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Graft function was monitored for 7 hours after transplantation.
Differentiated osteoblastic function was monitored by measuring alkaline phosphatase activity.
Neuromuscular function was monitored using a TOF-Watch SX (MSD, Tokyo, Japan).
The infusions continued for 6 h, during which renal function was monitored.
Differentiated BMSCs function was monitored by measuring alkaline phosphates activity of the cells.
Bone marrow function was monitored during treatment in terms of Hb, WBC and PLT counts in blood every other week.
For an estimation of potential kidney toxicity, the renal function was monitored with quantitative 99mTc-DMSA scintigraphy.
Renal function was monitored by the determination of 99mTc-DMSA uptake in the kidneys and by measuring blood urea nitrogen and creatinine levels in the plasma.
Each session was preceded and followed by a 20 minute period during which cardiovascular function was monitored in the operant chambers, but drug was not available.
Cardiovascular function was monitored continuously using a Finometer device and saliva was collected for the assessment of 3-methoxy-phenylglycol (MHPG, the major metabolite of norephinephrine).
Rocuronium 0.3 or 0.6 mg/kg (G03 and G06) was administered intravenously (IV) and neuromuscular function was monitored with an acceleromyograph.
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