PubMed Health⌕ Search

PubMed · 8951839

Velocity-dependent ankle torque in the normal rat.

Abstract

We evaluated the velocity-dependent ankle torque and associated activity of the ankle extensor muscle stretch reflexes in normal rats. A 287% increase in velocity-dependent ankle torque was observed at the highest velocity tested compared with the lowest velocity. Low velocity torques were minimally altered during general anesthesia that depressed EMG activity by up to 90%. However, velocity-dependent torque during higher velocity ankle rotations (306-612 degrees s-1 correlated with parallel increases in EMG magnitude recorded from the triceps surae muscles. General anesthesia (pentobarbital) abolished 61% of the velocity-dependent ankle torque at 612 degrees s-1. We conclude that ankle torque and ankle extensor muscle activity display velocity enhancement over a broad range. These observations indicate that protocols designed to assess ankle torque in the rat should use instrumentation to produce a broad range of velocities up to at least 600 degrees s-1.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

F J Thompson, C R Browd, P M Carvalho, J Hsiao. 1996-10-02. Velocity-dependent ankle torque in the normal rat.. https://pubmed.ncbi.nlm.nih.gov/8951839/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Stereoselective pharmacokinetics of ketamine and norketamine after racemic ketamine or S-ketamine administration during isoflurane anaesthesia in Shetland ponies.

BACKGROUND: The arterial pharmacokinetics of ketamine and norketamine enantiomers after racemic ketamine or S-ketamine i.v. administration were evaluated in seven gelding ponies in a crossover study (2-month interval). METHODS: Anaesthesia was induced with isoflurane in oxygen via a face-mask and then maintained at each pony's individual MAC. Racemic ketamine (2.2 mg kg(-1)) or S-ketamine (1.1 mg kg(-1)) was injected in the right jugular vein. Blood samples were collected from the right carotid artery before and at 1, 2, 4, 8, 16, 32, 64, and 128 min after ketamine administration. Ketamine and norketamine enantiomer plasma concentrations were determined by capillary electrophoresis. Individual R-ketamine and S-ketamine concentration vs time curves were analysed by non-linear least square regression two-compartment model analysis using PCNonlin. Plasma disposition curves for R-norketamine and S-norketamine were described by estimating AUC, C(max), and T(max). Pulse rate (PR), respiratory rate (R(f)), tidal volume (V(T)), minute volume ventilation (V(E)), end-tidal partial pressure of carbon dioxide (PE'(CO(2))), and mean arterial blood pressure (MAP) were also evaluated. RESULTS: The pharmacokinetic parameters of S- and R-ketamine administered in the racemic mixture or S-ketamine administered separately did not differ significantly. Statistically significant higher AUC and C(max) were found for S-norketamine compared with R-norketamine in the racemic group. Overall, R(f), V(E), PE'(CO(2)), and MAP were significantly higher in the racemic group, whereas PR was higher in the S-ketamine group. CONCLUSIONS: Norketamine enantiomers showed different pharmacokinetic profiles after single i.v. administration of racemic ketamine in ponies anaesthetised with isoflurane in oxygen (1 MAC). Cardiopulmonary variables require further investigation.

Anesthesia, General↗