Differential spatiotemporal alterations in adrenoceptor mRNAs and binding sites in cerebral cortex following spreading depression: Selective and prolonged up-regulation of α(1B)-adrenoceptors

Experimental Neurology

Volumn 154, Issue 2, 1998, Pages 612-627

  Shen, Pei Juan ^a   Gundlach, Andrew L ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

Adrenergic receptors; Autoradiography; Cerebral cortex; In situ hybridization histochemistry; Receptor gene regulation; Spreading depression

Indexed keywords

ALPHA 1B ADRENERGIC RECEPTOR; ALPHA 2A ADRENERGIC RECEPTOR; BETA 1 ADRENERGIC RECEPTOR; MESSENGER RNA; NORADRENALIN; POTASSIUM CHLORIDE; RECEPTOR SUBTYPE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTORADIOGRAPHY; BRAIN CORTEX; CONTROLLED STUDY; HISTOCHEMISTRY; IN SITU HYBRIDIZATION; MALE; NEOCORTEX; NERVE CELL PLASTICITY; NEUROPROTECTION; NONHUMAN; PRIORITY JOURNAL; RAT; RECEPTOR BINDING; RECEPTOR UPREGULATION; SPREADING CORTICAL DEPRESSION;

EID: 0032438216     PISSN: 00144886     EISSN: None     Source Type: Journal    
DOI: 10.1006/exnr.1998.6915     Document Type: Article

References (91)

1. Arabia A.-M., Shen P.-J., Gundlach A. L. Ipsilateral cerebrocortical changes in CCK and NOS mRNA after induction of spreading depression in the rat. Proc. Aust. Soc. Clin. Exp. Pharmacol. Toxicol. 3:1996;84.
2. Arabia A.-M., Shen P.-J., Gundlach A. L. Increased striatal proenkephalin mRNA subsequent to production of spreading depression in rat cerebral cortex: Activation of corticostriatal pathway. Mol. Brain Res. 61:1998;195-202.
3. Arakawa S., Nakamura S., Kawashima N., Nishike S., Fujii Y. Antidromic burst activity of locus coeruleus neurons during cortical spreading depression. Neuroscience. 78:1997;1147-1158.
4. Aston-Jones G., Chiang C., Alexinsky T. Discharge of noradrenergic locus coeruleus neurons in behaving rats and monkeys suggests a role in vigilance. Prog. Brain Res. 88:1991;501-520.
5. Audet M. A., Doucet G., Oleskevich S., Descarries L. Quantified regional and laminar distribution of the noradrenaline innervation in the anterior half of the adult rat cerebral cortex. J. Comp. Neurol. 274:1988;307-318.
6. 2. Neuropharmacology. 35:1996;679-687.
7. Bing G., Filer D., Miller J. C., Stone E. A. Noradrenergic activation of immediate early genes in rat cerebral cortex. Mol. Brain Res. 11:1991;43-46.
8. 1b1a. J. Neurochem. 57:1991;1548-1555.
9. Boyeson M. G., Feeney D. M. Intraventricular norepinephrine facilitates motor recovery following sensorimotor cortex injury. Pharmacol. Biochem. Behav. 35:1990;497-501.
10. Boyeson M. G., Krobert K. A. Cerebellar norepinephrine infusions facilitate recovery after sensorimotor cortex injury. Brain Res. Bull. 29:1992;435-439.
11. 2. Nucleic Acids Res. 18:1990;682.
12. Caggiano A. O., Breder C. D., Kraig R. P. Long-term elevation of cyclooxygenase-2, but not lipoxygenase, in regions synaptically distant from spreading depression. J. Comp. Neurol. 376:1996;447-462.
13. 1. Endocrinology. 133:1993;2263-2268.
14. 2. Proc. Natl. Acad. Sci. USA. 86:1989;4853-4857.
15. Dagerlind Å., Friberg K., Bean A. J., Hökfelt T. Sensitive mRNA detection using unfixed tissue: Combined radioactive and non-radioactive in situ hybridization histochemistry. Histochemistry. 98:1992;39-49.
16. 1a1b1d. J. Chem. Neuroanat. 13:1997;115-139.
17. Dietrich W. D., Feng Z. C., Leistra H., Watson B. D., Rosenthal M. Photothrombotic infarction triggers multiple episodes of cortical spreading depression in distant brain regions. J. Cereb. Blood Flow Metab. 14:1994;20-28.
18. Dunn-Meynell A., Pan S., Levin B. E. Focal traumatic brain injury causes widespread reductions in rat brain norepinephrine turnover from 6 to 24 h. Brain Res. 660:1994;88-95.
19. 1. Synapse. 19:1995;88-96.
20. Feeney D. M., Westerberg V. S. Norepinephrine and brain damage: α Noradrenergic pharmacology alters functional recovery after cortical trauma. Can. J. Psychol. 44:1990;233-252.
21. Ferry B., Magistretti P. J., Pralong E. Noradrenaline modulates glutamate-mediated neurotransmission in the rat basolateral amygdala in vitro. Eur. J. Neurosci. 9:1997;1356-1364.
22. 2B. Proc. Natl. Acad. Sci. USA. 88:1991;1019-1023.
23. Follesa P., Mocchetti I. Regulation of basic fibroblast growth factor and nerve growth factor mRNA by β-adrenergic receptor activation and adrenal steroids in rat central nervous system. Mol. Pharmacol. 43:1992;132-138.
24. 1B. J. Biol. Chem. 270:1995;5614-5619.
25. Gross R. A., Ferrendelli J. A. Relationships between norepinephrine and cyclic nucleotides in brain and seizure activity. Neuropharmacology. 21:1982;655-661.
26. 3. Brain Res. 672:1995;214-227.
27. 2. J. Cereb. Blood Flow Metab. 10:1990;885-894.
28. Hadcock J. R., Malbon C. C. Agonist regulation of gene expression of adrenergic receptors and G proteins. J. Neurochem. 60:1993;1-9.
29. +. Acta Physiol. Scand. 109:1980;1-6.
30. Harley C. Noradrenergic and locus coeruleus modulation of the perforant path-evoked potential in rat dentate gyrus supports a role for the locus coeruleus in attentional and memorial processes. Prog. Brain Res. 88:1991;307-321.
31. 12. Naunyn Schmiedeberg's Arch. Pharmacol. 354:1996;404-410.
32. 2. Mol. Neuropharmacol. 1:1992;219-229.
33. Inoue M., McHugh M., Pappius H. M. The effect of α-adrenergic receptor blockers prazosin and yohimbine on cerebral metabolism and biogenic amine content of traumatized brain. J. Cereb. Blood Flow Metab. 11:1991;242-252.
34. Jacobs O., Van Bree L., Mailleux P., Zhang F., Schiffmann S. N., Halleux P., Albala N., Vanderhaeghen J. J. Homolateral cerebrocortical increase of immediate early gene and neurotransmitter messenger RNAs after minimal cortical lesion: Blockade byND. Neuroscience. 59:1994;827-836.
35. Kamisaki Y., Hamahashi T., Hamada T., Maeda K., Itoh T. Presynaptic inhibition by clonidine of neurotransmitter amino acid release in various brain regions. Eur. J. Pharmacol. 217:1992;57-63.
36. 1b. J. Neuroendocrinol. 8:1996;449-455.
37. Kasamatsu T. Adrenergic regulation of visuocortical plasticity: A role of the locus coeruleus system. Prog. Brain Res. 88:1991;599-616.
38. Kobayashi S., Harris V. A., Welsh F. A. Spreading depression induces tolerance of cortical neurons to ischemia in rat brain. J. Cereb. Blood Flow Metab. 15:1995;721-727.
39. Kokaia Z., Gido G., Ringstedt T., Bengzon J., Kokaia M., Siesjo B. K., Persson H., Lindvall O. Rapid increase of BDNF mRNA levels in cortical neurons following spreading depression: Regulation by glutamatergic mechanisms independent of seizure activity. Mol. Brain. Res. 19:1993;277-286.
40. Kraig R. P., Dong L. M., Thisted R., Jaeger C. B. Spreading depression increases immunohistochemical staining of glial fibrillary acidic protein. J. Neurosci. 11:1991;2187-2198.
41. Kuhar M. J., Unnerstall J. R. Receptor autoradiography. Methods in Neurotransmitter Receptor Analysis. 1990;Raven, New York. p. 177-218.
42. 2. J. Biol. Chem. 266:1991;10470-10478.
43. Lauritzen M., Rice M. E., Okada Y., Nicholson C. Quisqualate, kainate and NMDA can initiate spreading depression in the turtle cerebellum. Brain Res. 475:1988;317-327.
44. 1c1A. Mol. Pharmacol. 46:1994;414-422.
45. Leão A. A. P. Spreading depression of activity in the cerebral cortex. J. Neurophysiol. 7:1944;359-390.
46. Levin B. E., Pan S., Dunn-Meynell A. Chronic alterations in rat brain α-adrenoceptors following traumatic brain injury. Restor. Neurol. Neurosci. 7:1994;5-12.
47. Lew R., Summers R. J. Autoradiographic localization of β-adrenoceptor subtypes in guinea-pig kidney. Br. J. Pharmacol. 85:1985;341-348.
48. 1A. J. Biol. Chem. 266:1991;6365-6369.
49. 1. J. Biol. Chem. 265:1990;12960-12965.
50. 2. J. Neurosci. 15:1995;152-164.
51. Marrannes R., Willems R., De Prins E., Wauquier A. Evidence for a role of theND. Brain Res. 457:1988;226-240.
52. Mason S. T., Corcoran M. E. Depletion of brain noradrenaline, but not dopamine, by intracerebral 6-hydroxydopamine potentiates convulsions induced by electroshock. J. Pharm. Pharmacol. 31:1979;209-211.
53. Matsushima K., Hakim A. M. Transient forebrain ischemia protects against subsequent focal cerebral ischemia without changing cerebral perfusion. Stroke. 26:1995;1047-1052.
54. Matsushima K., Hogan M. J., Hakim A. M. Cortical spreading depression protects against subsequent focal cerebral ischemia in rats. J. Cereb. Blood Flow Metab. 16:1996;221-226.
55. McCune S. K., Voigt M. M., Hill J. M. Expression of multiple α adrenergic receptor subtype messenger RNAs in the adult rat brain. Neuroscience. 57:1993;143-151.
56. 33. Mol. Pharmacol. 29:1986;321-330.
57. Nedergaard M., Hansen A. J. Spreading depression is not associated with neuronal injury in the normal brain. Brain Res. 449:1988;395-398.
58. Nicholas A. P., Hökfelt T., Pieribone V. A. The distribution and significance of CNS adrenoceptors examined with in situ hybridization. Trends Pharmacol. Sci. 17:1996;245-255.
59. 12. Neuroscience. 56:1993;1023-1039.
60. Obrenovitch T. P., Zilkha E. Inhibition of cortical spreading depression by L-701,324, a novel antagonist at the glycine site of theND. Br. J. Pharmacol. 117:1996;931-937.
61. Olenik C., Lais A., Meyer D. K. Effects of unilateral cortex lesions on gene expression of rat cortical cholecystokinin neurons. Mol. Brain. Res. 10:1991;259-265.
62. Oleskevich S., Descarries L., Lacaille J. C. Quantified distribution of the noradrenaline innervation in the hippocampus of adult rat. J. Neurosci. 9:1989;3803-3815.
63. O'Shea R. D., Gundlach A. L. Regulation of cholecystokinin receptors in the hypothalamus of the rat: Reciprocal changes in magnocellular nuclei induced by food deprivation and dehydration. J. Neuroendocrinol. 5:1993;697-704.
64. O'Shea R. D., Gundlach A. L. Quantitative analysis of in situ hybridization histochemistry. Wisden W., Morris B. J. In Situ Hybridization Protocols for the Brain. 1994;57-78 Academic Press, London.
65. Pavlasek J., Haburcak M., Masanova C., Orlicky J. Increase of catecholamine content in the extracellular space of the rat's brain cortex during spreading depression wave as determined by voltammetry. Brain Res. 628:1993;145-148.
66. Paxinos G., Watson C. The Rat Brain in Stereotaxic Coordinates. 1986;Academic Press, Sydney.
67. 1B. J. Neurosci. 12:1992;3869-3876.
68. 1. J. Neurosci. 14:1994;4252-4268.
69. 1. J. Neurotrauma. 9:1992;269-279.
70. 12. Proc. Natl. Acad. Sci. USA. 81:1984;1585-1589.
71. 2A. J. Neurochem. 68:1997;47-57.
72. 1. Eur. J. Pharmacol. 300:1996;9-16.
73. Robinson J. P., Kendall D. A. Inositol phospholipid hydrolysis and potentiation of cyclic AMP formation by noradrenaline in rat cerebral cortex slices are not mediated by the same α-adrenoceptor subtypes. J. Neurochem. 52:1989;690-698.
74. Seguela P., Watkins K. C., Geffard M., Descarries L. Noradrenaline axon terminals in adult rat neocortex: An immunocytochemical analysis in serial thin sections. Neuroscience. 35:1990;249-264.
75. Shen P.-J., Arabia A.-M., Gundlach A. L. Differential effects of adrenoceptor blockade on cortical immediate early gene mRNAs following cerebral infarction. Soc. Neurosci. Abstr. 22:1996;1768.
76. 1b. Proc. Aust. Neurosci. Soc. 8:1997;96.
77. 12. Mol. Brain. Res. 28:1995;222-230.
78. Shen P.-J., Gundlach A. L. Differential increases in chromogranins, but not synapsin I, in cortical neurons following spreading depression: Implications for functional roles and transmitter peptide release. Eur. J. Neurosci. 10:1998;2217-2230.
79. Shinohara M., Dollinger B., Brown G., Rapoport S., Sokoloff L. Cerebral glucose utilization: Local changes during and after recovery from spreading cortical depression. Science. 203:1979;188-190.
80. Sibley D. R., Lefkowitz R. J. Molecular mechanisms of receptor desensitization using the β-adrenergic receptor-coupled adenylate cyclase system as a model. Nature. 317:1985;124-129.
81. Steindler D. A. Locus coeruleus neurons have axons that branch to the forebrain and cerebellum. Brain Res. 223:1981;367-373.
82. Storozhuk V. M., Sachenko V. V., Kruchenko J. A. Dependence of sensorimotor cortex neuron activity on noradrenergic and serotoninergic transmission in unspecific thalamic nuclei. Neuroscience. 68:1995;315-322.
83. Sutin J., Shao Y. Resting and reactive astrocytes express adrenergic receptors in the adult rat brain. Brain Res. Bull. 29:1992;277-284.
84. Sutton R. L., Feeney D. M. α-Noradrenergic agonists and antagonists affect recovery and maintenance of beam-walking ability after sensorimotor cortex ablation in the rat. Restor. Neurol. Neurosci. 4:1992;1-11.
85. Ungerstedt U. Stereotaxic mapping of the monoamine pathways in the rat brain. Acta Physiol. Scand. 367:1971;1-48.
86. Unnerstall J. R., Fernandez I., Orensanz L. M. The α-adrenergic receptor: Radiohistochemical analysis of functional characteristics and biochemical differences. Pharmacol. Biochem. Behav. 22:1985;859-874.
87. 1B. Nucleic Acids Res. 18:1990;1053.
88. 1B. Neuroscience. 76:1997;901-913.
89. 22A. Neuroscience. 76:1997;241-260.
90. 3. Neuroscience. 76:1997;261-272.
91. Wisden W., Morris B. J. In situ hybridization with synthetic oligonucleotide probes. Wisden W., Morris B. J. In Situ Hybridization Protocols for the Brain. 1994;9-34 Academic Press, London.