Isolation and perfusion of rat inner medullary vasa recta

• Published in: American journal of physiology. Renal physiology 2015-08, Vol.309 (4), p.F300-F304
• Main Authors: Evans, Kristen K, Nawata, C Michele, Pannabecker, Thomas L
• Format: Article
• Language: English
• Subjects: Animals; Biomarkers - metabolism; Blood Vessels - cytology; Blood Vessels - metabolism; Blood Vessels - physiology; Blood Vessels - ultrastructure; Capillary Permeability; Dissection - methods; Endothelium; Gene expression; Gene Expression Regulation; In Vitro Techniques; Kidney Medulla - blood supply; Loop of Henle - blood supply; Male; Microscopy, Electron; Morphology; Perfusion - methods; Rapid Report; Rats, Wistar; Renal Circulation; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - metabolism; Rodents
• ISSN: 1931-857X; 1522-1466
• DOI: 10.1152/ajprenal.00214.2015

Outer medullary isolated descending vasa recta have proven to be experimentally tractable, and consequently much has been learned about outer medullary vasa recta endothelial transport, pericyte contractile mechanisms, and tubulovascular interactions. In contrast, inner medullary vasa recta have never been isolated from any species, and therefore isolated vasa recta function has never been subjected to in vitro quantitative evaluation. As we teased out inner medullary thin limbs of Henle's loops from the Munich-Wistar rat, we found that vasa recta could be isolated using similar protocols. We isolated ∼30 inner medullary vasa recta from 23 adult male Munich-Wistar rats and prepared them for brightfield or electron microscopy, gene expression analysis by RT-PCR, or isolated tubule microperfusion. Morphological characteristics include branching and nonbranching segments exhibiting a thin endothelium, axial surface filaments radiating outward giving vessels a hairy appearance, and attached interstitial cells. Electron microscopy shows multiple cells, tight junctions, and either continuous or fenestrated endothelia. Isolated vasa recta express genes encoding the urea transporter UT-B and/or the fenestral protein PV-1, genes expressed in descending or ascending vasa recta, respectively. The transepithelial NaCl permeability (383.3 ± 60.0 × 10(-5) cm/s, mean ± SE, n = 4) was determined in isolated perfused vasa recta. Future quantitative analyses of isolated inner medullary vasa recta should provide structural and functional details important for more fully understanding fluid and solute flows through the inner medulla and their associated regulatory pathways.