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ATRAZINE INCREASES THE SODIUM ABSORPTION IN FROG (RANA ESCULENTA) SKIN

机译:Atrazine增强Frog(毛细血管)皮肤中钠的吸收

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The presence of atrazine in agricultural sites has been linked to the decline in amphibian populations. The efforts of the scientific community generally are directed toward investigating the long-term effect of atrazine on complex functions (reproduction or respiration), but in the present study, we investigated the short-term effect on the short-circuit current (I_(SC)), a quantitative measure of the ion transport operated by frog (Rana esculenta) skin. Treatment with 5 μM atrazine (1.08 mg/L) does not affect the transepithelial outfluxes of [~(14)C]mannitol or [~(14)C]urea; therefore, atrazine does not damage the barrier properties of frog skin. Atrazine causes a dose-dependent increase in the short-circuit current, with a minimum of 4.64 ±0.76 μA/cm~2 (11.05% ± 1.22%) and a maximum of 12.7 ± 0.7 μA/cm~2 (35% ± 2.4%) measured at 10 nM and 5 μM, respectively. An increase in I_(SC) also is caused by 5 μM ametryne, prometryn, simazine, terbuthylazine, or terbutryn (other atrazine derivatives). In particular, atrazine increases the transepithelial ~(22)Na~+ influx without affecting the outflux. Finally, stimulation of I_(SC) by atrazine is suppressed by SQ 22536, H89, U73122, 2-aminoethoxydiphenyl borate, and W7 (blockers of adenylate cyclase, protein kinase A, phospholipase C, intracellular Ca~(2+) increase, and calmodulin, respectively), whereas indomethacin and calphostin C (inhibitors of cyclooxygenase and protein kinase C, respectively) have no effect.
机译:农业场所中at去津的存在与两栖动物种群的减少有关。科学界的努力通常旨在研究of去津对复杂功能(繁殖或呼吸)的长期影响,但在本研究中,我们研究了对短路电流的短期影响(I_(SC )),定量测量青蛙(Rana esculenta)皮肤的离子迁移。用5μM阿特拉津(1.08 mg / L)处理不会影响[〜(14)C]甘露醇或[〜(14)C]尿素的经上皮流出。因此,阿特拉津不会破坏青蛙皮肤的阻隔性能。 r去津引起短路电流的剂量依赖性增加,最小值为4.64±0.76μA/ cm〜2(11.05%±1.22%),最大值为12.7±0.7μA/ cm〜2(35%±2.4) %)分别在10 nM和5μM下测得。 I_(SC)的增加也由5μM的metry紫草素,前萘啶,西咪嗪,叔丁嗪或叔丁烯(其他at去津衍生物)引起。特别地,at去津增加了跨上皮的〜(22)Na〜+流入,而没有影响流出。最后,SQ 22536,H89,U73122、2-氨基乙氧基二苯基硼酸酯和W7抑制了阿特拉津对I_(SC)的刺激(腺苷酸环化酶,蛋白激酶A,磷脂酶C,细胞内Ca〜(2+)的阻滞剂增加,并且钙调蛋白),消炎痛和钙磷蛋白C(分别为环氧合酶和蛋白激酶C的抑制剂)无效。

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