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Biomedical subjects

K Haraguchi

Publications and source records attributed to K Haraguchi.

At least 163 records · Page 9Linked to original sources
PubMed1986

Iodide-induced hypothyroidism in a patient with anorexia nervosa.

A 39-year-old woman who had been suffering from anorexia nervosa was found to have hypothyroidism. Serum T4, free T4, T3, free T3 and TSH were 3.19 micrograms/dl, 0.5 ng/dl, 15.3 ng/dl, 1.2 pg/ml and 162.1 microU/ml, respectively. On careful questioning, she was found to have taken an iodine-rich diet. The serum iodine concentration was 122 micrograms/dl (normal: 4-9 micrograms/dl) and urinary iodide excretion was 13.05 mg/day (normal: less than 2 mg). After withdrawal of the iodine-rich diet, her serum T4 gradually increased and TSH returned to the normal range. She was diagnosed as having iodide-induced hypothyroidism. However, no significant elevation of serum T3 or free T3 was observed. Serum T4, free T4, T3, free T3 and TSH were 7.85 micrograms/dl, 0.8 ng/dl, 13.6 ng/dl, 4.3 pg/ml and 6.02 microU/ml, respectively. The iodide-perchlorate discharge test result was negative. These findings suggest that there exists some unknown mechanism by which a patient with anorexia nervosa may be sensitive to excess iodide. Furthermore, it is of interest to note that in a recovery phase from the hypothyroid state, normalization of serum T4 rather than T3 is well-correlated to TSH secretion.

Adult↗
PubMed1986

Effects of phorbol esters on protein phosphorylation and free T3 release by mouse thyroid lobes.

Phorbols stimulated 32P incorporation into several proteins in mouse thyroid lobes. Phosphoproteins (34 K and 23 K) were detected by SDS-polyacrylamide gel electrophoresis and autoradiography. Among phorbols tested, 12-O-tetradecanoyl-phorbol-13-acetate (TPA) was the strongest stimulator of protein phosphorylation. On the other hand, TPA at 50-200 ng/ml significantly stimulated free T3 release by mouse thyroid lobes. The stimulatory effect of TPA was not additive to that of TPA or dibutyryl cAMP. TSH stimulation of free T3 release by mouse thyroid lobes, however, was significantly inhibited by H-7 (an inhibitor of protein kinase C) at a concentration of 50 microM. These results suggest that protein kinase C may play some role in thyroid hormone secretion by phosphorylating the endogenous substrates.

1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine↗
PubMed1985

PCB and PCDF congeners in the blood and tissues of yusho and yu-cheng patients.

Polychlorinated biphenyl (PCB) poisonings occurred in western Japan, where it is called yusho, in 1968, and in central Taiwan, where it is called yu-cheng, in 1979. The average concentrations of PCBs in the adipose tissue, liver and blood of yusho patients and in the blood of yu-cheng patients were 1.9 ppm, 0.08 ppm, 6.7 ppb and 99 ppb, respectively. Seven PCB congeners, such as 2,4,5,3',4'-pentachloro-, 2,3,4,3',4'-pentachloro-, 2,4,5,2',4',5'-hexachloro-, 2,3,4,2',4',5'-hexachloro-, 2,3,4,5,3',4'-hexachloro-, 2,3,4,5,2',4',5'-heptachloro- and 2,3,4,5,2',3',4'-heptachloro biphenyls were identified in the blood and tissues of patients with yusho and yu-cheng and controls. The concentration of 2,3,4,5,3',4'-hexachlorobiphenyl was comparatively higher in the patients than in controls. The concentrations of polychlorinated dibenzofurans (PCDFs) in the adipose tissue and liver of yusho patients were 6 to 13 ppb and 3 to 25 ppb, respectively, while no PCDFs were detected in the controls. Major PCDF congeners identified in the tissues and blood of yusho and yu-cheng patients were the 2,3,6,8-tetrachloro-, 2,3,7,8-tetrachloro-, 1,2,4,7,8-pentachloro-, 2,3,4,7,8-pentachloro- and 1,2,3,4,7,8-hexachlorodibenzofurans (DFs), of which the 2,3,4,7,8-pentachloro compound was predominant. The concentrations of methylthio-PCB in the liver, lung and adipose tissue of yusho patients were 0.1 to 0.5, 0.2 to 1.4 and 0.5 to 1.0 ppb, respectively, and those of methysulfone PCBs were 0.3 to 0.7, 1.0 to 2.5 and 0.7 to 1.0 ppb, respectively. Some of the major peaks of the PCB methylthio and methylsulfone derivatives were identical in gas chromatographic retention times with those of 4-methylthio- and 4-methylsulfone-2,5,2',5'-tetrachlorobiphenyl PCDFs, especially 2,3,4,7,8-pentachloro DF, appear to be mainly responsible in the poisonings.

Benzofurans↗
PubMed1984

The effect of thyroid hormone on the high affinity Ca2+-ATPase in rat liver plasma membrane.

The effect of thyroid hormone on the high affinity Ca2+-ATPase activity in rat liver plasma membrane was studied. The high affinity Ca2+-ATPase activity in plasma membrane was activated by 10(-7)-10(-5) M of Ca2+ and was inhibited by 70 microM trifluoperazine. Thyroidectomy of rats was associated with an increase in the activity of high affinity Ca2+-ATPase. The increased enzyme activity was normalized by T4 administration to the animals. On the other hand, Na+-K+-ATPase activity in the membrane was decreased by thyroidectomy and the decreased enzyme activity was normalized by T4 administration. The results suggest that thyroid hormone inhibits the Ca2+ extrusion system by inhibiting calmodulin-independent high affinity Ca2+-ATPase in liver plasma membrane.

Animals↗
PubMed1984

Transient thyrotoxicosis after unilateral adrenalectomy in two patients with Cushing's syndrome.

We found transient hyperthyroidism in the course of hydrocortisone withdrawal in two patients who had undergone unilateral adrenalectomy to resect cortisol-hypersecreting adenoma. A 38-yr-old woman showed clinical thyrotoxicosis 3 months after the operation. Serum T4, T3 and TBG levels were 11.9 micrograms/dl, 310 ng/dl and 16.5 micrograms/ml, respectively. She was given methimazole (MMI) 15 mg/day for 4 weeks. After the cessation of MMI treatment, she eventually recovered to the euthyroid state. The other patient, a 34-yr-old man showed very mild clinical symptoms of hyperthyroidism 2 months after the operation. Serum T4, T3 and TBG levels were 10.4 micrograms/dl, 240 ng/dl and 14.5 micrograms/ml, respectively. In this case, no antithyroid drug was given. Two to three months after the onset of hyperthyroidism, he returned to the euthyroid state spontaneously. We carefully eliminated the possibility of factitious thyrotoxicosis in both cases. They had neither neck pain nor fever. Both had low radioactive iodine uptake by the thyroid. Therefore, we diagnosed them as painless thyroiditis induced after the resection of hypersecreting adrenal adenoma.

Adrenalectomy↗
PubMed1984

A case of hypokalemic myopathy associated with transient hypothyroidism.

A case of transient hypothyroidism in the course of hypokalemic myopathy is reported. A 69-year-old woman had severe muscle weakness and marked potassium deficiency associated with alkalosis during treatment with thiazide diuretics. The cause of muscle weakness proved to be hypokalemic myopathy confirmed by clinical findings and muscle biopsy. After the episode of hypokalemic myopathy, serum levels of thyroid hormone were lowered (T4; 3.8 micrograms/dl, T3; 54 ng/dl) and that of TSH was elevated (25.1 microU/ml). Antithyroid microsomal antibody was positive (1:25600) and anti-thyroglobulin antibody was negative. About one month after potassium supplement, her thyroid functions returned to normal, along with normalization of serum potassium level. This is the first documented case report of hypokalemic myopathy accompanied by transient hypothyroidism in a patient with autoimmune thyroiditis. We suggest that this transient hypothyroidism might be induced by hypokalemia during the course of autoimmune thyroiditis.

Aged↗
PubMed1983

[Effect of thyroid hormones on the beta-adrenergic receptor internalization in isolated rat hepatocytes].

The effect of the thyroid hormone(T4) on the internalization of beta-adrenergic receptors in isolated hepatocytes was examined. Uptake of [3H]-dihydroalprenolol(DHA) by the cells, which were prepared from untreated-rats, was increased by the time-dependent manner in vitro. The amount of incorporated-[3H]-DHA was decreased by further incubation in the presence of 10(-5) M of d, 1-isoproterenol. However, about 30% of incorporated-[3H]-DHA remained in the cells by this treatment. The amount of this [3H]-DHA remaining in the cells was lowered by pretreatment of the cells with methylamine, monodansylcadaverine, d, 1-isoproterenol or d, 1-propranolol. Then the amount of this [3H]-DHA was recognized as an internalized-receptor-hormone(or -DHA) complex. The total uptake(internalized- + membrane bound-) of [3H]-DHA by the cells was not significantly different between the thyroidectomized (TX + Saline) and T4-treated-thyroidectomized(TX + T4) rats. However, the rate of disappearance of incorporated-[3H]-DHA was greater in the TX + T4 animals compared to that in the TX + Saline animals. In the cells obtained from the TX + T4 animals, internalized-[3H]-DHA was significantly higher than that of the TX + Saline animals. The number of membrane associated beta adrenergic receptors was significantly lower in the TX + T4 group. These results suggest that the thyroid hormone induces an acceleration of internalization of beta adrenergic receptors in hepatocytes.

Alprenolol↗
PubMed1983

Evidence for the existence of protein inhibitors for S-adenosyl-L-methionine-mediated methylation of phosphatidylethanolamine in rat liver cytosol.

The effect of rat liver cytosol on phosphatidylcholine biosynthesis via the N-methylation of phosphatidylethanolamine has been studied. The purified rat liver plasma membrane was used as an enzyme source. The rat liver 105,000 x g supernatant(cytosol) contained two different inhibitors for S-adenosyl-L-methionine-mediated methylation of phosphatidylethanolamine to phosphatidyl-N-mono-methylethanolamine. The inhibitors were inactivated by pretreatment with trypsin or heating at 96 degrees C, but were not inactivated by RNase. The inhibitors did not inhibit the synthesis of phosphatidylcholine from phosphatidyl-N-mono-methylethanolamine. The results indicate that two different protein inhibitors for methylation are present in rat liver cytosol fraction and that the inhibition by these proteins may have a role for the regulation of phosphatidylcholine synthesis in the plasma membrane.

Animals↗
PubMed1981

[Laboratory and clinical evaluation of cefoxitin in children (author's transl)].

Pharmacokinetics of cefoxitin, a new injectable semisynthetic-cephamycin, was studied in 12 healthy children and also was studied cerebrospinal fluid levels in 1 patient with bacterial meningitis received 44.5 mg/kg of cefoxitin and thoracic fluid levels in 2 patients were measured. Cefoxitin was administered intravenously to 50 patients with various types of infections an average dose of 130 mg/kg/day for an average of 9 days. The results were as follows: 1. Favorable plasma levels were obtained comparing with those off conventional injectable cephalosporins after 15 mg/kg and 25 mg/kg of cefoxitin for one shot intravenous injection. The half lives of cefoxitin in the plasma were about 15.9 minutes up to 1 hour and 25.5 minutes up to 2 hours after an intravenous administration of cefoxitin at a dose of 15 mg/kg, and while, those were 15.9 minutes and 27.5 minutes after an intravenous administration of cefoxitin at a dose of 25 mg/kg, respectively. 2. Cefoxitin was excreted with high concentration up to 2 hours after the administration and thereafter, urinary concentration of cefoxitin declined rapidly with the lapse of time. The time course urinary concentration reflected those of plasma levels. Approximately 94.7% and 90.6% of dosed cefoxitin were recovered in the urine for 6 hours after the administration at the dose of 15 mg/kg and 25 mg/kg, respectively. 3. The cerebrospinal fluid levels of cefoxitin were only determined in a patient of bacterial meningitis. Therefore, further study should be performed. 4. The thoracic fluid levels with 2 patients were higher than cerebrospinal fluid levels. 5. Among the 50 patients with various infections, cefoxitin was clinically effective in 84% and bacterial response in 87%. 6. As adverse reactions, in total 79 patients included exclusive 29 patients, diarrhea occurred in 1 patient, sweating and cough in 1 patient, rash with fever in 4 patients, vascular pain in 2 patients, and leukopenia was observed in 1 patient, eosinophilia in 1 patient, and increase of GOT and LDH were observed in each 2 patients. The other adverse reactions were not experienced.

Adolescent↗
PubMed1980

Fluorimetric assay for ornithine decarboxylase by high-performance liquid chromatography.

A highly sensitive method for the assay of ornithine decarboxylase in sample solutions prepared from rat tissue homogenate is described which employs high-performance liquid chromatography with fluorescence detection. Putrescine formed from ornithine under the optimal conditions for the enzyme reaction is treated by Cellex P column chromatography for clean-up and converted into the fluorescamine derivative in the presence of cupric ion which inhibits the reaction of interfering amines with fluorescamine. The derivative is separated by reversed-phase chromatography on LiChrosorb RP-18 with linear gradient elution. The lower limit of detection for putrescine formed enzymatically is 5 pmol.

Animals↗
PubMed1979

High-performance liquid chromatographic determination of free and total polyamines in human serum as fluorescamine derivatives.

A highly sensitive and simple fluorimetric method for the determination of free and total polyamines, spermidine, spermine, putrescine and cadaverine, in human serum by high-performance liquid chromatography is described. The polyamines, obtained after clean-up of deproteinized serum by Cellex P column chromatography, are converted to their fluorescamine derivatives in the presence of nickel ion which inhibits the reaction of interfering amines with fluorescamine, and the derivatives are separated simultaneously by reversed-phase chromatography (LiChrosorb RP-18) with a linear gradient elution. The lower limits of detection are 10 and 15 pmole for spermine and the others in 0.5 ml of serum, respectively.

Adult↗