Salivary Gland Disease Center and Molecular Laboratory for Gene Therapy, Capital Medical University School of Stomatology, Beijing, PR China.
Int J Radiat Oncol Biol Phys. 2010 Nov 1;78(3):897-903. doi: 10.1016/j.ijrobp.2010.05.048. Epub 2010 Sep 9.
To evaluate the effect of irradiation on microvascular endothelial cells in miniature pig parotid glands.
A single 25-Gy dose of irradiation (IR) was delivered to parotid glands of 6 miniature pigs. Three other animals served as non-IR controls. Local blood flow rate in glands was measured pre- and post-IR with an ultrasonic Doppler analyzer. Samples of parotid gland tissue were taken at 4 h, 24 h, 1 week, and 2 weeks after IR for microvascular density (MVD) analysis and sphingomyelinase (SMase) assay. Histopathology and immunohistochemical staining (anti-CD31 and anti-AQP1) were used to assess morphological changes. MVD was determined by calculating the number of CD31- or AQP1-stained cells per field. A terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) apoptosis assay was used to detect apoptotic cells. The activity of acid and neutral Mg(2+)-dependent SMase (ASMase and NSMase, respectively) was also assayed.
Local parotid gland blood flow rate decreased rapidly at 4 h post-IR and remained below control levels throughout the 14-day observation period. Parotid MVD also declined from 4 to 24 hours and remained below control levels thereafter. The activity levels of ASMase and NSMase in parotid glands increased rapidly from 4 to 24 h post-IR and then declined gradually. The frequency of detecting apoptotic nuclei in the glands followed similar kinetics.
Single-dose IR led to a significant reduction of MVD and local blood flow rate, indicating marked damage to microvascular endothelial cells in miniature pig parotid glands. The significant and rapid increases of ASMase and NSMase activity levels may be important in this IR-induced damage.
评估照射对小型猪腮腺微血管内皮细胞的影响。
对 6 头小型猪的腮腺给予单次 25Gy 剂量照射(IR)。另外 3 头动物作为非照射对照。用超声多普勒分析仪在照射前后测量腺体的局部血流速率。在照射后 4 小时、24 小时、1 周和 2 周时,取腮腺组织样本进行微血管密度(MVD)分析和神经鞘磷脂酶(SMase)测定。组织病理学和免疫组织化学染色(抗-CD31 和抗-AQP1)用于评估形态学变化。通过计算 CD31 或 AQP1 染色细胞数/视野来确定 MVD。末端脱氧核苷酸转移酶 dUTP 缺口末端标记(TUNEL)凋亡检测用于检测凋亡细胞。还测定了酸性和中性 Mg(2+)-依赖性 SMase(ASMase 和 NSMase)的活性。
照射后 4 小时,局部腮腺血流速率迅速下降,在 14 天观察期间一直低于对照水平。腮腺 MVD 也从 4 小时下降到 24 小时,此后一直低于对照水平。照射后 4 至 24 小时,腮腺中 ASMase 和 NSMase 的活性水平迅速升高,然后逐渐下降。腺体中检测到凋亡核的频率也呈现类似的动力学。
单次剂量照射导致 MVD 和局部血流速率显著降低,表明小型猪腮腺微血管内皮细胞受到明显损伤。ASMase 和 NSMase 活性水平的显著快速升高可能在这种 IR 诱导的损伤中很重要。