Zeng Delin, Basilio Andrew V, Pichay Leanne A, Ateshian Gerard A, Hansen Olivia S, Romanov Alexander, Morrison Barclay
Department of Biomedical Engineering, Columbia University, 351 Engineering Terrace MC 8904, 1210 Amsterdam Avenue, New York, NY, 10027, USA.
Department of Mechanical Engineering, Columbia University, 220 S. W. Mudd Building, 500 West 120th Street, New York, NY, 10027, USA.
Ann Biomed Eng. 2025 Apr;53(4):813-824. doi: 10.1007/s10439-024-03666-y. Epub 2024 Dec 19.
Cerebral edema is associated with poor prognosis because brain swelling within the rigid skull raises intracranial pressure, exacerbating secondary injuries following traumatic brain injury. Brain swelling can be characterized by triphasic biomechanics, which models brain tissue as a mixture of a deformable porous solid matrix with a negative fixed-charged density (FCD), water, and monovalent counterions. When brain cells die, the intracellular FCD is exposed, attracting cations into the cells. The increase in intracellular solute concentration generates osmotic pressure via the Gibbs-Donnan effect, driving water into cells and causing swelling. This study quantifies the FCD of rat and pig brain tissue by measuring the pressure generated by tissue within a confined volume as cells died. Rat brain tissue generated an averaged swelling pressure of 52.92 ± 20.40 mmHg (mean ± one standard deviation). Variations were observed between pig cortical white matter (7.14 ± 4.79 mmHg) and cortical gray matter (33.86 ± 11.89 mmHg). The corresponding FCD values were 42.54 ± 8.14 mEq/L for rat brain tissue, and 15.18 ± 5.38 mEq/L and 34.22 ± 6.31 mEq/L for pig cortical white and gray matter, respectively. Treating the rat brain tissue with DNAse, heparinase I, heparinase III, and chondroitinase ABC to degrade FCD significantly reduced swelling pressure. Good agreement between the experimental and numerically simulated responses supported the role of the FCD in cerebral edema formation. The reported FCD values can improve the biofidelity of computational models to predict post-traumatic cerebral edema, aiding the improvement of safety systems.
脑水肿与预后不良相关,因为坚硬颅骨内的脑肿胀会升高颅内压,加剧创伤性脑损伤后的继发性损伤。脑肿胀可由三相生物力学来表征,该三相生物力学将脑组织建模为具有负固定电荷密度(FCD)的可变形多孔固体基质、水和单价抗衡离子的混合物。当脑细胞死亡时,细胞内的FCD暴露出来,吸引阳离子进入细胞。细胞内溶质浓度的增加通过吉布斯-唐南效应产生渗透压,驱使水进入细胞并导致肿胀。本研究通过测量细胞死亡时受限体积内组织产生的压力来量化大鼠和猪脑组织的FCD。大鼠脑组织产生的平均肿胀压力为52.92±20.40 mmHg(平均值±一个标准差)。在猪的皮质白质(7.14±4.79 mmHg)和皮质灰质(33.86±11.89 mmHg)之间观察到了差异。大鼠脑组织相应的FCD值为42.54±8.14 mEq/L,猪皮质白质和灰质的FCD值分别为15.18±5.38 mEq/L和34.22±6.31 mEq/L。用脱氧核糖核酸酶、肝素酶I、肝素酶III和软骨素酶ABC处理大鼠脑组织以降解FCD,可显著降低肿胀压力。实验响应与数值模拟响应之间的良好一致性支持了FCD在脑水肿形成中的作用。所报道的FCD值可以提高计算模型预测创伤后脑水肿的生物逼真度,有助于改进安全系统。