SummaryA technique for chronic cannulation of the muscular branch of the femoral vein in the rat is described. The method was validated by the application of vascular corrosion casts and comparative analysis of lactate concentration with mixed venous blood and arterial samples taken through the cannulas during lower hindlimb muscle contraction in anaesthetized rats.
Keywords: Skeletal muscle; Corrosion cast; Lactate, Arterio-venous difference; Blood samplingThe comparison of arterial and venous blood samples from thigh muscles could be useful for the study of biochemical and metabolic muscle responses to exercise in rats during experiments involving the lower hindlimb, since this allows the determination of several parameters of arterio-venous differences that undergo alterations during exercise, such as oxygen consumption, gas exchange rate, pH, lactate, ammonium and others.A technique is described for obtaining representative sequential blood samples from thigh muscle areas. A cannula was inserted through the muscular branch tributary of the femoral vein. Implantation of the cannula does not block circulation and allows withdrawal of venous blood from skeletal muscles of the lower hindlimb. Moreover, simultaneous cannulation of the aorta and right heart (which has been Correspondence to: T Pages. 1992; accepted 19 October 1992 considered as representative of mixed venous blood) allows the comparison of blood composition at 3 locations in order to study the arterio-venous difference during training exercise before and after mixing of lower hindlimb muscular venous blood with cephalic and splanchnic circulatory return.
Received 3 JulyTo verify the origin of blood withdrawn from the femoral vein by means of this technique, a vascular corrosion cast method was used to provide the complete arterio-venous tributary tree from the cannulated vessel. A report of changes in regional lactate blood concentration during lower hindlimb exerciseinduced by electric stimulation is also given.
Material and methods
AnimalsWistar adult male rats weighing 250-300 g were used. Animals were housed in propylene cages (Technoplast, Italy) at 21 ± O·5°C, 700/0humidity and 12 h L-D cycle, and fed laboratory chow (Panlab A4, Spain) and tap water ad libitum.