Literature DB >> 15549274

Kidney function in mice: thiobutabarbital versus alpha-chloralose anesthesia.

T Rieg1, K Richter, H Osswald, V Vallon.   

Abstract

Mice that lack or over-express a gene of interest are important tools for unraveling gene function. The determination of single nephron function by micropuncture or precise determination of glomerular filtration rate (GFR) by inulin clearance method require experiments under anesthesia. A good anesthetic protocol should allow for reasonable and stable glomerular and tubular function. The aim of this study was to compare the commonly used thiobutabarbital (TBB) versus alpha-chloralose (CHL) anesthesia with regard to absolute levels and the stability of blood pressure, heart rate, and kidney function. Male CD1 mice were anesthetized with TBB (100 mg/kg body weight i.p.) or CHL (120 mg/kg body weight i.p.), plus ketamine (100 mg/kg body weight i.m.) given to every mouse for analgesia. After preparation for clearance experiments, two 30-min urine collections were performed at periods 1 and 2 (P1 and P2). It was observed that heart rate and mean arterial blood pressure did not differ between TBB ( n=9) vs. CHL ( n=9) and were stable through P1 and P2. In CHL, GFR as well as fractional excretion of fluid, Na(+) and K(+) were stable from P1 to P2 (P1: 190+/-15 microl/min, 1.6+/-0.2%, 0.7+/-0.1%, 35+/-5%; percent change in P2: 1+/-6, 26+/-10, 29+/-15, 6+/-10 respectively). In TBB, GFR was significantly greater vs. CHL in P1 and did not significantly change in P2 (246+/-8 microl/min, p<0.05; percent change: -6.5+/-4). Fractional excretion of fluid, Na(+) and K(+) were not significantly different vs. CHL in P1, but significantly increased in P2 (P1: 1.5+/-0.2%, 1.1+/-0.2%, 31+/-3%; percent change in P2: 122+/-23, 128+/-21 and 29+/-6 respectively; each p<0.05 vs. P1). In conclusion, mice under both anesthetic regimens present reasonable and stable blood pressure and reasonable kidney function, but kidney reabsorption is more stable under CHL than under TBB anesthesia, which may facilitate study of the response in kidney function to acute interventions.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15549274     DOI: 10.1007/s00210-004-0982-x

Source DB:  PubMed          Journal:  Naunyn Schmiedebergs Arch Pharmacol        ISSN: 0028-1298            Impact factor:   3.000


  19 in total

Review 1.  Renal physiology of the mouse.

Authors:  P Meneton; I Ichikawa; T Inagami; J Schnermann
Journal:  Am J Physiol Renal Physiol       Date:  2000-03

2.  Some effects of pentobarbital anesthesia on renal hemodynamics, water and electrolyte excretion in the dog.

Authors:  W D BLAKE
Journal:  Am J Physiol       Date:  1957-11

3.  Chloralose/ketamine anaesthesia preserves a form of postprandial sodium chloride balance in Wistar rats.

Authors:  C J Metz; T Ise; D A Häberle
Journal:  Pflugers Arch       Date:  1996-09       Impact factor: 3.657

4.  A comparison of renal function in rats anesthetized with inactin and sodium amytal.

Authors:  M Elmer; P C Eskildsen; L O Kristensen; P P Leyssac
Journal:  Acta Physiol Scand       Date:  1972-09

5.  Inhibition of the action of antidiuretic hormone by thiobarbiturates in dogs, and on isolated frog skin.

Authors:  D A Hadfield; D J Ramsay
Journal:  J Physiol       Date:  1969-02       Impact factor: 5.182

6.  Renal concentrating ability in the uninephrectomized rat.

Authors:  E Sachtjen; L Rabinowitz; P E Binkerd
Journal:  Am J Physiol       Date:  1977-11

Review 7.  A practical guide to evaluating cardiovascular, renal, and pulmonary function in mice.

Authors:  John N Lorenz
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2002-06       Impact factor: 3.619

8.  The effect of anaesthesia and standard clearance procedures on renal function in the rat.

Authors:  S J Walter; T Zewde; D G Shirley
Journal:  Q J Exp Physiol       Date:  1989-11

9.  Effects of surgery on plasma volume and salt and water excretion in rats.

Authors:  D A Maddox; D C Price; F C Rector
Journal:  Am J Physiol       Date:  1977-12

10.  The effects of anesthesia on the excretion of an isotonic saline load in the rat.

Authors:  T F Knight; S Sansom; L Hawk; S J Frankfurt; E J Weinman
Journal:  Pflugers Arch       Date:  1978-02-22       Impact factor: 3.657

View more
  6 in total

1.  Renal phosphate wasting in the absence of adenylyl cyclase 6.

Authors:  Robert A Fenton; Fiona Murray; Jessica A Dominguez Rieg; Tong Tang; Moshe Levi; Timo Rieg
Journal:  J Am Soc Nephrol       Date:  2014-05-22       Impact factor: 10.121

2.  P2Y₂ receptor activation decreases blood pressure and increases renal Na⁺ excretion.

Authors:  Timo Rieg; Maria Gerasimova; José L Boyer; Paul A Insel; Volker Vallon
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-05-25       Impact factor: 3.619

3.  P2Y₂ receptor activation decreases blood pressure via intermediate conductance potassium channels and connexin 37.

Authors:  J A Dominguez Rieg; J M Burt; P Ruth; T Rieg
Journal:  Acta Physiol (Oxf)       Date:  2015-01-08       Impact factor: 6.311

4.  Acute inhibition of NCC does not activate distal electrogenic Na+ reabsorption or kaliuresis.

Authors:  Robert W Hunter; Eilidh Craigie; Natalie Z M Homer; John J Mullins; Matthew A Bailey
Journal:  Am J Physiol Renal Physiol       Date:  2014-01-08

5.  Quantitative renal perfusion measurements in a rat model of acute kidney injury at 3T: testing inter- and intramethodical significance of ASL and DCE-MRI.

Authors:  Fabian Zimmer; Frank G Zöllner; Simone Hoeger; Sarah Klotz; Charalambos Tsagogiorgas; Bernhard K Krämer; Lothar R Schad
Journal:  PLoS One       Date:  2013-01-07       Impact factor: 3.240

6.  Simultaneous measurement of kidney function by dynamic contrast enhanced MRI and FITC-sinistrin clearance in rats at 3 tesla: initial results.

Authors:  Frank G Zöllner; Daniel Schock-Kusch; Sandra Bäcker; Sabine Neudecker; Norbert Gretz; Lothar R Schad
Journal:  PLoS One       Date:  2013-11-18       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.