Ueno A, Tanaka K, Katori M, Hayashi M, Arai Y
Prostaglandins. 1981 Apr;21(4):637-48. doi: 10.1016/0090-6980(81)90012-5.
The activity of synthetic LTC4 was tested in guinea-pig ileum and was 200 times more potent than histamine in contraction of the ileum (3 x 10(-11) M- 3 x 10(-9) M). The activities of LTC4 and LTD4 in increased vascular permeability in guinea pigs, rats and rabbits were compared with those of histamine, bradykinin and prostaglandin (PG) E2. LTC4 was approximately equipotent to bradykinin on a molar basis in guinea pigs and rats and 5-100 times more potent than histamine. LTD4 was about 10 times more potent than LTC4 in guinea pigs and was equipotent to LTC4 in rats. On the contrary, in rabbits, neither LTC4 (up to 30 nmole/site) nor LTD4 (1 nmole/site) induced the dye exudation. These results show that species difference is present in activity of LTC4 and LTD4 in vascular permeability. Furthermore, in guinea pigs, the vascular permeability increased by LTC4 was not affected after pretreatment with pyrilamine (2.5 mg/kg, i.v.), and LTC4 and LTD4 did not potentiate the activity of bradykinin in vascular permeability.
合成白三烯C4(LTC4)在豚鼠回肠中的活性进行了测试,其在回肠收缩方面的效力比组胺高200倍(3×10⁻¹¹M - 3×10⁻⁹M)。将LTC4和白三烯D4(LTD4)在豚鼠、大鼠和兔子中增加血管通透性的活性与组胺、缓激肽和前列腺素(PG)E2的活性进行了比较。在豚鼠和大鼠中,按摩尔计算,LTC4与缓激肽的效力大致相当,且比组胺强5 - 100倍。在豚鼠中,LTD4的效力比LTC4约强10倍,在大鼠中与LTC4效力相当。相反,在兔子中,LTC4(高达30 nmol/部位)和LTD4(1 nmol/部位)均未引起染料渗出。这些结果表明,LTC4和LTD4在血管通透性方面的活性存在种属差异。此外,在豚鼠中,用吡苄明(2.5 mg/kg,静脉注射)预处理后,LTC4增加的血管通透性不受影响,并且LTC4和LTD4在血管通透性方面不会增强缓激肽的活性。