a Department of Biomedical Sciences , University of Minnesota, Medical School , Duluth , MN , USA.
J Immunotoxicol. 2017 Dec;14(1):235-240. doi: 10.1080/1547691X.2017.1394934.
Preeclampsia is a pregnancy-specific condition manifested by new-onset maternal hypertension with systemic inflammation, including increased innate immune system complement activation. While exact pathophysiology is unknown, evidence suggests that inadequate spiral artery invasion and resulting utero-placental insufficiency is the initiating event. Cigarette smoking during pregnancy decreases the risk of preeclampsia. Nicotine, a major component of cigarettes, stimulates the efferent cholinergic anti-inflammatory pathway through peripherally expressed nicotinic acetylcholine receptors (nAChR) and is known to attenuate ischemia-reperfusion injury in kidney and liver. Prior studies indicated that complement activation was critical for placental ischemia-induced hypertension in a rat model. Thus, it was hypothesized here that nicotine was responsible for the protective effect of cigarette smoking in preeclampsia and would attenuate placental ischemia-induced systemic complement activation and hypertension. The Reduced Utero-placental Perfusion Pressure (RUPP) model in the pregnant rat was employed to induce placental ischemia, resulting in complement activation, fetal resorptions, and hypertension. On gestation day (GD)14, nicotine (1 mg/kg) or saline was administered via subcutaneous injection prior to RUPP surgery and daily through GD18. On GD19, placental ischemia significantly increased mean arterial pressure (MAP) in saline injected animals. However, the placental ischemia-induced increase in blood pressure was not evident in nicotine-treated animals and nicotine treatment significantly increased MAP variability. Circulating C3a was measured as an indicator of complement activation and increased C3a in RUPP compared to Sham persisted with nicotine treatment, as did fetal resorptions. These data suggested to us that nicotine may contribute to the decreased risk of preeclampsia with cigarette smoking, but this protective effect was confounded by additional effects of nicotine on the cardiovascular system.
子痫前期是一种妊娠特有的疾病,表现为新发生的母体高血压伴全身炎症,包括固有免疫系统补体激活增加。虽然确切的病理生理学机制尚不清楚,但有证据表明,螺旋动脉侵袭不足和由此导致的子宫胎盘功能不全是起始事件。怀孕期间吸烟可降低子痫前期的风险。香烟中的主要成分尼古丁通过外周表达的烟碱型乙酰胆碱受体(nAChR)刺激传出胆碱能抗炎途径,已知可减轻肾和肝的缺血再灌注损伤。先前的研究表明,补体激活对于大鼠模型中胎盘缺血引起的高血压至关重要。因此,这里假设尼古丁是香烟吸烟预防子痫前期的保护作用的原因,并会减轻胎盘缺血引起的全身补体激活和高血压。在妊娠大鼠中采用减少子宫胎盘灌注压(RUPP)模型诱导胎盘缺血,导致补体激活、胎儿吸收和高血压。在妊娠第 14 天(GD14),通过皮下注射在 RUPP 手术前和 GD18 期间给予尼古丁(1mg/kg)或盐水。在 GD19 时,与盐水注射动物相比,胎盘缺血显着增加了平均动脉压(MAP)。然而,在尼古丁处理的动物中,胎盘缺血引起的血压升高并不明显,并且尼古丁处理显着增加了 MAP 变异性。循环 C3a 被测量为补体激活的指标,与假手术相比,RUPP 中的 C3a 增加,并且在用尼古丁处理时持续存在,胎儿吸收也是如此。这些数据表明,尼古丁可能有助于降低吸烟引起的子痫前期风险,但这种保护作用因尼古丁对心血管系统的其他影响而复杂化。