Department of Emergency, Etlik City Hospital, Ankara-Türkiye.
Department of Histology and Embryology, Karatay University, Konya-Türkiye.
Ulus Travma Acil Cerrahi Derg. 2024 Jul;30(7):472-479. doi: 10.14744/tjtes.2024.92575.
Traumatic liver injury is an acute event that triggers liver repair. The augmenter of liver regeneration (ALR) has been identified as a growth factor involved in this process. This study evaluates the impact of ALR on isolated liver blunt trauma and examines its relationship with various time intervals.
Forty healthy female Wistar albino rats were divided into five groups (n=8 each). Isolated blunt liver trauma was induced using a custom-designed trauma platform in all groups except for Group 1. The groups were categorized by the timing of euthanasia post-trauma: 2nd (15 minutes), 3rd (30 minutes), 4th (45 minutes), and 5th (60 minutes). Assessments included plasma ALR levels, liver tissue ALR levels (both intact and lacerated), biochemical indices, and liver histological analysis.
Plasma ALR levels in Group 4 were higher than in Groups 1 and 2 (p<0.01). Intact liver ALR levels in Groups 3 and 4 exceeded those in Group 1 (p<0.05, p<0.01, respectively). Intact liver tissue ALR levels in Group 5 were lower than in Groups 3 and 4 (p<0.05, p<0.01, respectively). Lacerated liver tissue ALR levels in Group 5 were higher than those in Groups 2 and 3. In Group 1, the plasma ALR level was higher than the intact liver tissue ALR level (p<0.05). In Group 2, plasma ALR levels exceeded those in intact liver tissue ALR levels (p<0.01). In Group 3, plasma ALR levels surpassed both lacerated and intact liver tissue ALR levels (p<0.05, p<0.001, respectively). In Group 4, the plasma ALR level was higher than the intact liver tissue ALR level (p<0.01), and the lacerated liver tissue level was higher than the intact liver ALR level (p<0.001). Additionally, inflammation scores were higher in Groups 3, 4, and 5 compared to Group 2 (p<0.05, p<0.01, p<0.01, respectively).
This study is the first to explore the role of ALR in isolated blunt liver trauma. Following blunt liver trauma, both plasma and liver tissue ALR levels change within minutes.
创伤性肝损伤是一种触发肝修复的急性事件。肝再生增强因子(ALR)已被确定为参与这一过程的生长因子之一。本研究评估了 ALR 对孤立性肝钝性创伤的影响,并研究了其与各种时间间隔的关系。
将 40 只健康雌性 Wistar 白化大鼠分为五组(每组 8 只)。除第 1 组外,所有组均使用定制的创伤平台诱导孤立性钝性肝创伤。根据创伤后安乐死的时间将组分为 2 组(15 分钟)、3 组(30 分钟)、4 组(45 分钟)和 5 组(60 分钟)。评估包括血浆 ALR 水平、肝组织 ALR 水平(完整和撕裂)、生化指标和肝组织学分析。
第 4 组的血浆 ALR 水平高于第 1 组和第 2 组(p<0.01)。第 3 组和第 4 组的完整肝 ALR 水平高于第 1 组(p<0.05,p<0.01)。第 5 组的完整肝组织 ALR 水平低于第 3 组和第 4 组(p<0.05,p<0.01)。第 5 组撕裂肝组织 ALR 水平高于第 2 组和第 3 组。在第 1 组中,血浆 ALR 水平高于完整肝组织 ALR 水平(p<0.05)。在第 2 组中,血浆 ALR 水平高于完整肝组织 ALR 水平(p<0.01)。在第 3 组中,血浆 ALR 水平均高于撕裂和完整肝组织 ALR 水平(p<0.05,p<0.001)。在第 4 组中,血浆 ALR 水平高于完整肝组织 ALR 水平(p<0.01),撕裂肝组织水平高于完整肝 ALR 水平(p<0.001)。此外,与第 2 组相比,第 3 组、第 4 组和第 5 组的炎症评分更高(p<0.05,p<0.01,p<0.01)。
本研究首次探讨了 ALR 在孤立性钝性肝创伤中的作用。钝性肝创伤后,血浆和肝组织 ALR 水平在数分钟内发生变化。