Ko Minhee K, Yelenskiy Aleksandr, Gonzalez Jose M, Tan James C H
Doheny Eye Institute and Department of Ophthalmology, Keck School of Medicine, University of Southern California (USC), Los Angeles, CA.
University of Wisconsin, Madison, WI.
Mol Vis. 2014 Feb 7;20:163-70. eCollection 2014.
To describe live mouse, anterior chamber constant-pressure perfusion by an approach using feedback-controlled coupling of pressure and flow to maintain a preset pressure.
We established a microperfusion system that maintains a constant preset pressure in the anterior chamber of live mice by automatically regulating the microsyringe pump flow rate with a computer-controlled voltage feedback loop. Perfusion was by single-needle cannulation. We characterized the following in C57BL/6 mice aged 3-4 months in vivo: (i) pressure stability, (ii) pressure and flow rate reproducibility, (iii) total outflow facility, and (iv) anterior segment histology after perfusion.
Twenty live mice underwent perfusion. Constant pressure was quickly attained and stably maintained. The coefficient of pressure variation over time during perfusion at a preset pressure was <0.001. The average coefficient of variation for repeat pressure and flow rate measurements was 0.0005 and 0.127, respectively. The relationship between flow rate and pressure was linear for perfusions between 15 and 35 mmHg. The total outflow facility was 0.0066 µl/min/mmHg. Perfusion system resistance (0.5 mmHg/min/µl) was negligible relative to the ocular outflow resistance (147 mmHg/min/µl) at physiologically relevant perfusion pressures of 15-35 mmHg. No histological disruption of the drainage tissue was seen following perfusion.
Predetermined pressure was stably maintained during constant-pressure perfusion of live mouse eyes by a method using feedback-controlled coupling of pressure and flow along with single-needle anterior chamber cannulation. Perfusion measurements were reproducible. This approach is potentially useful for exploring aqueous drainage tissue biology, physiology, and pharmacology in live mice.
描述一种通过压力与流量反馈控制耦合的方法对活体小鼠前房进行恒压灌注,以维持预设压力。
我们建立了一种微灌注系统,通过计算机控制的电压反馈回路自动调节微量注射器泵的流速,从而在活体小鼠前房维持恒定的预设压力。灌注采用单针插管。我们在3 - 4月龄的C57BL/6小鼠体内对以下指标进行了表征:(i)压力稳定性,(ii)压力和流速的可重复性,(iii)总流出率,以及(iv)灌注后的眼前节组织学。
20只活体小鼠接受了灌注。快速达到并稳定维持了恒压。在预设压力下灌注期间,压力随时间变化的变异系数<0.001。重复压力和流速测量的平均变异系数分别为0.0005和0.127。在15至35 mmHg的灌注压力之间,流速与压力的关系呈线性。总流出率为0.0066 μl/min/mmHg。在15 - 35 mmHg的生理相关灌注压力下,灌注系统阻力(0.5 mmHg/min/μl)相对于眼流出阻力(147 mmHg/min/μl)可忽略不计。灌注后未见引流组织的组织学破坏。
通过一种利用压力与流量反馈控制耦合以及单针前房插管的方法,在活体小鼠眼的恒压灌注过程中稳定维持了预定压力。灌注测量具有可重复性。这种方法对于探索活体小鼠房水引流组织的生物学、生理学和药理学可能具有潜在用途。