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Itaru YAMAMOTO, Takashi MIZUI, Yutaka NOGUCHI, Heitaroh IWATA
1978Volume 2Issue 1 Pages
1-11
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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Effects of intraperitoneal administrations of catecholamines, cyclic nucleotides and acetylcholine on 5- phosphoribosyl-1-pyrophosphate (PRPP)level in mouse liver have been investigated. ι-Epinephrine caused a marked increase in the level of PRPP, which was induced 5 to 10 min after the administration. ι-Phenylephrine and ι-norepinephrine showed moderate effects, while ι-isoproterenol gave no change of the PRPP level. The epinephrine-induced PRPP increase was completely blocked by the pretreatment of mice with α-adrenergic blocker, phenoxybenzamine, but not with β-blocker. Acetylcholine and carbachol also elevated the PRPP level in mouse liver, and this was inhibited by atropine pretreatment. In addition, both dibutyryl cyclic AMP and dibutyryl cyclic GMP significantly increased the liver PRPP level. There was a lag time of 5 to 10 min before induction of PRPP by dibutyryl cyclic AMP. Further experiments have to be taken in order to evaluate the role of cyclic nucleotides in the effect of catecholamin and acetylcholine on liver PRPP levels. In this report, we also discussed the role of PRPP in relation to a hyperuricemia induced by epinephrine.
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Yukio Yonetani, Mitsuo Ishii, Kazuko Yamada, Yasunao Ogawa
1978Volume 2Issue 1 Pages
13-30
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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The mechanisms of the actions of catecholamines on plasma purine catabolites were investigated in rats. The elevations of plasma levels of uric acid and allantoin were caused by two types of mechanisms which included either alpha or beta adrenoceptor-mediated actions. The effect, which was blocked by alpha adrenoceptor antagonist, could be mainly observed in the intraperitoneal treatment with epinephrine, norepinephrine or phenylephrin. e. These catecholamines obviously constricted the blood vessels of portal vein system, resulting in a marked increase of plasma purine catabolites in portal vein blood and a considerable reduction of ATP concentration in intestine and liver. The hepatic extracts prepared from animals administered epinephrine were studied on the amounts of adenine nucleotides, nucleosides and bases therein. The results showed the rapid break-down of hepatic ATP into the end product with a transient accumulation of 5' - AMP. On the other hand, the stimulation of purine catabolism mediated by beta adrenoceptor agonist was closely associated with the reduction of myocardial adenine nucleotides, which has been demonstrated by earlier workers. Isoproterenol caused the reduction of ATP concentration in the myocardium. However, neither compensatory increases of ADP and 5'-AMP nor recognizable amounts of nucleosides and bases were observed. The reduced amounts of myocardial adenine nucleotides by isoproterenol corresponded well to the increased amounts of plasma purine catabolites. Our present studies supported that a rapid breakdown of tissue adenine nucleotides should be more essential action of catecholamine on the increase of plasma purine catabolites, although earlier workers have suggested that catecholamine might induce hyperuricemia by promotion of xanthine oxidase reaction or its renal vasoconstricting action.
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Yukio Yonetani, Mitsuo Ishii, Kazuko Yamada, Yasunao Ogawa
1978Volume 2Issue 1 Pages
31-46
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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Possible role of catecholamine in a pathogenesis of hyperuricemia was studied in rats and chickens. Although elevation of plasma purine catabolites induced by catecholamine was acute and transient, the action of catecholamine should be taken into consideration for the cause of hyperuricemia. Actually, catecholamine caused prolonged elevation of plasma purine catabolites in rats under severe excretory disturbance by ligating ureters. However, no prolongation of the effect was observed in the animals with lighter degree of excretory disorders. A high correlation between the concentrations of serum uric acid and serum creatinine in hyperuricemic sportsmen has been reported recently. In our experiments in rats, beta adrenoceptor agonists reduced myocardial high-energy phosphate compounds, resulting in highly correlated increases of plasma purine catabolites and plasma creatinine. The rats received stress by fixing showed marked increase of plasma purine catabolites. The increase was inhibited by the pretreatment of sedatives and reserpine, and was partially blocked by adrenoceptor antagonists.These results supported that the increase of plasma purine catabolites might be caused by endogenous catecholamine released by the stress. Successive administrations of catecholamine failed to maintain higher concentration of plasma purine catabolites. However, the effect of beta adrenoceptor agonists on plasma purine catabolites was obviously potentiated by the pretreatment with aminophylline or 11-deoxycorticosterone acetate (DOCA) in rats. Such a potentiation was also observed in chickens, resulting in an abnormally high concentration of plasma uric acid. The chickens received catecholamine together with DOCA under salt-loading showed a remarkable hyperuricemia subjecting to deposition of uric acid in and/or around their organs and tissues. From the results described above, it could be concluded that catecholamine should play a significant role in the induction of hyperuricemia under the specific conditions.
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
1978Volume 2Issue 1 Pages
47-58
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1978Volume 2Issue 1 Pages
59-61
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese]
1978Volume 2Issue 1 Pages
63-68
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1978Volume 2Issue 1 Pages
69-70
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese]
1978Volume 2Issue 1 Pages
71-72
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1978Volume 2Issue 1 Pages
73-84
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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Toshiro TANGO, Tsuguchika KAMINUMA, Kusuki NISHIOKA, Kiyonobu MIKANAGI
1978Volume 2Issue 1 Pages
85-88
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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The analysis of familial ag g r e gation was carried out on the residents in Tooshi island, Mie prefecture, closed community in which outdoor environmental factors are expected to be uniform. The standardized serum uric acid value called “normal quotient” of serum uric acid value were used for the sake of comparative study. This study suggests that gene action may be caused by so called polygene system. In addition to polygenic inheritance, the value of serum uric acid is also influenced by the interaction of genetic and environmental factors. In the parent-chi l d r en analysis, the most consistent relationship was. found in mother and child. There was no significant aggregation of serum uric acid values between spouses, although there was very significant aggregation between siblings. The extent of aggregation of serum uric acid values between siblings was not significantly different from that of mother and child. Consequently, our present study lends further weight to the view that serum uric acid values are influenced mainly by mothers' genetic factors.
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[in Japanese], [in Japanese], [in Japanese]
1978Volume 2Issue 1 Pages
99-110
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1978Volume 2Issue 1 Pages
111-115
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1978Volume 2Issue 1 Pages
117-124
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese], [in Japanese]
1978Volume 2Issue 1 Pages
125-130
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1978Volume 2Issue 1 Pages
131-132
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese]
1978Volume 2Issue 1 Pages
133-139
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
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[in Japanese], [in Japanese], [in Japanese]
1978Volume 2Issue 1 Pages
141
Published: August 21, 1978
Released on J-STAGE: November 27, 2012
JOURNAL
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