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Biology of Reproduction, Vol 23, 294-304, Copyright © 1980 by Society for the Study of Reproduction
1 Department of Physiology & Biochemistry,
The University of Reading,
Whiteknights, Reading RG6 2AJ, England, U. K. The transfer of carnitine from blood into the perfused, sperm-free lumen of segments of the
epididymis has been examined in anesthetized rats. During i.v. infusion of DL-[3 H]-carnitine,
radioactive material with chromatographic properties similar to those of free carnitine appeared in
perfusates flowing at 1.0-l.3 µl/min through the distal cauda epididymidis within 30 min and
slowly attained plateau values at 2-4 h. The entry rate showed a significant (P<0.001) positive and
linear correlation with length of the perfused epididymis. Carnitine transport was independent of
the tonicity of the perfusing solution (290, 310, or 330 mOSM) and was not altered when the
following components of epididymal plasma were added individually to the perfusing solution to
produce the same final tonicity (310 mOSM): DL-carnitine (60 mM), L-carnitine (20 mM), phosphocholine (20 mM), inositol (50 mM). Perfusing solutions containing glyceropholsphocholine (20
on 40 mM) significantly increased (P<0.01; P<0.02, respectively) carnitine entry, whereas addition
of albumin (40 mg/ml) significantly reduced (P<0.01) carnitine entry. Choline (20 mM) and
betaine (20 mM), structural analogues of carnitine, both significantly augmented (P<0.001)
carnitine transfer from blood to the distal cauda to 245 and 208%, respectively, whereas glycine
and
-butyrobetaine at the same concentration were without effect. There were regional differences in the transport indices for carnitine, the rate being greatest in the mid-corpus and intermediate in the proximal cauda, exceeding that in the distal cauda epididymidis by approximately
4:2:1, respectively, at the end of the infusion. Luminal choline (20 mM) significantly increased
both the transfer of radioactivity from circulating DL-[3 H]-carnitine into the lumen of the corpus
epididymidis and the secretion of carnitine into the perfusate from
200 to 350 pmol/h/cm. In
dual isotope infusions of the enantiomers of carnitine, the transport of L-carnitine into the distal
cauda epididymidis exceeded that of the D-form 14-fold, and choline (20m mM) in the perfusing
solution stimulated the entry of both, but to different extents. A model for the transport of
carnitine across the epithelium of the epididymis is proposed.
Note:
ACKNOWLEDGMENTS
We are grateful to Dr. W.C.L. Ford and Dr. D. W.
Hamilton for helpful comments.
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