THE CEREBROSPINAL FLUID PRODUCTION IS INFLUENCED BY SYMPATHETIC NERVES IN THE CHOROID PLEXUS

Author(s):  
Maria Lindvall ◽  
Lars Edvinsson ◽  
Christer Owman
PEDIATRICS ◽  
1958 ◽  
Vol 22 (6) ◽  
pp. 1152-1152
Author(s):  
JONATHAN T. LANMAN

This Ciba Symposium records the proceedings of a meeting held in London in May, 1957 to discuss the cerebrospinal fluid. The papers presented may be roughly grouped in the fields of anatomy, physiology, and clinical medicine. Those in the field of anatomy are excellent and in keeping with the current renaissance in this field. They include observations on the early development of the telencephalic choroid plexus, suggesting a progression of diverse functions for this tissue during ontogeny, and a study of the mature choroid plexus using the electron microscope.


Science ◽  
1971 ◽  
Vol 173 (3994) ◽  
pp. 330-332 ◽  
Author(s):  
T. H. Milhorat ◽  
M. K. Hammock ◽  
J. D. Fenstermacher ◽  
D. P. Rall ◽  
V. A. Levin

Science ◽  
1978 ◽  
Vol 201 (4351) ◽  
pp. 176-178 ◽  
Author(s):  
M Lindvall ◽  
L Edvinsson ◽  
C Owman

2004 ◽  
Vol 40 (6) ◽  
pp. 277-283 ◽  
Author(s):  
P.L. Longatti ◽  
L. Basaldella ◽  
E. Orvieto ◽  
A. Fiorindi ◽  
A. Carteri

1959 ◽  
Vol 197 (4) ◽  
pp. 825-828 ◽  
Author(s):  
Edgar A. Bering

The cerebrospinal fluid production has been studied in the dog under conditions of maximum obtainable flow rates from the cisterna magna. Under these conditions the fluid had constant composition and was assumed to represent the cerebrospinal fluid in the intact state. Cerebral blood flow and cerebral oxygen consumption were measured by the method of Kety and Schmidt. The only significant correlations found were with oxygen consumption when the CSF flow rate was in terms of brain weight and with cerebral blood flow and cerebral vascular resistance when CSF flow was in terms of choroid plexus weight. A combined regression equation was calculated which satisfactorily accounted for the observed CSF flow: CSF cu mm/min. = .128 x CMRO2 x brain wgt. + 0.15 x CVR x choroid plexus wt. This suggested separate physiological processes, one correlated with oxygen metabolism and one with hydrodynamic factors of the cerebral blood flow. The data demonstrated that the choroid plexus alone could not have accounted for the entire CSF flow and some must have come from another source, presumably the brain.


Science ◽  
1969 ◽  
Vol 166 (3912) ◽  
pp. 1514-1516 ◽  
Author(s):  
T. H. Milhorat

1960 ◽  
Vol 198 (3) ◽  
pp. 665-668 ◽  
Author(s):  
Morton B. Waitzman

A specific 5-adenylic acid (5-AMP) deaminase was studied in preparations of hog ciliary process tissue. It was determined that while the activity of this deaminase is enhanced by adenosinetriphosphate (ATP), this activity is not completely blocked in the absence of ATP. Deamination proceeds only at the expense of 5-AMP, but a myokinase-like-active system may be prepared, such that 5-AMP is added to the substrate pool. In this latter case total levels of deamination are generally reflective of added 5-AMP and myokinase-like reaction accumulated 5-AMP. The general acceptance of ciliary process tissue as the site of aqueous humor production leads one to a reasonable conclusion that the very active 5-AMP deaminase studied plays some as yet unexplained role in the dynamics of aqueous secretion. Possibilities concerning the specific role(s) played are discussed. Functional analogy between aqueous humor and cerebrospinal fluid production is again suggested by the fact that an adenine nucleotide deaminase is found also in choroid plexus tissue.


1991 ◽  
Vol 71 (3) ◽  
pp. 795-800 ◽  
Author(s):  
S. Javaheri

Cerebrospinal fluid (CSF) is secreted primarily by the choroid plexus (CP) located in the cerebral ventricles. Although much is known about ionic composition of cisternal CSF, the mechanisms involved in secretion of CSF in mammals are still not understood. The main aim of this report is to critically review the role of NaCl cotransport carrier in CSF production. On the basis of the studies in the literature, a model for CSF production by the CP is proposed. In this model, CP cells are assumed to be equipped with an NaCl cotransport carrier located on the basolateral (blood-facing) membrane. Because Na+ and Cl- are the two principal ions in CSF, their continued secretions into cerebral ventricles by CP cells require an adequate intracellular supply, which may be guaranteed by the NaCl cotransport carrier. Although this appears to be a reasonable assumption, making the processes involved in CSF production similar to those of other secretory epithelial cells, the presence of such a carrier in mammalian CP remains controversial. The reasons for this controversy are critically reviewed, and some suggestions for further studies are made.


2004 ◽  
Vol 19 (1) ◽  
pp. 76-78 ◽  
Author(s):  
Kotaro Oshio ◽  
Hiroyuki Watanabe ◽  
Yaunlin Song ◽  
A. S. Verkman ◽  
Geoffrey T. Manley

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