Single nephron glomerular filtration rate measured by linescan multiphoton microscopy compared to conventional micropuncture

被引:10
|
作者
Costanzo, Vincenzo [1 ,2 ]
D'Apolito, Luciano [2 ,3 ]
Sardella, Donato [4 ]
Iervolino, Anna [2 ]
La Manna, Gaetano [1 ]
Capasso, Giovambattista [2 ]
Frische, Sebastian [4 ]
Trepiccione, Francesco [2 ,3 ]
机构
[1] Univ Bologna, Dept Expt Diagnost & Specialty Med, Bologna, Italy
[2] Biogem, Inst Mol Biol & Genet, Ariano Irpino, Italy
[3] Univ Campania Luigi Vanvitelli, Dept Med Translat Sci, Via Pansini 5, I-80131 Naples, Italy
[4] Aarhus Univ, Dept Biomed, Aarhus, Denmark
来源
关键词
Micropuncture; Single nephron glomerular filtration rate; Linescan; Multiphoton microscopy; Kidney physiology; Ischemia/reperfusion; KIDNEY; ULTRAFILTRATION; HYPERFILTRATION; RECEPTORS; DOPAMINE; INCREASE; INJURY; MODEL;
D O I
10.1007/s00424-022-02686-8
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Renal micropuncture, which requires the direct access to the renal tubules, has for long time been the technique of choice to measure the single nephron glomerular filtration rate (SNGFR) in animal models. This approach is challenging by virtue of complex animal preparation and numerous technically difficult steps. The introduction of intravital multiphoton microscopy (MPM) offers another approach to the measure of the SNGFR by mean of the high laser-tissue penetration and the optical sectioning capacity. Previous MPM studies measuring SNGFR in vivo relied on fast full-frame acquisition during the filtration process obtainable with high performance resonant scanners. In this study, we describe an innovative linescan-based MPM method. The new method can discriminate SNGFR variations both in conditions of low and high glomerular filtration, and shows results comparable to conventional micropuncture both for rats and mice. Moreover, this novel approach has improved spatial and time resolution and is faster than previous methods, thus enabling the investigation of SNGFR from more tubules and improving options for data-analysis.
引用
收藏
页码:733 / 741
页数:9
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