Nakatsuji K, Kii Y, Fujitani B, Ito T
Research Laboratories, Dainippon Pharmaceutical Co., Ltd., Osaka, Japan.
Arzneimittelforschung. 1990 Feb;40(2 Pt 1):218-25.
The effects of recombinant human Tumor Necrosis Factor (rHu-TNF, PT-050), an antitumor agent, on the cardiovascular, gastrointestinal, renal and blood functions were examined in experimental animals. 1. PT-050 at 10(5) U/kg i.v. did not affect blood pressure and blood flow in anesthetized dogs. However, these were decreased 2-3 h after i.v. injection of 10(6) U/kg. A sustained decrease in blood pressure was seen in conscious dogs. PT-050 decreased systolic blood pressure and increased heart rate with a peak at 5-7 h after administration of 10 micrograms/kg (2.55 x 10(4) U/kg) i.v. and 10(5) U/kg s.c. PT-050 was without effect on perfusion volume in rabbit ear vessel preparations. 2. PT-050 enhanced gastric emptying in rats and intestinal charcoal meal propulsion in mice at 10(6) and 10(7) U/kg s.c., respectively. It decreased gastric juice volume and acid content with an increase of gastric juice pH in pyrolus ligated rats at 10(6) U/kg s.c. 3. PT-050 caused diarrhea at 10(5) U/kg i.v. in mice, while at 10(7) U/kg s.c., it did not exert the effect. 4. PT-050 increased urine volume and Na+ excretion at 3 x 10(3) U/kg i.v. and 10(5) U/kg s.c. in saline-loaded rats. 5. PT-050 decreased platelet counts at 10(5) U/kg i.v., depressed platelet aggregation responses to collagen and ADP at 10(6) U/kg i.v., and prolonged APTT and PT at 3 x 10(5) U/kg i.v. in rats, although it neither affected platelet aggregation nor blood coagulation in vitro. PT-050 neither affected platelet counts at 10(5) U/kg s.c., nor platelet aggregation at 10(7) U/kg s.c.(ABSTRACT TRUNCATED AT 250 WORDS)
在实验动物中研究了抗肿瘤药物重组人肿瘤坏死因子(rHu-TNF,PT-050)对心血管、胃肠道、肾脏和血液功能的影响。1. 静脉注射10(5) U/kg的PT-050对麻醉犬的血压和血流无影响。然而,静脉注射10(6) U/kg后2 - 3小时,血压和血流降低。清醒犬出现血压持续下降。静脉注射10微克/千克(2.55 x 10(4) U/kg)和皮下注射10(5) U/kg的PT-050后,收缩压降低,心率增加,在给药后5 - 7小时达到峰值。PT-050对兔耳血管制剂的灌注量无影响。2. 皮下注射10(6)和10(7) U/kg的PT-050分别增强大鼠的胃排空和小鼠的肠炭末推进。皮下注射10(6) U/kg的PT-050可减少幽门结扎大鼠的胃液体积和酸含量,同时增加胃液pH值。3. 静脉注射10(5) U/kg的PT-050可使小鼠腹泻,而皮下注射10(7) U/kg则无此作用。4. 静脉注射3 x 10(3) U/kg和皮下注射10(5) U/kg的PT-050可使盐水负荷大鼠的尿量和Na+排泄增加。5. 静脉注射10(5) U/kg的PT-050可降低大鼠血小板计数,静脉注射10(6) U/kg可抑制血小板对胶原和ADP的聚集反应,静脉注射3 x 10(5) U/kg可延长大鼠的活化部分凝血活酶时间(APTT)和凝血酶原时间(PT);尽管PT-050在体外对血小板聚集和血液凝固均无影响。皮下注射10(5) U/kg的PT-050对血小板计数无影响,皮下注射10(7) U/kg对血小板聚集也无影响。(摘要截断于250字)