Ramos K S, Thurlow C H
Department of Physiology and Pharmacology, College of Veterinary Medicine, Texas A&M University, College Station 77843-4466.
J Toxicol Environ Health. 1993 Sep;40(1):61-76. doi: 10.1080/15287399309531776.
The present studies were designed to compare the acute cytotoxic responses of cultured avian and rodent aortic smooth muscle cells (SMCs) to allylamine (AAM), a selective vascular toxin. SMCs were isolated from male Japanese quail or Sprague-Dawley rats and established in culture by standard procedures. Cellular glutathione (GSH) content and lactate dehydrogenase (LDH) leakage were used as indices of cytotoxicity. Exposure of avian and rodent SMCs in primary culture to AAM (0.2-200 microM) for 4 h was associated with a significant reduction in cellular GSH and enzyme leakage in cultures of both cell types. Increased exposure time to 24 h further depleted cellular GSH levels and enhanced the leakage of LDH in primary cultures of avian SMCs. In contrast, enhanced LDH leakage occurred without further GSH depletion in primary cultures of rodent SMCs upon exposure to AAM for 24 h. Removal of serum did not modulate the cytotoxic response profile of primary cultures of avian SMCs treated with 200 microM AAM, but was associated with marked elevation in cellular GSH levels and significant LDH leakage in rodent SMC cultures. The cytotoxic responses to 0.2-200 microM AAM in secondary cultures of avian SMCs were comparable to those observed in primary culture. In contrast, AAM-induced enzyme leakage did not consistently correlate with changes in GSH content in subcultured rodent SMCs. Challenge with 200 microM acrolein (ACR) for 4 h reduced the GSH content in avian, but not rodent, subcultures of SMCs. However, significant LDH leakage occurred in subcultures of both cell types upon exposure to ACR. Although hydrogen peroxide (H2O2) did not modulate GSH levels in avian or rodent cultures, leakage of LDH was observed in rat SMCs challenged with 200 microM H2O2. Removal of serum did not alter the cytotoxic responses of avian subcultures to 200 microM AAM for 24 h, but fully prevented cytotoxicity in rodent subcultures. These data suggest that potentially significant variations in the sequence of events leading to injury may exist between quail and rat aortic SMCs. These differences may contribute to the enhanced avian susceptibility to AAM-induced aortic injury in vivo.
本研究旨在比较培养的禽类和啮齿类动物主动脉平滑肌细胞(SMC)对烯丙胺(AAM,一种选择性血管毒素)的急性细胞毒性反应。从雄性日本鹌鹑或Sprague-Dawley大鼠中分离出SMC,并通过标准程序进行培养。细胞内谷胱甘肽(GSH)含量和乳酸脱氢酶(LDH)泄漏用作细胞毒性指标。将原代培养的禽类和啮齿类动物SMC暴露于AAM(0.2 - 200微摩尔)4小时,两种细胞类型的培养物中细胞内GSH均显著降低,且酶泄漏增加。将暴露时间延长至24小时,禽类SMC原代培养物中细胞内GSH水平进一步降低,LDH泄漏增加。相比之下,啮齿类动物SMC原代培养物暴露于AAM 24小时后,LDH泄漏增加,但细胞内GSH没有进一步消耗。去除血清并未调节用200微摩尔AAM处理的禽类SMC原代培养物的细胞毒性反应,但与啮齿类动物SMC培养物中细胞内GSH水平显著升高和LDH明显泄漏有关。禽类SMC传代培养物对0.2 - 200微摩尔AAM的细胞毒性反应与原代培养中观察到的反应相当。相比之下,AAM诱导的啮齿类动物传代培养SMC中酶泄漏与GSH含量变化并不始终相关。用200微摩尔丙烯醛(ACR)刺激4小时可降低禽类但不降低啮齿类动物SMC传代培养物中的GSH含量。然而,两种细胞类型的传代培养物暴露于ACR后均出现显著的LDH泄漏。虽然过氧化氢(H2O2)未调节禽类或啮齿类动物培养物中的GSH水平,但用200微摩尔H2O2刺激大鼠SMC时观察到LDH泄漏。去除血清并未改变禽类传代培养物对200微摩尔AAM 24小时的细胞毒性反应,但完全防止了啮齿类动物传代培养物中的细胞毒性。这些数据表明,鹌鹑和大鼠主动脉SMC在导致损伤的事件顺序上可能存在潜在的显著差异。这些差异可能导致禽类在体内对AAM诱导的主动脉损伤更易感性增加。