McFarlane D, Holbrook T C
Department of Physiological Sciences, Oklahoma State University, Stillwater, OK 74078, USA.
J Vet Intern Med. 2008 Mar-Apr;22(2):436-42. doi: 10.1111/j.1939-1676.2008.0076.x.
Equine pituitary pars intermedia dysfunction (PPID) is the result of a loss of dopaminergic inhibition of the pars intermedia secondary to neurodegeneration of periventricular hypothalamic neurons. The pathologic events contributing to development of neurodegeneration or clinical signs in equids with PPID are unknown. Chronic inflammation may contribute to initiation or progression of PPID.
Horses with PPID have a distinct systemic cytokine profile compared with that of normal adult or aged horses. The cytokine profile of healthy aged horses differs from that of adult horses.
Aged horses with PPID, healthy aged-matched controls, and adult controls (n = 14 per group).
Total leukocyte cytokine expression was determined by quantitative polymerase chain reaction (PCR), and tumor necrosis factor (TNF)-alpha plasma concentration was determined by enzyme-linked immunosorbent assay (ELISA). Peripheral blood mononuclear cell (PBMC) TNF-alpha response after endotoxin (lipopolysaccharide [LPS]) treatment was assessed by ELISA.
Aged healthy horses had increased expression of interleukin (IL)-6, IL-8, and interferon-gamma as well as PBMC TNF-alpha release after LPS stimulation compared with healthy adult horses. In contrast, aged horses with PPID had increased IL-8 expression, but expression of other cytokines was similar to that of healthy adult horses, not age-matched controls.
Aged horses show evidence of a proinflammatory state that may contribute to development of age-associated diseases. Horses with PPID have increased expression of IL-8, which may influence the ability of horses with PPID to respond to bacterial pathogens. The general decrease in proinflammatory cytokine expression observed in horses with PPID may be the outcome of high plasma concentrations of anti-inflammatory hormones.
马垂体中间叶功能障碍(PPID)是室周下丘脑神经元神经变性继发的垂体中间叶多巴胺能抑制丧失的结果。导致患有PPID的马发生神经变性或临床症状的病理事件尚不清楚。慢性炎症可能促成PPID的起始或进展。
与正常成年马或老龄马相比,患有PPID的马具有独特的全身细胞因子谱。健康老龄马的细胞因子谱与成年马不同。
患有PPID的老龄马、健康老龄匹配对照和成年对照(每组n = 14)。
通过定量聚合酶链反应(PCR)测定总白细胞细胞因子表达,并通过酶联免疫吸附测定(ELISA)测定肿瘤坏死因子(TNF)-α血浆浓度。通过ELISA评估内毒素(脂多糖[LPS])处理后外周血单核细胞(PBMC)的TNF-α反应。
与健康成年马相比,健康老龄马白细胞介素(IL)-6、IL-8和干扰素-γ的表达增加,LPS刺激后PBMC的TNF-α释放也增加。相比之下,患有PPID的老龄马IL-8表达增加,但其他细胞因子的表达与健康成年马相似,而非年龄匹配对照。
老龄马显示出促炎状态的证据,这可能促成与年龄相关疾病的发展。患有PPID的马IL-8表达增加,这可能影响患有PPID的马对细菌病原体的反应能力。在患有PPID的马中观察到的促炎细胞因子表达普遍下降可能是抗炎激素血浆浓度高的结果。