Changes in the cerebrospinal-fluid monoamines in rats with an immunoneutralization of the subcommissural organ-Reissner's fiber complex by maternal delivery of antibodies

Experimental Brain Research

Volumn 128, Issue 3, 1999, Pages 278-290

  Rodríguez, Sara ^a   Vio, Karin ^a   Wagner, Carolina ^a   Barría, Miguel ^a   Navarrete, Edison H ^a   Ramírez, Victor D ^b   Pérez Fígares, José M ^c   Rodríguez, Esteban M ^a  

^a UNIVERSIDAD AUSTRAL DE CHILE   (Chile)

^b UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

^c UNIVERSITY OF MÁLAGA   (Spain)

Author keywords

Cerebrospinal fluid; Function; Immunoneutralization; Monoamine clearance; Reissner's fiber; Subcommissural organ

Indexed keywords

GLYCOPROTEIN; LEVODOPA; MATERNAL ANTIBODY; MONOAMINE; SECRETORY PROTEIN;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN BLOOD VESSEL; CEREBROSPINAL FLUID; CONTROLLED STUDY; FEMALE; FETUS; IMMUNOMODULATION; NERVE FIBER; NONHUMAN; PLACENTAL TRANSFER; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN TRANSPORT; RAT; SUBCOMMISSURAL ORGAN;

ANIMALS; ANIMALS, NEWBORN; ANTIBODIES, ANTI-IDIOTYPIC; BIOGENIC MONOAMINES; FEMALE; FETUS; GLYCOPROTEINS; IMMUNITY, MATERNALLY-ACQUIRED; IMMUNOGLOBULIN G; LEVODOPA; MILK; PREGNANCY; RATS; RATS, SPRAGUE-DAWLEY; SUBCOMMISSURAL ORGAN;

EID: 0032819288     PISSN: 00144819     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002210050848     Document Type: Article

References (63)

1. Aguado LI, Alvial GS, Rodríguez EM (1981) Ultrastructure and immunocytochemistry of the pars distalis of the female rat when grafted under the kidney capsule and a parallel study of the plasma levels of prolactin. J Endocrinol 89:157-166
2. Alberts B, Bray D, Lewis J, Raff M, Roberts K, Watson JD (1994) Molecular biology of the cell. Garland, New York London
3. Aloe L, Levi-Montalcini R (1979) Nerve growth factor-induced transformation of immature chromaffin cells in vivo into sympathetic neurons: effect of antiserum to nerve growth factor. Proc Natl Acad Sci USA 76:1246-1250
4. Aloe L, Cozzari C, Calissano P, Levi-Montalcini R (1981) Somatic and behavioural postnatal effects of fetal injections of nerve growth factor antibodies in the rat. Nature 291:413-415
5. Chang CD, Ramírez VD (1989) Studies of the in vivo catabolism of exogenous dopamine infused through a push-pull cannula implanted in the rat caudate nucleus. Brain Res 481:265-273
6. Chi HJ, Shin SH (1978) The effect of exposure to ether on prolactin secretion and the half-life of endogenous prolactin in normal and castrated male rats. Neuroendocrinology 26:193-201
7. Davson H, Welch K, Segal MB (1987) Physiology and pathophysiology of the cerebrospinal fluid. Churchill Livingstone, Edinburgh London Melbourne New York
8. Diederen JHB, Vullings HGB, Rombout JHWM, Gunst-Schoonderwoerd ATM de (1983) The subcommissural organ-liquor fibre complex: the binding of catecholamines to the liquor fibre in frogs of the Rana esculenta complex. Acta Zool (Stockh) 64:47-5
9. Erikson JD, Eiden LE, Hoffman BJ (1992) Expression cloning of a reserpine-sensitive vesicular monoamine transporter. Proc Natl Acad Sci USA 89:10993-10997
10. Ermisch A, Sterba G, Hess J (1970) Untersuchungen zur Klärung der Funktion des Reissnerschen Fadens. In-vitro-Binding von Noradrenalin, Adrenalin und Serotonin. Experientia 26: 1319-1321
11. Espino A, Llorens J, Calopa M, Bartrons R, Rodrígues-Farré E, Ambrosio S (1995) Cerebrospinal dopamine metabolites in rats after intrastriatal administration of 6-hydroxydopamine or 1-methyl-4-phenylpyridinium ion. Brain Res 69:19-25
12. Finn JP, Edwards RH (1997) Individual residues contribute to multiple differences in ligand recognition between vesicular monoamine transporters 1 and 2. J Biol Chem 272: 16301-16307
13. Finn JP, Edwards RH (1998) Multiple residues contribute independently to differences in ligand recognition between vesicular monoamine transporters 1 and 2. J Biol Chem 273:3943-3947
14. Fromer WB, Hummel S, Unseld M, Ninnemann O (1995) Seed and vascular expression of a high-affinity transporter for cationic amino acids in Arabidopsis. Proc Natl Acad Sci USA 92: 12036-12040
15. Garrick NA, Tamarkin L, Taylor PL, Markey SP, Murphy DL (1983) Light and propranolol supress the nocturnal elevation of serotonin in the cerebrospinal fluid of rhesus monkeys. Science 221:474-476
16. Gobron S, Monnerie H, Meiniel R, Creveaux I, Lehmann W, Lamalle D, Dastugue B, Meiniel A (1996) SCO-spondin: a new member of the thrombospondin family secreted by the subcommissural organ is a candidate in the modulation of neuronal aggregation. J Cell Sci 109:1053-1061
17. Hammerl P, Hartl A, Thalhamer J (1993) Particulate nitrocellulose as a solid phase for protein immobilization in inimuno-affinity chromatography. J Immunol Methods 165:59-66
18. Hardebo JE, Owman C (1980) Characterization of the in vitro uptake of monoamines into brain microvessels. Acta Physiol Scand 108:223-229
19. Hess J, Sterba G (1972) Die Bindungsfähigkeit des Reissnerschen Fadens für Adrenalin und Noradrenalin in vivo. Acta Biol Med Germ 28:849-851
20. Hess J, Sterba G (1973) Studies concerning the function of the complex subcommissural organ-liquor fibre: the binding ability of the liquor fibre to pyrocatechin derivatives and its functional aspects. Brain Res 58:303-312
21. Hess J, Hoheisel G, Sterba G (1973) Elektronenmikroskopischer Nachweis der Bindungsfähigkeit des Reissnerschen Fadens für Noradrenalin. J Hirnforsch 14:257-260
22. Hofer H, Meiniel W, Erhardt H, Wolter A (1984) Preliminary electron-microscopical observations on the ampulla caudalis and the discharge of the material of Reissner's fibre into the capillary system of the terminal part of the tail of Ammocoetes (Agnathi). Gegenbaurs Morphol Jahrb Leipzig 130:77-110
23. Kuhananthan S, Miklasz SD, Ramírez VD (1991) Monoclonal antibodies against a dopamine-releasing protein (DARP) arrest fetal development, decrease brain catecholamines, and increase adrenal weight of neonatal rats. Mol Cell Neurosci 2: 410-417
24. Leonhardt H (1980) Ependym und circumventriculäre Organe. In: Oksche A, Vollrath L (eds) Neuroglia I. Handbuch der mikroskopischen Anatomie des Menschen, part IV, vol 10. Springer, Berlin Heidelberg New York, pp 177-665
25. Lindwall-Axelson M, Mathew C, Nilsson C, Owman C (1988) Effect of 5-hydroxytryptamine on the rate of cerebrospinal fluid production in rabbit. Exp Neurol 99:362-368
26. Liu Y, Peter D, Roghani A, Schuldiner S, Privé GG, Eisenberg D, Brecha N, Edwards RH (1992) A cDNA that suppresses MPP+ toxicity encodes a vesicular monoamine transporter. Cell 70:539-551
27. Llano DA, Ramírez VD (1994) Isolation of DARP (dopamine-releasing protein) from fetal rat brain and effects of DARP immunoneutralization on fetal mesencephalic dopamine levels. Mol Cell Neurosci 5:649-657
28. Lookingland KJ, Gunnel JW, Toney TW, Moore KE (1990) Comparison of the effects of ether and restraint stress on the activity of tuberoinfundibular dopaminergic neurons in female and male rats. Neuroendocrinology 52:99-105
29. Mantz J, Varlet C, Lecharny JB, Henzel D, Lenot P, Desmonts JM (1994) Effects of volatile anesthetics, thiopental, and ketamine on spontaneous and depolarization-evoked dopamine release from striatal synaptosomes in the rat. Anesthesiology 80: 352-363
30. Matsumoto M, Togashi H, Yoshioka M, Morii K, Hiromaki M, Tochihara M, Ikeda T, Saito Y, Saito H (1991) Significant correlation between cerebrospinal fluid and brain levels of norepinephrine, serotonin and acetylcholine in anesthetized rats. Life Sci 48:823-829
31. Meiniel R, Didier R, Molat JL, Meiniel A (1993) Developmental aspects of the subcommissural organ: and approach using lectins and monoclonal antibodies. In: Oksche A, Rodríguez EM, Fernández-Llebrez P (eds) The subcommissural organ. Springer, Berlin Heidelberg New York, pp 51-59
32. Nilsson C, Lindvall-Axelsson M, Owman C (1991) Role of the cerebrospinal fluid in volume transmission involving the choroid plexus. In: Fuxe K, Agnati E (eds) Volumen transmission in the brain. Raven, New York, pp 307-315
33. Nualart F, Rodríguez EM (1996) Immunochemical analysis of the subcommissural organ-Reissner's fiber complex using antibodies against alkylated and deglycosylated bovine Reissner's fiber glycoproteins. Cell Tissue Res 286:23-31
34. Nualart F, Hein S, Rodríguez EM, Oksche A (1991) Identification and partial characterization of the secretory glycoproteins of the bovine subcommissural organ-Reissner's fiber complex. Evidence for the existence of two precursor forms. Mol Brain Res 11:227-238
35. Nualart F, Hei S, Yulis RC, Zárraga AM, Araya A, Rodríguez E (1998) Partial sequencing of Reissner's fiber glycoprotein I (RF-Gly I). Cell Tissue Res 292:239-250
36. Oksche A (1961) Vergleichende Untersuchungen über die sekretorische Akivität des Subkommissuralorgans und den Gliacharakter seiner Zellen. Z Zellforsch Mikrosk Anat 54:549-612
37. Oksche A (1969) The subcommissural organ. J Neuro-Visc Relat [Suppl] 9:11-139
38. Olsson R (1958) Studies on the subcommissural organ. Acta Zool (Stockh) 39:71-102
39. Olsson R, Wingstrand KG (1954) Reissner's fibre and the infundibular organ in amphioxus - results obtained with Gomori's chrome alum haematoxylin. University Bergen Arbok (Publ biol stat) 14:1-14
40. Palfreyman MG, Huot S, Wagner J (1982) Value of monoamine metabolite determinations in CSF as an index of their concentrations in rat brain following various pharmacological manipulations. J Pharmacol Methods 8:183-196
41. Perlow MJ, Lake CR (1982) Daily fluctuation in catecholamines, monoamine metabolites, cyclic AMP, and gamma-aminobutyric acid. In: Wood J (ed) Neurobiology of cerebrospinal fluid, vol 1. Plenum Press, New York, pp 63-69
42. Peruzzo B, Rodríguez S, Delannoy L, Hein S, Rodríguez EM, Oksche A (1987) Ultrastructural immunocytochemical study of the massa caudalis of the subcommissural organ-Reissner's fiber complex in lamprey larvae (Geotria australis): evidence for a terminal vascular route of secretory material. Cell Tissue Res 247:367-376
43. Petrescu S, Branza-Nichita N, Nita-Lazar M, Petrescu AJ, Motas C (1995) Immunoaffinity chromatography on antibodies immobilized on nitrocellulose powder. Anal Biochem 229: 299-303
44. Reissner E (1860) Beiträge zur Kenntnis vom Bau des Rüchenmarks von Petromyzon fluviatilis L. Arch Anat Physiol 77: 545-588
45. Rodewald R, Kraehenbuhl JP (1984) Receptor-mediated transport of IgG. J Cell Biol 99:159-164
46. Rodríguez EM, Oksche A (1993) Historical landmarks in the investigation of the subcommissural organ and Reissner's fiber, In: Oksche A, Rodríguez EM, Fernández-Llebrez P (eds) The subcommissural organ. Springer, Berlin Heidelberg New York, pp 9-19
47. Rodríguez EM, Oksche A, Hein S, Rodríguez S, Yulis R (1984) Comparative immunocytochemical study of the subcommissural organ. Cell Tissue Res 237:427-441
48. Rodríguez EM, Oksche A, Hein S, Yulis CR (1992) Cell biology of the subcommissural organ. Int Rev Cytol 135:39-121
49. Rodríguez EM, Rodríguez S, Hein S (1998) The subcommissural organ. Microsc Res Tech 41:98-123
50. Rodríguez S, Rodríguez PA, Banse C, Rodríguez EM, Oksche A (1987) Reissner's fiber, massa caudalis and ampulla caudalis in the spinal cord of lamprey larvae (Geotria australis). Cell Tissue Res 247:359-366
51. Rodríguez S, Rodríguez EM, Jara P, Peruzzo B, Oksche A (1990) Single injection into the cerebrospinal fluid of antibodies against the secretory material of the subcommissural organ reversibly blocks formation of Reissner's fiber: immunocytochemical investigations in the rat. Exp Brain Res 81:113-124
52. Schöbitz K, Garrido O, Heinrichs M, Speer L, Rodríguez EM (1986) Ontogenetical development of the chick and duck subcommissural organ. Histochemistry 84:31-40
53. Schöbitz K, Rodríguez EM, Garrido O, Del Brío-León MA (1993) Ontogenetic development of the subcommissural organ with reference to the flexural organ. In: Oksche A, Rodríguez EM, Fernández-Llebrez P (eds) The subcommissural organ. Springer, Berlin Heidelberg New York, pp 41-49
54. Severs WB, Dundore RL, Baladan CD (1987) The subcommissural organ and Reissner's fiber: physiological regulation. In: Gross PM (ed) Circumventricular organs and body fluids, vol II. CRC Press, New York, pp 43-58
55. Sterba G, Ermisch A (1969) Der Reissnersche Faden als Rezeptormodell für biogene monoamine. I. Bindung von Noradrenalin und Adrenalin. Acta Biol Med Germ 22:9-14
56. Sterba G, Ermisch A, Freyer K, Hartmann G (1967) Incorporation of sulphur-35 into the subcommissural organ and Reissner's fiber. Nature 216:504
57. Sterba G, Hess J, Ermisch A (1969) Der Reissnerche Faden als Receptormodell für biogene monoamine. I. Tyrosin-Bindung an den Reissnerschen Faden von Katzen nach intraventrikulärer 3H-Tyrosin-Injektion. Pflügers Arch 310: 277-280
58. Sternberger LA, Hardy PH Jr., Cuculis JJ, Meyer HG (1970) The unlabeled antibody enzyme method of immunohistochemistry. Preparation and properties of soluble antigen-antibody complex (horseradish peroxidase-anti peroxidase) and its use in identification of spirochetes. J Histochem Cytochem 18: 315-333
59. Tijseen P (1985) Practice and theory of enzyme immunoassays. Elsevier, Amsterdam New York Oxford
60. Turner M (1996) Antibodies and their receptors. In: Roitt I, Brostoff J, Male D (eds) Immunology. Mosby, London, Baltimore Barcelona, pp 4.1-4.12
61. Van Herck H, De Boer SF, Hesp AP, Van Lith HA, Baumans V, Beynen AC (1997) Orbital bleeding in rats while under diethyl-ether anaesthesia does not influence telemetrically determined heart rate, body temperature, locomotor and eating activity when compared with anaesthesia alone. Lab Anim 31: 271-278
62. Vaughn DM, Smyth GB (1989) Different gradients for neurotransmitter metabolities and protein in horse cerebrospinal fluid. Vet Res Commun 13: 413-419
63. Wada Y, Egashira T, Takayama F, Yamanaka Y, Takada K, Takeda H, Matsumiya T (1998) Variation of monoamines and their metabolites contents in the cerebrospinal fluid of conscious rats. Jpn J Pharmacol 78:237-240