Du Qiu-xiang, Sun Jun-hong, Zhang Ling-yu, Liang Xin-hua, Guo Xiang-jie, Gao Cai-rong, Wang Ying-yuan
Department of Forensic Pathology, Shanxi Medical University, 56 South Xinjian Nan Road, Taiyuan, 030001, Shanxi, People's Republic of China.
Forensic Sci Med Pathol. 2013 Dec;9(4):528-33. doi: 10.1007/s12024-013-9482-y. Epub 2013 Sep 18.
To estimate the age of skeletal muscle contusion, the expression of SNAT2 mRNA in contused skeletal muscle of rats was detected by real-time polymerase chain reaction (PCR). In total, 78 Sprague-Dawley male rats were divided into control and contusion groups. At 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, and 48 h (n = 6) after contusion, the rats were sacrificed with a lethal dose of pentobarbital. Another 24 rats received contusion injuries at 6, 12, 18, and 24 h (n = 6) after death. Total RNA was isolated from muscle specimens using the TRIzol reagent and reverse-transcribed into first-strand cDNA. Sequence-specific primers and TaqMan fluorogenic probes for SNAT2 mRNA and RPL13 mRNA were designed using the AlleleID 6 software, and the expression levels of SNAT2 mRNA were determined by real-time PCR. At 4, 16, 20, and 24 h after contusion, expression levels of SNAT2 mRNA normalized to RPL13 mRNA increased by 2.07 (P < 0.05), 2.53 (P < 0.05), 2.68 (P < 0.05), and 2.06 fold (P < 0.05) respectively, versus that in the control group. However, there was no significant change in the expression level of SNAT2 mRNA from 24 to 48 h (P > 0.05) after contusion, when normalized to RPL13 mRNA. There was no change in the expression level of SNAT2 mRNA between the normal skeletal muscle from the left limb of the same injured rat and the control. Also, no degradation of SNAT2 mRNA was detected in the postmortem samples (P > 0.05). This result suggests that the determination of SNAT2 mRNA levels by real-time PCR may be useful for estimating wound age.
为了评估骨骼肌挫伤的时间,采用实时聚合酶链反应(PCR)检测大鼠挫伤骨骼肌中SNAT2 mRNA的表达。将78只雄性Sprague-Dawley大鼠分为对照组和挫伤组。在挫伤后4、8、12、16、20、24、28、32、36、40、44和48小时(每组n = 6),用致死剂量的戊巴比妥处死大鼠。另外24只大鼠在死后6、12、18和24小时接受挫伤(每组n = 6)。使用TRIzol试剂从肌肉标本中分离总RNA,并逆转录为第一链cDNA。使用AlleleID 6软件设计针对SNAT2 mRNA和RPL13 mRNA的序列特异性引物和TaqMan荧光探针,并通过实时PCR测定SNAT2 mRNA的表达水平。与对照组相比,挫伤后4、16、20和24小时,以RPL13 mRNA标准化的SNAT2 mRNA表达水平分别增加了2.07倍(P < 0.05)、2.53倍(P < 0.05)、2.68倍(P < 0.05)和2.06倍(P < 0.05)。然而,挫伤后24至48小时,以RPL13 mRNA标准化时,SNAT2 mRNA的表达水平没有显著变化(P > 0.05)。同一受伤大鼠左肢正常骨骼肌与对照组之间,SNAT2 mRNA的表达水平没有变化。此外,在死后样本中未检测到SNAT2 mRNA的降解(P > 0.05)。该结果表明,通过实时PCR测定SNAT2 mRNA水平可能有助于评估伤口时间。