Effect of arginine vasopressin, acetazolamide, and angiotensin II on CSF pressure at simulated altitude. 1984

L C Senay, and D L Tolbert

To test the hypothesis that arginine vasopressin (AVP) in the cerebral spinal fluid (CSF) influences CSF dynamics at simulated altitudes, cannulae were bilaterally implanted into the lateral ventricles of rabbits and rats. Recordings of CSF pressures at ambient and at various reduced barometric pressures identified an increase in CSF pressure in animals at simulated altitudes. Samples of CSF collected before and immediately after altitude exposures and assayed for AVP did not show a significant change in AVP concentration. Brain water content did not change after 6-8 h of reduced barometric pressure. Intraarterial injections of acetazolamide reduced CSF pressures, whereas intraventricular injection had no effect. Intraventricular angiotensin II (AII) elevated CSF pressures both at ambient (744-755 mm Hg) and reduced barometric pressures. When AII was preceded by saralasin, an AII blocker, the rise in CSF pressure with AII injection was prevented. Indeed, saralasin given alone, reduced or prevented the rise in CSF pressure seen at simulated altitudes. Intraventricular AVP did not influence CSF pressures nor did prostaglandins E2 and F1 alpha and norepinephrine. In AVP-deficient (Brattleboro) rats, response to intraventricular AVP depended on barometric pressure; i.e. CSF pressure rose when the rat was exposed to reduced barometric pressures and fell when the rat was exposed to ambient pressure. We suggest that hypobaric stress could cause an increase in AII content of the central nervous system which, in turn, would lead to an increase in CSF pressure. The exact mechanism of CSF pressure increase after AII increase remains to be investigated.

UI MeSH Term Description Entries
D007427 Intracranial Pressure Pressure within the cranial cavity. It is influenced by brain mass, the circulatory system, CSF dynamics, and skull rigidity. Intracerebral Pressure,Subarachnoid Pressure,Intracerebral Pressures,Intracranial Pressures,Pressure, Intracerebral,Pressure, Intracranial,Pressure, Subarachnoid,Pressures, Intracerebral,Pressures, Intracranial,Pressures, Subarachnoid,Subarachnoid Pressures
D008297 Male Males
D011817 Rabbits A burrowing plant-eating mammal with hind limbs that are longer than its fore limbs. It belongs to the family Leporidae of the order Lagomorpha, and in contrast to hares, possesses 22 instead of 24 pairs of chromosomes. Belgian Hare,New Zealand Rabbit,New Zealand Rabbits,New Zealand White Rabbit,Rabbit,Rabbit, Domestic,Chinchilla Rabbits,NZW Rabbits,New Zealand White Rabbits,Oryctolagus cuniculus,Chinchilla Rabbit,Domestic Rabbit,Domestic Rabbits,Hare, Belgian,NZW Rabbit,Rabbit, Chinchilla,Rabbit, NZW,Rabbit, New Zealand,Rabbits, Chinchilla,Rabbits, Domestic,Rabbits, NZW,Rabbits, New Zealand,Zealand Rabbit, New,Zealand Rabbits, New,cuniculus, Oryctolagus
D011910 Rats, Brattleboro A mutant strain of Rattus norvegicus used in research on renal function and hypertension and as a disease model for diabetes insipidus. Brattleboro Rats
D001921 Brain The part of CENTRAL NERVOUS SYSTEM that is contained within the skull (CRANIUM). Arising from the NEURAL TUBE, the embryonic brain is comprised of three major parts including PROSENCEPHALON (the forebrain); MESENCEPHALON (the midbrain); and RHOMBENCEPHALON (the hindbrain). The developed brain consists of CEREBRUM; CEREBELLUM; and other structures in the BRAIN STEM. Encephalon
D000086 Acetazolamide One of the CARBONIC ANHYDRASE INHIBITORS that is sometimes effective against absence seizures. It is sometimes useful also as an adjunct in the treatment of tonic-clonic, myoclonic, and atonic seizures, particularly in women whose seizures occur or are exacerbated at specific times in the menstrual cycle. However, its usefulness is transient often because of rapid development of tolerance. Its antiepileptic effect may be due to its inhibitory effect on brain carbonic anhydrase, which leads to an increased transneuronal chloride gradient, increased chloride current, and increased inhibition. (From Smith and Reynard, Textbook of Pharmacology, 1991, p337) Acetadiazol,Acetazolam,Acetazolamide Sodium, (Sterile),Acetazolamide, Monosodium Salt,Ak-Zol,Apo-Acetazolamide,Diacarb,Diamox,Diuramide,Défiltran,Edemox,Glauconox,Glaupax,Huma-Zolamide,Ak Zol,AkZol,Apo Acetazolamide,ApoAcetazolamide,Huma Zolamide,HumaZolamide
D000804 Angiotensin II An octapeptide that is a potent but labile vasoconstrictor. It is produced from angiotensin I after the removal of two amino acids at the C-terminal by ANGIOTENSIN CONVERTING ENZYME. The amino acid in position 5 varies in different species. To block VASOCONSTRICTION and HYPERTENSION effect of angiotensin II, patients are often treated with ACE INHIBITORS or with ANGIOTENSIN II TYPE 1 RECEPTOR BLOCKERS. Angiotensin II, Ile(5)-,Angiotensin II, Val(5)-,5-L-Isoleucine Angiotensin II,ANG-(1-8)Octapeptide,Angiotensin II, Isoleucine(5)-,Angiotensin II, Valine(5)-,Angiotensin-(1-8) Octapeptide,Isoleucine(5)-Angiotensin,Isoleucyl(5)-Angiotensin II,Valyl(5)-Angiotensin II,5 L Isoleucine Angiotensin II,Angiotensin II, 5-L-Isoleucine
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001127 Arginine Vasopressin The predominant form of mammalian antidiuretic hormone. It is a nonapeptide containing an ARGININE at residue 8 and two disulfide-linked cysteines at residues of 1 and 6. Arg-vasopressin is used to treat DIABETES INSIPIDUS or to improve vasomotor tone and BLOOD PRESSURE. Argipressin,Vasopressin, Arginine,Arg-Vasopressin,Argipressin Tannate,Arg Vasopressin
D001273 Atmosphere Exposure Chambers Experimental devices used in inhalation studies in which a person or animal is either partially or completely immersed in a chemically controlled atmosphere. Atmosphere Exposure Chamber,Chamber, Atmosphere Exposure,Chambers, Atmosphere Exposure,Exposure Chamber, Atmosphere,Exposure Chambers, Atmosphere

Related Publications

L C Senay, and D L Tolbert
June 2006, Clinical science (London, England : 1979),
L C Senay, and D L Tolbert
January 1987, Sports medicine (Auckland, N.Z.),
L C Senay, and D L Tolbert
January 2022, Frontiers in endocrinology,
L C Senay, and D L Tolbert
January 1984, The American journal of physiology,
L C Senay, and D L Tolbert
March 1987, Postgraduate medical journal,
L C Senay, and D L Tolbert
December 1979, The New England journal of medicine,
L C Senay, and D L Tolbert
May 2000, Journal of investigative medicine : the official publication of the American Federation for Clinical Research,
L C Senay, and D L Tolbert
September 1991, Gastroenterology,
Copied contents to your clipboard!