Australian Equine Laminitis Research Unit, School of Veterinary Science, The University of Queensland, Queensland, Australia.
Equine Vet J. 2012 Mar;44(2):230-7. doi: 10.1111/j.2042-3306.2011.00416.x. Epub 2011 Sep 5.
The pathophysiological events inhibited by prophylactic digital hypothermia that result in reduction of the severity of acute laminitis are unknown.
To determine if digital hypothermia inhibits lamellar inflammatory signalling during development of oligofructose (OF) induced laminitis.
Fourteen Standardbred horses were given 10 g/kg bwt OF by nasogastric tube with one forelimb (CRYO) continuously cooled by immersion in ice and water and one forelimb (NON-RX) at ambient temperature. Lamellae were harvested prior to the onset of lameness (24 h post OF administration, DEV group, n = 7) or at the onset of lameness (OG1 group, n = 7). Lamellar mRNA was purified and cDNA produced for real time-quantitative PCR analysis of mRNA concentrations of cytokines (IL-6, IL-1β, IL-10), chemokines (CXCL1, CXCL6, CXCL8/IL-8, MCP-1, MCP-2), cell adhesion molecules (ICAM-1, E-selectin), COX-2 and 3 housekeeping genes. Data were analysed (NON-RX vs. CRYO, NON-RX vs. archived control [CON, n = 7] lamellar tissue) using nonparametric tests.
Compared with CON, the OG1 NON-RX had increased (P<0.05) lamellar mRNA concentrations of all measured mediators except IL-10, IL-1β and MCP-1/2, whereas only CXCL8 was increased (P<0.05) in DEV NON-RX. Within the OG1 group, CRYO limbs (compared with NON-RX) had decreased (P<0.05) mRNA concentrations of the majority of measured inflammatory mediators (no change in MCP-1 and IL-10). Within the DEV group, mRNA concentrations of CXCL-1, ICAM-1, IL-1β, CXCL8 and MCP-2 were decreased (P<0.05) and the anti-inflammatory cytokine IL-10 was increased (compared with NON-RX limbs; P<0.05).
Digital hypothermia effectively blocked early lamellar inflammatory events likely to play an important role in lamellar injury including the expression of chemokines, proinflammatory cytokines, COX-2 and endothelial adhesion molecules.
This study demonstrates a potential mechanism by which hypothermia reduces the severity of acute laminitis, and may help identify molecular targets for future laminitis intervention.
目前尚不清楚预防性数字冷敷抑制急性蹄叶炎严重程度的病理生理事件的原因。
确定数字冷敷是否在寡果糖 (OF) 诱导的蹄叶炎发展过程中抑制板层炎症信号传导。
14 匹标准马通过鼻胃管给予 10 g/kg bwt OF,其中一只前肢(CRY0)通过浸入冰和水中连续冷却,另一只前肢(NON-RX)处于环境温度下。在跛行发作前(OF 给药后 24 小时,DEV 组,n = 7)或跛行发作时(OG1 组,n = 7)采集蹄叶组织。纯化板层 mRNA,并对细胞因子(IL-6、IL-1β、IL-10)、趋化因子(CXCL1、CXCL6、CXCL8/IL-8、MCP-1、MCP-2)、细胞间黏附分子(ICAM-1、E-选择素)、COX-2 和 3 管家基因的 mRNA 浓度进行实时定量 PCR 分析。使用非参数检验(NON-RX vs. CRYO,NON-RX vs. 存档对照 [CON,n = 7] 蹄叶组织)对数据进行分析。
与 CON 相比,OG1 NON-RX 中所有测量的介质的板层 mRNA 浓度均增加(P<0.05),除了 IL-10、IL-1β 和 MCP-1/2 外,而在 DEV NON-RX 中仅 CXCL8 增加(P<0.05)。在 OG1 组中,与 NON-RX 相比,CRY0 肢体(P<0.05)大多数测量的炎症介质的 mRNA 浓度降低(MCP-1 和 IL-10 无变化)。在 DEV 组中,CXCL-1、ICAM-1、IL-1β、CXCL8 和 MCP-2 的 mRNA 浓度降低(P<0.05),抗炎细胞因子 IL-10 增加(与 NON-RX 肢体相比;P<0.05)。
数字冷敷可有效阻断早期蹄叶炎症事件,这些事件可能在蹄叶损伤中发挥重要作用,包括趋化因子、前炎症细胞因子、COX-2 和内皮细胞黏附分子的表达。
本研究证明了冷敷降低急性蹄叶炎严重程度的潜在机制,并可能有助于确定未来蹄叶炎干预的分子靶标。