Kugimiya T, Fujisawa M, Suwa K, Yamamura H, Minohara K, Kasama T
Tohoku J Exp Med. 1982 Jan;136(1):35-41. doi: 10.1620/tjem.136.35.
Effects of ortho-iodo-sodium benzoate (OISB) on oxygen-hemoglobin affinity were studied in unanesthetized beagles with simultaneous measurement of its plasma concentrations. Oxygen-hemoglobin affinity changes correlated well with the plasma concentrations of the drug. Intravenous administration of 100 mg/kg of OISB increased P50 significantly from the control value of 28.6 +/- 0.8 mmHg to 29.5 +/- 0.7 mmHg and 30.0 +/- 0.5 mmHg, 5 min and 30 min after the infusion, respectively. P50 gradually decreased thereafter, and after 1 hr period, elevation was no longer significant. Administration of 200 mg/kg of OISB caused a significant increase in P50 from the control of 29.3 +/- 0.3 mmHg to 30.5 +/- 0.4 mmHg, 31.1 +/- 0.3 mmHg, 31.1 +/- 0.3 mmHg and 30.5 +/- 0.5 mmHg, at 5 min, 30 min, 1 hr and 3 hr, respectively. P50 elevation declined thereafter to control levels. Plasma concentrations of the drug reached its highest level 5 min after the administration and declined gradually thereafter. All significant elevations of P50 were accompanied by the plasma concentrations of the drug more than 200 micrograms/ml. Biological half-life of the drug was found to be about 5.5 hr.
在未麻醉的比格犬中研究了邻碘苯甲酸钠(OISB)对氧合血红蛋白亲和力的影响,并同时测定其血浆浓度。氧合血红蛋白亲和力的变化与药物的血浆浓度密切相关。静脉注射100mg/kg的OISB后,输注后5分钟和30分钟时,P50分别从对照值28.6±0.8mmHg显著升高至29.5±0.7mmHg和30.0±0.5mmHg。此后P50逐渐下降,1小时后升高不再显著。注射200mg/kg的OISB导致P50在5分钟、30分钟、1小时和3小时时分别从对照值29.3±0.3mmHg显著升高至30.5±0.4mmHg、31.1±0.3mmHg、31.1±0.3mmHg和30.5±0.5mmHg。此后P50升高降至对照水平。药物血浆浓度在给药后5分钟达到最高水平,此后逐渐下降。所有P50的显著升高都伴随着药物血浆浓度超过200μg/ml。发现该药物的生物半衰期约为5.5小时。