Randell Amy, Daneshtalab Noriko
300 Prince Philip Drive, Health Sciences Center, Memorial University of Newfoundland, School of Pharmacy, St. John's, Newfoundland A1B 3V6, Canada.
300 Prince Philip Drive, Health Sciences Center, Memorial University of Newfoundland, School of Pharmacy, St. John's, Newfoundland A1B 3V6, Canada.
Life Sci. 2016 Apr 15;151:15-22. doi: 10.1016/j.lfs.2016.02.012. Epub 2016 Feb 21.
Patients with rheumatoid arthritis (RA), have a higher incidence of hypertension and stroke than the normal population. Currently there exists no animal model to study the pathogenic interactions of hemorrhagic stroke (HS) subsequent to chronic inflammation and hypertension. We have created and defined a hypertensive-mono-arthritic animal model who demonstrate gros signs of cerebral hemorrhage in presence of mono-arthritis.
Spontaneously hypertensive rats (SHR) were fed either a high salt diet (4% NaCl; HSD) or Purina chow (RD) from weaning. Complete Freund's adjuvant (CFA) was injected into the left hind paw at 21-28weeks (control groups received saline (SAL)). Degree of inflammation, joint swelling, weight and blood pressure were monitored for 21days. Animals were then sacrificed and their brain and left hind paw evaluated.
All groups were hypertensive throughout the experimental period (>180mmHg systolic), irrespective of diet. Both CFA groups produced significant local inflammatory response in their injected paw with associated joint degradation and cellular infiltrates. Systemic plasma TNF-α levels were significantly elevated in CFA groups, with significant increase in TNF-α at 7 and 14days, compared to SAL groups. Cerebral hemorrhage was visualized in the CFA groups but not SAL controls, with a higher severity in HSD-CFA group.
The mono-arthritic hypertensive animals are capable of developing HS upon induction of inflammatory insult. The HSD appears to exacerbate the inflammatory response and influence degree of the hemorrhage. Our novel, multi-disease model may provide an appropriate platform to study the pathogenesis of HS among arthritic patients.
类风湿性关节炎(RA)患者患高血压和中风的发生率高于正常人群。目前尚无动物模型可用于研究慢性炎症和高血压后继发性出血性中风(HS)的致病相互作用。我们创建并定义了一种高血压单关节炎动物模型,该模型在患单关节炎时会出现脑出血的明显迹象。
自断奶起,将自发性高血压大鼠(SHR)分别喂食高盐饮食(4%氯化钠;HSD)或普瑞纳饲料(RD)。在21至28周时,将完全弗氏佐剂(CFA)注射到左后爪(对照组注射生理盐水(SAL))。在21天内监测炎症程度、关节肿胀、体重和血压。然后处死动物,对其大脑和左后爪进行评估。
在整个实验期间,所有组均为高血压(收缩压>180mmHg),与饮食无关。两个CFA组在注射爪中均产生了显著的局部炎症反应,并伴有相关的关节退化和细胞浸润。与SAL组相比,CFA组的全身血浆TNF-α水平显著升高,在第7天和第14天TNF-α显著增加。在CFA组中观察到脑出血,而SAL对照组未观察到,HSD-CFA组的脑出血严重程度更高。
单关节炎高血压动物在受到炎症刺激后能够发生HS。HSD似乎会加剧炎症反应并影响出血程度。我们的新型多疾病模型可能为研究关节炎患者中HS的发病机制提供一个合适的平台。