Effect Of Aspirin On The Production Of PGI2 By Various Blood Vessels And Mda By Platelets

1981 ◽  
Author(s):  
M Takada ◽  
H Tsukada ◽  
H Tanaka ◽  
H Gonmori ◽  
N Kobayashi ◽  
...  

This study was desinged to determine whether the differential inhibition of prostacyclin(PGI2) production by vessel wall and malondialdehyde(MDA) production by platelet might be possible by oral administration of aspirin(ASA). Rabbits weghing 2-3kg were used. MDA production by platelet was measured by the Stuart’s method with minor modification. The PGI2 production by vessel wall was assessed by the Moncada’s method with minor modification.The PGI2 production by caval vein, pulmonary artery, pulmonary vein,femoral artery, femoral vein and coronary artery was 148±55%, 136±56%, 153±55%, 134±56%, 123±64%, 103±55% to that of aorta, respectively. The PGI2 production by these vessels was inhibited to 20-40% to their initial level 6h after the single oral administration of 0.3g ASA, and restored to the initial level by 24h, while the MDA production was inhibited more conspicuously and remained at less than 50% of the initial level even 48h.The effect of daily oral administration of ASA on production of PGI2 by aorta and MDA by platelet was investigated. PGI2 production was suppressed to about 10% of the initial level 24h after the last dose of 3 to 7 daily administration of 0,3g of ASA. This indicates that the daily ASA administration results in the cummulative inhibition of PGI2 production. On the other hand, when administered every other day, the same amount of ASA exerted significantly less inhibition of PGI2 production, being at about 50% of initial level 24h after the last dose. MDA production was nearly completely inhibited over the observation periods.These results suggests that the differential inhibition of vascular PGI2 production and platelet aggregation may be possible by the administration of ASA at an appropriate amount and proper interval.

2009 ◽  
Vol 102 (2) ◽  
pp. 242-248 ◽  
Author(s):  
Takashi Hashimoto ◽  
Yoshiaki Ozaki ◽  
Mayuko Taminato ◽  
Swadesh K. Das ◽  
Masashi Mizuno ◽  
...  

The pharmacokinetics of dietary fucoxanthin, one of the xanthophylls in brown sea algae, is little understood. In the present study, mice were orally administered fucoxanthin, and the distribution and accumulation of fucoxanthin and its metabolites fucoxanthinol and amarouciaxanthin A were measured in the plasma, erythrocytes, liver, lung, kidney, heart, spleen and adipose tissue. In a single oral administration of 160 nmol fucoxanthin, fucoxanthinol and amarouciaxanthin A were detectable in all specimens tested in the present study, but fucoxanthin was not. The time at maximum concentration (Tmax) of these metabolites in adipose tissue was 24 h, while the Tmax in the others was 4 h. The area under the curve to infinity (AUC∞) of fucoxanthinol in the liver was the highest value (4680 nmol/g × h) among the tissues tested in the present study, while the AUC∞ of amarouciaxanthin A in adipose tissue was the highest value (4630 nmol/g × h). In daily oral administration of 160 nmol fucoxanthin for 1 week, fucoxanthin was also detectable in the tissues even at a low concentration. The amount of fucoxanthinol was 123 nmol/g in the heart and 85·2 nmol/g in the liver. Amarouciaxanthin A in the adipose tissue was distributed at a concentration of 97·5 nmol/g. These results demonstrate that dietary fucoxanthin accumulates in the heart and liver as fucoxanthinol and in adipose tissue as amarouciaxanthin A.


1988 ◽  
Vol 59 (3) ◽  
pp. 509-518 ◽  
Author(s):  
M. Hidiroglou ◽  
K. Karpinski

1. Increases in plasma tocopherol concentrations were compared in sheep after a single oral administration of (per kg body-weight): 67 mg D- and 91 mg DL-epimers of α-tocopherol, and 74 mg D- and 100 mg DL-epimers of α-tocopheryl acetate, or intravenous administration of DL-α-tocopherol and DL-epimers of DL-α-tocopheryl acetate.2. The results showed that biological availability was higher after D-α-tocopherol dosing than after the other forms. Intravenous administration of D-α-tocopherol acetate was a more effective way of dosing in sheep than equivalent intravenous amounts of DL-α-tocopheryl acetate or DL-α-tocopherol.


1984 ◽  
Vol 107 (2) ◽  
pp. 275-281 ◽  
Author(s):  
Roland De Coster ◽  
Dominiek Beerens ◽  
Jef Dom ◽  
Gustaaf Willemsens

Abstract. Some endocrinological effects of single daily oral administration of 150 mg ketoconazole for 15 days were investigated in 4 male beagle dogs. Plasma testosterone fell markedly within 3–4 h and then progressively returned to control concentrations by 10 h after drug administration. On the other hand, plasma 17α-hydroxyprogesterone, progesterone and 17α,20α-dihydroxyprogesterone increased within 3–10 h before returning to basal values after 24 h. Plasma LH did not rise significantly though some high individual levels were noted. Plasma cortisol and oestradiol-17α levels were not significantly modified by the treatment. These results confirm that a high therapeutic dose of ketoconazole, given orally once a day, transiently inhibits in vivo the 17–20 lyase enzyme of the testis, without modifying basal cortisol and oestradiol-17β plasma concentrations and that enzymatic inhibition still occurs after daily treatment for up to 2 weeks but remains transient and parallels the resorption profile of the drug so that normal plasma testosterone levels are observed from 10 to 24 h after drug intake. However, permanent inhibition of androgen biosynthesis might be obtained by the administration of high doses of ketoconazole given several times a day.


1993 ◽  
Vol 24 (1) ◽  
pp. 143-145 ◽  
Author(s):  
Yoshiaki Akimoto ◽  
Yoshiko Mochizuki ◽  
Akio Uda ◽  
Hiroaki Omata ◽  
Sumio Saito ◽  
...  

1978 ◽  
Vol 19 (4) ◽  
pp. 561-568 ◽  
Author(s):  
Nils E. Søli ◽  
Inger Nafstad

Perfusion ◽  
2010 ◽  
Vol 25 (3) ◽  
pp. 147-152 ◽  
Author(s):  
Vladimir Svitek ◽  
Vladimir Lonsky ◽  
Faraz Anjum

Cardiotomy suction is used for preservation of autologous blood during on-pump cardiac surgery at present. Controversially, the exclusion of cardiotomy suction in some types of operations (coronary artery bypass surgery) is not necessarily associated with an increased transfusion requirement. On the other hand, the use of cardiotomy suction causes an amplification of systemic inflammatory response and a resulting coagulopathy, as well as exacerbation of the microembolic load and hemolysis. This leads to a tendency towards increased blood loss, transfusion requirement and organ dysfunction. On the basis of these facts, it is appropriate to reconsider routine use of cardiotomy suction in on-pump coronary artery surgery.


1990 ◽  
Vol 183 (5) ◽  
pp. 1846-1847
Author(s):  
C.D. Evans ◽  
G.D. Jones ◽  
V. Facchini ◽  
J. McEwen ◽  
Y. Yeang

2011 ◽  
Vol 168 (16) ◽  
pp. 431-431
Author(s):  
G. J. B. Ladaga ◽  
F. P. Lezica ◽  
A. M. Barboni ◽  
J. A. Picos ◽  
G. A. de Erausquin

2011 ◽  
Vol 50 (03) ◽  
pp. 243-247
Author(s):  
Ioannis Niopas ◽  
Athanasios Daftsios ◽  
Ioannis Xanthakis ◽  
Nicolaos Nikolaidis ◽  
Samuel Njau

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