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Department of Biomedical Sciences, Ontario Veterinary College, University of Guelph, Guelph, Ontario N1G 2W1 Canada
Address all correspondence and requests for reprints to: Dr. Alastair J. S. Summerlee, Office of the Dean of Graduate Studies, University Centre, University of Guelph, Guelph N1G 2W1, Ontario, Canada. E-mail: alastair{at}exec.admin.uoguelph.ca
Experiments were done to examine whether rat relaxin is dipsogenic and
whether such dipsogenic effects of rat relaxin are related to time of
injection during the light-dark cycle. Female rats were fitted with a
chronic intra-cerebro-ventricular (icv) cannula. Rat relaxin (2.5, 5,
10, 25, 50, or 100 ng/2 µl in 0.9% saline) was injected into the
right lateral ventricle at either morning (08001000 h), afternoon
(14001600 h), or night (22002400 h), and water consumption was
measured. Relaxin caused a dose-dependent dipsogenesis at doses
5 ng, but the sensitivity and magnitude of the response varied with the
photoperiod. Water consumption was smallest (3.5 ± 0.7 ml at 50
ng) and least sensitive (minimal effective dose at 25 ng) in the
afternoon and maximal (17.7 ± 2.3 ml at 50 ng) and most sensitive
(minimal effective dose 5 ng) at night. The latency from injection to
drinking was 55.8 ± 10.4 sec (mean ± SEM) and
did not vary significantly with either the dose or time of day.
A second set of experiments was done to examine the effects of neutralizing the central actions of relaxin on drinking behavior in pregnancy. Pregnant rats were injected daily, through a chronically implanted icv cannula, with either a specific monoclonal antibody raised against rat relaxin from day 12 to day 22 of gestation or with saline as a control. Drinking and eating behavior and weight gain were monitored every 12 h during pregnancy. There was a significant decrease in water consumed at night, but no effect on drinking during the day in relaxin-neutralized rats. These animals also showed a decrease in weight gain during pregnancy compared with controls and gave birth to lighter-weight litters.
These data provide evidence that the dipsogenic response to exogenous rat relaxin in female rats varies with time of injection during the light-dark cycle and suggest that relaxin in the brain may have a role in nighttime drinking behavior during the second half of pregnancy.
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