Melatonin from cerebrospinal fluid but not from blood reaches sheep cerebral tissues under physiological conditions
2014
Legros, Celine | Chesneau, Didier | Boutin, Jean A. | Leroux-Barc, Celine | Malpaux, Benoit | Physiologie de la reproduction et des comportements [Nouzilly] (PRC) ; Institut National de la Recherche Agronomique (INRA)-Institut Français du Cheval et de l'Equitation [Saumur] (IFCE)-Université de Tours (UT)-Centre National de la Recherche Scientifique (CNRS) | Biotechnologies, Pharmacie Moléculaire et Cellulaire ; Institut de Recherches Servier | Biotechnologies, Pharamcologie Moléculaire et Cellulaire ; Institut de Recherches Servier | Plateforme d'Infectiologie Expérimentale (PFIE) ; Institut National de la Recherche Agronomique (INRA) | Région Centre, INRA, IFR135
Remerciements : INRA Institut National de la Recherche Agronomique, UMR PRC Physiologie de la Reproduction et des Comportements - Plate-forme Chirurgie et Imagerie pour la Recherche et l'Enseignement, Nouzilly, France
Mostrar más [+] Menos [-]Inglés. The pineal gland secretes melatonin that circulates in the blood and cerebrospinal fluid. We provide data that support the hypothesis that, in sheep and maybe in human, only the cerebrospinal fluid melatonin, and not the blood melatonin, can provide most of melatonin to the cerebral tissue in high concentrations, particularly in the periventricular area. The melatonin content of sheep brain, our chosen animal model, was found in significant concentration gradients oriented from the ventricle (close to the cerebrospinal fluid) to the cerebral tissue, with concentrations varying by a factor of 1 to 125. The highest concentrations were observed close to the ventricle wall, whereas the lowest concentrations were furthest from the ventricles (407.0 ± 71.5 pg/ml compared to 84.7 ± 5.2 pg/ml around the third ventricle). This concentration gradient was measured in brain tissue collected at mid-day and at the end of the night. Nocturnal concentrations were higher than daytime concentrations, reflecting the diurnal variation in the pineal gland. The concentration gradient was not detected when melatonin was delivered to the brain via the bloodstream. The diffusion of melatonin to cerebral tissues via cerebrospinal fluid was supported by in vivo scintigraphy and autoradiography. 2-[(123) I]-melatonin infused into the cerebrospinal fluid quickly and efficiently diffused into the brain tissues, whereas [(123) I]-iodine (control) was mostly washed away by the cerebrospinal fluid flow and [(123) I]-BSA remained mostly in the cerebrospinal fluid. Taken together, these data support a critical role of cerebrospinal fluid in providing the brain with melatonin.
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