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1 Biology Department, Battelle,
Pacific Northwest Laboratories, Richland,
Washington
2 Department of
Gynecology and Obstetrics and the Ralph
L. Smith Human Development Research
Center, University of Kansas Medical
Center, Kansas City, Kansas
Changes in testicular vein and peripheral testosterone concentrations in mature rats were
monitored during anesthesia with six different
agents. Samples taken 2-3 minutes after initial
disturbance of the resting animal yielded mean
testicular vein testosterone levels of 59-247
ng/ml plasma in nine separate groups of rats.
Sustained anesthesia under halothane, enflurane, pentobarbital, ether, urethan, or
ketamine/promazine resulted in a decline in
testicular vein testosterone to 10-60 ng/ml by
the third hour. Luteinizing hormone levels,
measured under enflurane anesthesia, also fell
significantly by 1 and 2 hours after administration of anesthesia, although follicle-stimulating
hormone remained constant. Testes of the
enflurane-anesthetized rat were still able to respond to gonadotropins, but withdrawal of the
anesthetic did not reverse the downward trend
in testosterone. No changes in testicular blood
flow were detected during anesthesia, although
flow under urethan anesthesia was consistently slower than with other agents. The first
90 minutes of urethan anesthesia were characterized by severe fluctuations in testicular
vein testosterone. Halothane, enflurane, and
pentobarbital resulted in a larger ratio of
peripheral to testicular vein testosterone compared with ether or rapid sampling, suggesting
a reduction in turnover rate under these three
agents. Conclusions were that different
anesthetic agents can distort hormone levels
and endocrine function of the testes in various
ways, and that the production rate of testosterone by rat testes is higher than has been
previously suggested.
Key words: halothane, enflurane, ether, urethan, pentobarbital, ketamine, gonadotropins, blood flow
Submitted on December 28, 1979
Revised on April 21, 1980
Accepted on April 23, 1980
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