealed anorectal tumor and hepatomegaly. Pathological examination of the tumor and liver CT scan showed anoreectal malignant melanoma with liver metastasis. Surgical excision of the anorectal lesion and TAE against the liver metastasis improved subjective symptoms remarkably. Liver CT scan after TAE showed necrosis of the metastatic tumors. TAE is effective for palliative treatment of liver metastasis of anorectal malignant melanoma.

Anus Neoplasms↗