References
- Armstead, W. M. 1999. Nociceptin/orphanin FQ dilates pial arteries by KATP and Kca channel activation. Brain Res 835, 315-323. https://doi.org/10.1016/S0006-8993(99)01623-6
- Berger, R. and Garnier, Y. 2000. Perinatal brain injury. J Perinat Med 28, 261-285.
- Black, S. M., Bedolli, M. A., Martinez, S., Bristow, J. D., Ferriero, D. M. and Soifer, S. J. 1995. Expression of nitric oxide synthase corresponds to regions of selective vulnerability to hypoxia-ischaemia in the developing rat brain. Neurobiol Dis 2, 145-155. https://doi.org/10.1006/nbdi.1995.0016
-
Boado, R. J. and Pardridge, W. M. 1994. Differential expression of
${\alpha}$ -actin mRNA and immunoreactive protein in brain microvascular pericytes and smooth muscle cells. J Neurosci Res 39, 430-435. https://doi.org/10.1002/jnr.490390410 - Bode, H. and Bubl, R. 1991. Brain circulation in residual cerebral damage. A Doppler ultrasound study. Monatsschr Kinderheilkd 139, 144-510.
- Cavazzuti, M. and Duffy, T. E. 1982. Regulation of local cerebral blood flow in normal and hypoxic newborn dogs. Ann Neurol 11, 247-257. https://doi.org/10.1002/ana.410110304
- Clarren, S. K., Alvord, E. C. Jr., Sumi, S. M., Streissguth, A. P. and Smith, D. W. 1978. Brain malformations related to prenatal exposure to ethanol. J Pediatr 92, 64-67. https://doi.org/10.1016/S0022-3476(78)80072-9
-
Connor, M., Yeo, A. and Henderson, G. 1996. The effect of nociceptin on
$Ca^{2+}$ channel current and intracellular$Ca^{2+}$ in the SH-SY5Y human neuroblastoma cell line. Br J Pharmacol 118, 205-207. https://doi.org/10.1111/j.1476-5381.1996.tb15387.x - Dammann, O. and Leviton, A. 1997. The role of perinatal brain damage in developmental disabilities: An epidemiologic perspective. Ment Retard Dev Disabil Res Rev 3, 13-21. https://doi.org/10.1002/(SICI)1098-2779(1997)3:1<13::AID-MRDD3>3.0.CO;2-Y
- Dobbing, J. and Sands, J. 1979. Comparative aspects of the brain growth spurt. Early Hum Dev 3, 79-83. https://doi.org/10.1016/0378-3782(79)90022-7
- Faber, E. S., Chambers, J. P., Evans, R. H. and Henderson, G. 1996. Depression of glutamatergic transmission by nociceptin in the neonatal rat hemisected spinal cord preparation in vitro. Br J Pharmacol 119, 189-190. https://doi.org/10.1111/j.1476-5381.1996.tb15969.x
- Ferriero, D. M., Holtzman, D. M., Black, S. M. and Sheldon, R. A. 1996. Neonatal mice lacking neuronal nitric oxide synthase are less vulnerable to hypoxic-ischemic injury. Neurobiol Dis 3, 64-71. https://doi.org/10.1006/nbdi.1996.0006
- Fukuda, K., Kato, S., Mori, K., Nishi, M., Takeshima, H., Iwabe, N., Miyata, T., Houtani, T. and Sugimoto, T. 1994. cDNA cloning and regional distribution of a novel member of the opioid receptor family. FEBS Lett 343, 42-46. https://doi.org/10.1016/0014-5793(94)80603-9
- Fukuda, S., Kato, T., Kuwabara, S., Kato, I., Futamura, M. and Togari, H. 2005. The ratio of flow velocities in the middle cerebral and internal carotid arteries for the prediction of cerebral palsy in term neonates. J Ultrasound Med 24, 149-153.
- Gleason, C. A., Iida, H., Hotchkiss, K. J., Northington, F. J. and Traystman, R. J. 1997. Newborn cerebrovascular responses after first trimester moderate maternal ethanol exposure in sheep. Pediatr Res 42, 39-45. https://doi.org/10.1203/00006450-199707000-00007
- Goodlett, C. R. and West, J. R. 1992. Fetal Alcohol Effects: Rat model of alcohol exposure during the brain growth spurt, pp. 45-75. In: Zagon, I. S. and Slotkin, T. A. (eds.), Maternal substance abuse and the developing nervous system. Academic Press: San Diego, USA.
- Goodlett, C. R., Marcussen, B. L. and West, J. R. 1990. A single day of alcohol exposure during the brain growth spurt induces brain weight restriction and cerebellar Purkinje cell loss. Alcohol 7, 107-114. https://doi.org/10.1016/0741-8329(90)90070-S
- Greisen, G. 1992. Effect of cerebral blood flow and cerebrovascular autoregulation on the distribution, type and extent of cerebral injury. Brain Pathol 2, 223-228. https://doi.org/10.1111/j.1750-3639.1992.tb00695.x
- Grether, J. K., Cummins, S. K. and Nelson, K. B. 1992. The California cerebral palsy project. Paediatr Perinat Epidemiol 6, 339-351. https://doi.org/10.1111/j.1365-3016.1992.tb00774.x
- Griffiths, M. J., Messent, M., MacAllister, R. J. and Evans, T. W. 1993. Aminoguanidine selectively inhibits inducible nitric oxide synthase. Br J Pharmacol 110, 963-968. https://doi.org/10.1111/j.1476-5381.1993.tb13907.x
- Gu, H., Hu, D., Hong, X. R., Li, W., Cui, Y., Hui, N. and Sha, J. Y. 2003. Changes of hypothalamus and peripheral orphanin in fetal rats with intrauterine ischemia and hypoxia. Zhonghua Fu Chan Ke Za Zhi 38, 683-684.
- Guo, Y., Ward, M. E., Beasjours, S., Mori, M. and Hussain, S. N. 1997. Regulation of cerebellar nitric oxide production in response to prolonged in vivo hypoxia. J Neurosci Res 49, 89-97. https://doi.org/10.1002/(SICI)1097-4547(19970701)49:1<89::AID-JNR10>3.0.CO;2-#
- Henderson, G. and McKnight, A. T. 1997. The orphan opioid receptor and its endogenous ligand - nociceptin/orphanin FQ. Trends Pharmacol Sci 18, 293-300.
- Higuchi, Y., Hattori, H., Hattori, R. and Furushom K. 1996. Increased neurons containing neuronal nitric oxide synthase in the brain of a hypoxic-ischemic neonatal rat model. Brain Dev 18, 369-375. https://doi.org/10.1016/0387-7604(96)00019-8
- Hou, M., Uddman, R., Tajti, J. and Edvinsson, L. 2003. Nociceptin immunoreactivity and receptor mRNA in the human trigeminal ganglion. Brain Res 964, 179-186. https://doi.org/10.1016/S0006-8993(02)03927-6
-
Hu, J. and Van Eldik, L. J. 1996.
$S100{\beta}$ induces apoptotic cell death in cultured astrocytes via a nitric oxide-dependent pathway. Biochim Biophysics Acta 1313, 239-245. https://doi.org/10.1016/0167-4889(96)00095-X - Huttenlocher, P. R., de Courten, C., Garey, L. J. and Van der Loos, H. 1982. Synaptogenesis in human visual cortex- evidence for synapse elimination during normal development. Neurosci Lett 33, 247-252. https://doi.org/10.1016/0304-3940(82)90379-2
- Ikonomidou, C., Bittigau, P., Ishimaru, M. J., Wozniak, D. F., Koch, C., Genz, K., Price, M. T., Stefovska, V., Horster, F., Tenkova, T., Dikranian, K. and Olney, J. W. 2000. Ethanol-induced apoptotic neurodegeneration and fetal alcohol syndrome. Science 287, 1056-1060. https://doi.org/10.1126/science.287.5455.1056
- Jones, K. L. and Smith, D. W. 1973. Recognition of the fetal alcohol syndrome in early infancy. Lancet 2, 999-1001.
- Kimura, K. A., Parr, A. M. and Brien, J. F. 1996. Effect of chronic maternal ethanol administration on nitric oxide synthase activity in the hippocampus of the mature fetal guinea pig. Alcohol Clin Exp Res 20, 948-953. https://doi.org/10.1111/j.1530-0277.1996.tb05276.x
- Kruse, J. 1984. Alcohol use during pregnancy. Am Fam Physician 29, 199-203.
- Lachowicz, J. E., Shen, Y., Monsma, F. J. Jr. and Sibley, D. R. 1995. Molecular cloning of a novel G protein-coupled receptor related to the opiate receptor family. J Neurochem 64, 34-40.
- Lassen, N. A. 1964. Autoregulation of cerebral blood flow. Circ Res 14/15(Suppl 1), 201-204.
- Leech, R. W. and Alvord, E. C. Jr. 1977. Anoxic-ischemic encephalopathy in the human neonatal period. The significance of brain stem involvement. Arch Neurol 34, 109-113. https://doi.org/10.1001/archneur.1977.00500140063013
- Lou, H. C. 1988. The "lost autoregulation hypothesis" and brain lesions in the newborn - an update. Brain Dev 10, 143-146. https://doi.org/10.1016/S0387-7604(88)80016-0
- Meunier, J. C. 1997. Nociceptin/orphanin FQ and the opioid receptor-like ORL1 receptor. Eur J Pharmacol 340, 1-15. https://doi.org/10.1016/S0014-2999(97)01411-8
- Meunier, J. C., Mollereau, C., Toll, L., Suaudeau, C., Moisand, C., Alvinerie, P., Butour, J. L., Guillemot, J. C., Ferrara, P., Monsarrat, B., Mazarguil, H., Vassart, G., Parmentier, M. and Costentin, J. 1995. Isolation and structure of the endogenous agonist of opioid receptor-like ORL1 receptor. Nature 377, 532-535. https://doi.org/10.1038/377532a0
- Meyrick, B. and Reid, L. 1978. The effect of continued hypoxia on rat pulmonary arterial circulation. An ultrastructural study. Lab Invest 38, 188-200.
- Miller, M. W. 1988. Effect of prenatal exposure to ethanol on the development of cerebral cortex: I. Neuronal generation. Alcohol Clin Exp Res 12, 440-444. https://doi.org/10.1111/j.1530-0277.1988.tb00223.x
- Mollereau, C., Simons, M. J., Soularue, P., Liners, F., Vassart, G., Meunier, J. C. and Parmentier, M. 1996. Structure, tissue distribution, and chromosomal localization of the prepronociceptin gene. Proc Natl Acad Sci USA 93, 8666-8670. https://doi.org/10.1073/pnas.93.16.8666
- Molliver, M. E., Kostovic, I. and van der Loos, H. 1973. The development of synapses in cerebral cortex of the human fetus. Brain Res 50, 403-407. https://doi.org/10.1016/0006-8993(73)90741-5
-
Morikawa, H., Fukuda, K., Mima, H., Shoda, T., Kato, S. and Mori, K. 1998. Nociceptin receptor-mediated
$Ca^{2+}$ channel inhibition and its desensitization in NG108-15 cells. Eur J Pharmacol 351, 247-252. https://doi.org/10.1016/S0014-2999(98)00306-9 - Nehls, V. and Drenckhahn, D. 1993. The versatility of microvascular pericytes: from mesenchyme to smooth muscle? Histochemistry 99, 1-12. https://doi.org/10.1007/BF00268014
- Nelson, R. M., Calo, G., Guerrini, R., Hainsworth, A. H., Green, A. R. and Lambert, D. G. 2000. Nociceptin/orphanin FQ inhibits ischaemia-induced glutamate efflux from rat cerebrocortical slices. Neuroreport 11, 3689-3692. https://doi.org/10.1097/00001756-200011270-00020
-
Nicol, B., Lambert, D. G., Rowbotham, D. J., Smart, D. and McKnight, A. T. 1996. Nociceptin induced inhibition of
$K^+$ evoked glutamate release from rat cerebrocortical slices. Br J Pharmacol 119, 1081-1083. https://doi.org/10.1111/j.1476-5381.1996.tb16007.x - Pantazis, N. J., West, J. R. and Dai, D. 1998. The nitric oxide-cyclic GMP pathway plays an essential role in both promoting cell survival of cerebellar granule cells in culture and protecting the cells against ethanol neurotoxicity. J Neurochem 70, 1826-1838.
- Phillips, D. E., Cummings, J. D. and Wall, K. A. 2000. Prenatal alcohol exposure decreases the number of nitric oxide synthase positive neurons in rat superior colliculus and periaqueductal gray. Alcohol 22, 75-84. https://doi.org/10.1016/S0741-8329(00)00108-7
- Rice. J. E. 3rd, Vannucci, R. C. and Brierley, J. B. 1981. The influence of immaturity on hypoxic-ischemic brain damage in the rat. Ann Neurol 9, 131-141. https://doi.org/10.1002/ana.410090206
- Richardson, B. S., Patrick, J. E., Bousquet, J., Homan, J. and Brien, J. F. Cerebral metabolism in fetal lamb after maternal infusion of ethanol. Am J Physiol 249, R505-R509.
- Roland, E. H. and Hill, A. 1997. How important is perinatal asphyxia in the causation of brain injury? Ment Retard Dev Disabil Res Rev 3, 22-27. https://doi.org/10.1002/(SICI)1098-2779(1997)3:1<22::AID-MRDD4>3.0.CO;2-Z
- Silva, M. T., Rose, S., Hindmarsh, J. G., Aislaitner, G., Gorrod, J. W., Moore, P. K., Jenner, P. and Marsden, C. D. 1995. Increased striatal dopamine efflux in vivo following inhibition of cerebral nitric oxide synthase by the novel monosodium salt of 7-nitro indazole. Br J Pharmacol 114, 257-258. https://doi.org/10.1111/j.1476-5381.1995.tb13219.x
- Taudorf, K. and Vorstrup, S. 1989. Cerebral blood flow abnormalities in cerebral palsied children with a normal CT scan. Neuropediatrics 20, 33-40. https://doi.org/10.1055/s-2008-1071262
- Volpe, J. J., Herscovitch, P., Perlman, J. M., Kreusser, K. L. and Raichle, M. E. 1985. Positron emission tomography in the asphyxiated term newborn: parasagittal impairment of cerebral blood flow. Ann Neurol 17, 287-296. https://doi.org/10.1002/ana.410170312
- Wadhwa, P. D., Sandman, C. A. and Garite, T. J. 2001. The neurobiology of stress in human pregnancy: implications for prematurity and development of the fetal central nervous system. Prog Brain Res 133, 131-142. https://doi.org/10.1016/S0079-6123(01)33010-8
- West, J. R., Chen, W. J. and Pantazis, N. J. 1994. Fetal alcohol syndrome: the vulnerability of the developing brain and possible mechanisms of damage. Metab Brain Dis 9, 291-322. https://doi.org/10.1007/BF02098878
- West, J. R., Hamre, K. M. and Cassell, M. D. 1986. Effects of ethanol exposure during the third trimester equivalent on neuron number in rat hippocampus and dentate gyrus. Alcohol Clin Exp Res 10, 190-197. https://doi.org/10.1111/j.1530-0277.1986.tb05070.x
- Yamada, K., Tsuzura, S. and Matsuda, H. 1995. Brain MRI and single photon emission computed tomography in severe athetotic cerebral palsy: a comparative study with mental and motor disorders. No To Hattatsu 27, 269-275.
- Yamamoto, S., Nishizawa, S., Tsukada, H., Kakiuchi, T., Yokoyama, T., Ryu, H. and Uemura, K. 1998. Cerebral blood flow autoregulation following subarachnoid hemorrhage in rats: chronic vasospasm shifts the upper and lower limits of the autoregulatory range toward higher blood pressures. Brain Res 782, 194-201. https://doi.org/10.1016/S0006-8993(97)01278-X
- Yu, T. P. and Xie, C. W. 1998. Orphanin FQ/nociceptin inhibits synaptic transmission and long-term potentiation in rat dentate gyrus through postsynaptic mechanisms. J Neurophysiol 80, 1277-1284.
- Zou, J. Y., Martinez, D. B., Neafsey, E. J. and Collins, M. A. 1996. Binge ethanol-induced brain damage in rats: effect of inhibitors of nitric oxide synthase. Alcohol Clin Exp Res 20, 1406-1411. https://doi.org/10.1111/j.1530-0277.1996.tb01141.x