Key result
Sham intravenous dosing in male Cynomolgus monkeys caused a small transient increase in cTnI concentration (~5-25 pg/mL) compared to low resting values (mean 2.5 pg/mL).
Why the study?
Does restraint for oral or intravenous dosing affect serum cTnI concentrations in male cynomolgus monkeys?
Observational
Does restraint for oral or intravenous dosing affect serum cTnI concentrations in male cynomolgus monkeys?
Restraint for intravenous dosing in cynomolgus monkeys can cause small, transient increases in cardiac troponin I, which is important for differentiating handling effects from drug toxicity in preclinical studies.
Handling during IV dosing may artifactually raise cTnI in cynomolgus monkeys; extends need to control for restraint effects in preclinical cardiac biomarker studies.
BACKGROUND: There is a paucity of information regarding cardiac troponin (cTn) concentrations in peripheral blood of nonhuman primates (NHP). Even less is known regarding cTn concentrations in monkeys that are restrained for oral or intravenous (iv) dosing. OBJECTIVES: The objectives of these studies were to (1) determine cardiac troponin I (cTnI) concentration in resting Cynomolgus monkeys and investigate biologic variability in cTnI concentration over time, (2) determine cTnI changes in restrained monkeys given sham oral dosing, and (3) determine cTnI changes in restrained NHP given a sham intravenous dosing. METHODS: The Research Use Only Erenna cTnI ultrasensitive immunoassay based on single molecule counting technology was used to determine serum cTnI concentration in longitudinal studies of male Cynomolgus monkeys at rest, and after sham oral and intravenous dosing. Animals were catheterized prestudy, and blood samples were collected by an automated sampling device to limit disturbance of the animals during studies. RESULTS: In resting monkeys cTnI concentrations were relatively low and constant and ranged from 0.2 to 9.6 pg/mL (mean = 2.5 pg/mL), with minimal variability during a 24-hour period. Animals given sham oral dosing also had low cTnI concentration with little variability similar to the resting values. Several animals restrained for intravenous dosing had a small transient increase in cTnI concentration (~5-25 pg/mL) that resolved quickly within one to 3 hours postinjection. CONCLUSIONS: Results of this longitudinal study provide information that may be important in differentiating effects of animal handling from those associated with compound-related effects in preclinical toxicology studies of drugs in development.
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Schultze et al. (2015) reported an observational. Sham oral and intravenous dosing vs. Resting state was evaluated on cardiac troponin I (cTnI) concentration. Sham intravenous dosing in male Cynomolgus monkeys caused a small transient increase in cTnI concentration (~5-25 pg/mL) compared to low resting values (mean 2.5 pg/mL).
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