Intrastriatal dopaminergic grafts restore inhibitory control over striatal cholinergic neurons
- 26 Downloads
- 31 Citations
Summary
The aim of the study was to examine the influence of intrastriatal dopaminergic grafts on the functioning of striatal cholinergic neurons using an in vitro superfusion method. Rats bearing unilateral 6-hydroxydopamine lesion of the nigrostriatal dopaminergic system received a cell suspension obtained from ED 14 rat embryonic mesencephali which was injected into the denervated striatum. Lesioned animals displayed an ipsilateral rotation in response to amphetamine (5 mg/kg i.p.). This rotational response disappeared following grafting and there was even a significant contralateral rotation in response to the drug. Apomorphine (0.1 mg/kg s.c.) induced a contralateral rotation following the lesion. This latter response was attenuated in the grafted group. Three months after grafting 350 μm thick slices were prepared from striata from the control and experimental sides of lesioned and graft-bearing animals. The slices were preincubated either with 3H-dopamine (10-7 M) or 3H-choline (10-7 M) and then superfused with an oxygenated Krebs-Ringer solution. Stimulation with electrical pulses following preincubation with 3H-dopamine elicited a marked increase of tritium outflow from control slices. Stimulation-evoked overflow was of similar magnitude from slices from striata containing the graft, while it was much reduced in slices from lesioned striata. Amphetamine markedly potentiated the effect of electrical stimulation in slices obtained from control and graft-containing striata. Nomifensine (a dopamine uptake blocker) led to a significant decrease of the overflow of 3H-acetylcholine evoked by electrical stimulation from control striatal slices. This inhibition was antagonized by domperidone, a D2 dopamine receptor blocker, a finding which indicates that the action of nomifensine was indeed due to a potentiation of the action of endogenous dopamine released by the electrical stimulation. A similar, although somewhat attenuated, action of nomifensine and domperidone was observed for striatal slices containing the graft. Amphetamine inhibited the stimulation evoked overflow of 3H-acetylcholine in a dose-dependent manner from striatal slices obtained both from the intact and experimental sides of graft-bearing animals, while it had no action on slices from denervated striata. Finally, the dose-response curve for the inhibition of 3H-acetylcholine release by apomorphine was significantly shifted to the left for slices from the lesioned striata as compared with control slices. This leftward shift was totally abolished in the slices from the graft-containing striatum. These results indicate that the dopaminergic inhibition of the striatal cholinergic interneurons, abolished by the lesion, is restored by intrastriatal dopaminergic grafts both in vitro and in vivo. On the other hand the lack of correlation between the in vivo and the in vitro effects (rotational response vs. inhibition of 3H-acetylcholine release) suggest that the effect of such grafts on rotational behavior cannot be explained solely by their action on the striatal cholinergic neurons.
Key words
Acetylcholine release Cholinergic neurons Dopamine release Dopaminergic transplants In vitro release Neuronal transplantation Nigrostriatal systemPreview
Unable to display preview. Download preview PDF.
References
- Abrous N, Guy J, Vigny A, Calas A, Le Moal M, Herman JP (1988) Development of intracerebral dopaminergic grafts: a combined immunohistochemical and autoradiographic study of its time course and environmental influences. J Comp Neurol (in press)Google Scholar
- Agid Y, Guyenet P, Glowinski J, Beaujouan JC, Javoy F (1975) Inhibitory influence of the nigrostriatal dopamine system on the striatal cholinergic neurons in the rat. Brain Res 86: 488–492Google Scholar
- Arbilla S, Langer SZ (1980) Influence of monoamine oxidase inhibition on the release of 3H-dopamine elicited by potassium and by amphetamine from the rat substantia nigra and corpus striatum. Naunyn Schmiedeberg's Arch Pharmacol 311: 45–52Google Scholar
- Baudry M, Martres MP, Schwartz JC (1979) 3H-domperidone: a selective ligand for dopamine receptors. Naunyn Schmiedeberg's Arch Pharmacol 308: 231–237Google Scholar
- Cantrill R, Arbilla S, Zivkovic B, Langer SZ (1983) Amphetamine enhances latent dopaminergic neurotransmission in the rat striatum. Effects on 3H-acetylcholine release. Naunyn Schmiedeberg's Arch Pharmacol 322: 322–324Google Scholar
- Chéramy A, Leviel V, Glowinski J (1981) Dendritic release of dopamine in the substantia nigra. Nature 289: 537–542Google Scholar
- Choulli K, Herman JP, Rivet JM, Simon H, Le Moal M (1987) Spontaneous and graft-induced behavioral recovery after 6-OHDA lesion of the nucleus accumbens in the rat. Brain Res 407: 376–380Google Scholar
- Dunnett SB, Björklund A, Schmidt RH, Stenevi U, Iversen SD (1983a) Intracerebral grafting of neuronal cell suspensions. IV. Behavioural recovery in rats with unilateral 6-OHDA lesions following implantation of nigral cell suspensions in different forebrain sites. Acta Physiol Scand Suppl 522: 29–37Google Scholar
- Dunnett SB, Björklund A, Schmidt RH, Stenevi U, Iversen SD (1983b) Intracerebral grafting of neuronal cell suspensions. V. Behavioural recovery in rats with bilateral 6-OHDA lesions following implantation of nigral cell suspensions. Acta Physiol Scand Suppl 522: 39–47Google Scholar
- Dunnett SB, Bunch ST, Gage FH, Björklund A (1984) Dopamine-rich transplants in rats with 6-OHDA lesions of the ventral tegmental area. I. Effects on spontaneous and drug-induced locomotor activity. Behav Brain Res 13: 71–82Google Scholar
- Freund TF, Bolam JP, Björklund A, Stenevi U, Dunnett SB, Powell JF, Smith AD (1985) Efferent synaptic connections of grafted dopaminergic neurons reinnervating the host neostriatum: a tyrosine hydroxylase immunocytochemical study. J Neurosci 5: 603–616Google Scholar
- Guyenet PG, Agid Y, Javoy F, Beaujouan JC, Rossier J, Glowinski J (1975) Effects of dopaminergic receptor agonists and antagonists on the activity of neostriatal cholinergic system. Brain Res 84: 227–244Google Scholar
- Hefti F, Melamed E, Wurtman RJ (1980) Partial lesion of the dopaminergic nigrostriatal system in rat brain: biochemical characterization. Brain Res 195: 123–137CrossRefPubMedGoogle Scholar
- Herman JP, Choulli K, Le Moal M (1985a) Hyper-reactivity to amphetamine in rats with dopaminergic grafts. Exp Brain Res 60: 521–526Google Scholar
- Herman JP, Choulli K, Le Moal M (1985b) Activation of striatal dopaminergic grafts by haloperidol. Brain Res Bull 15: 543–546Google Scholar
- Herman JP, Choulli K, Geffard M, Nadaud D, Taghzouti K, Le Moal M (1986) Reinnervation of the nucleus accumbens and frontal cortex of the rat by dopaminergic grafts and effects on hoarding behavior. Brain Res 372: 210–216Google Scholar
- Herman JP, Choulli K, Abrous N, Dulluc J, Le Moal M (1988) Effects of intra-accumbens dopaminergic grafts on behavioral deficits induced by 6-OHDA lesions of the nucleus accumbens of A10 dopaminergic neurons: a comparison. Behav Brain Res 29: 73–83Google Scholar
- Hertting G, Zumstein A, Jackisch R, Hoffmann I, Starke K (1980) Modulation by endogenous dopamine of the release of acetylcholine in the caudate nucleus of the rabbit. Naunyn Schmiedeberg's Arch Pharmacol 315: 111–117Google Scholar
- Hunt P, Kennengiesser MH, Raynoaud JP (1974) Nomifensine: a new potent inhibitor of dopamine uptake into synaptosomes from rat brain corpus striatum. J Pharm Pharmacol 26: 370–371Google Scholar
- Jackisch R, Zumstein A, Hertting G, Starke K (1980) Interneurones are probably not involved in the presynaptic dopaminergic control of dopamine release in rabbit caudate nucleus. Naunyn Schmiedeberg's Arch Pharmacol 314: 129–133Google Scholar
- Jaeger CB (1985) Cytoarchitectonics of substantia nigra grafts: a light and electronmicroscopic study of immunocytochemically identified dopaminergic neurons and fibrous astrocytes. J Comp Neurol 231: 121–135Google Scholar
- Kamal LA, Arbilla S, Galzin AM, Langer SZ (1983) Amphetamine inhibits the electrically evoked release of 3H-dopamine from slices of the rabbit caudate. J Pharmacol Exp Ther 227: 446–458Google Scholar
- Kerkerian L, Bosler O, Pelletier G, Nieoullon A (1986) Striatal neuropeptide Y neurones are under the influence of the nigrostriatal dopaminergic pathway: immunohistochemical evidence. Neurosci Lett 66: 106–112Google Scholar
- Ladinsky H, Consolo S, Bianchi S, Samanin R, Ghezzi D (1975) Cholinergic-dopaminergic interaction in the striatum: the effect of 6-hydroxydopamine or pimozide treatment on the increased striatal acetylcholine levels induced by apomorphine, piribedil and D-amphetamine. Brain Res 84: 221–226Google Scholar
- Lehmann J, Langer SZ (1983) The striatal cholinergic interneuron: synaptic target of dopaminergic terminals? Neuroscience 4: 1105–1120Google Scholar
- Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193: 265–275PubMedGoogle Scholar
- McMillen B (1983) CNS stimulants: two distinct mechanisms of action for amphetamine-like drugs. Trends Pharmacol Sci 4: 429–432Google Scholar
- Nadaud D, Herman JP, Simon H, Le Moal M (1984) Functional recovery following transplantation of ventral mesencephalic cells in rats subjected to 6-OHDA lesion of the mesolimbic dopaminergic neurons. Brain Res 304: 137–141Google Scholar
- Niddam R, Arbilla S, Scatton B, Dennis T, Langer SZ (1985) Amphetamine induced release of endogenous dopamine in vitro is not reduced following pretreatment with reserpine. Naunyn Schmiedeberg's Arch Pharmacol 329: 123–127Google Scholar
- Nieoullon A, Chéramy A, Glowinski J (1977) Nigral and striatal dopamine release under sensory stimuli. Nature 269: 340–342Google Scholar
- Parker EM, Cubeddu LX (1986) Effects of d-amphetamine and dopamine synthesis inhibitors on dopamine and acetylcholine neurotransmission in the striatum. II. Release in the presence of vesicular transmitter stores. J Pharmacol Exp Ther 237: 193–203Google Scholar
- Robertson GS, Robertson HA (1987) D1 and D2 dopamine agonist synergism: separate sites of action? Trends Pharmacol Sci 8: 295–299Google Scholar
- Rose G, Gerhardt G, Strömberg I, Olson L, Hoffer B (1985) Monoamine release from dopamine-depleted rat caudate nucleus reinnervated by substantia nigra transplants: an in vivo electrochemical study. Brain Res 341: 92–100Google Scholar
- Scatton B (1982) Effect of dopamine agonists and neuroleptic agents on striatal acetylcholine transmission in the rat: evidence against dopamine receptor multiplicity. J Pharmacol Exp Ther 220: 197–202Google Scholar
- Schmidt RH, Björklund A, Stenevi U, Dunnett SB, Gage FH (1983) Intracerebral grafting of neuronal cell suspensions. III. Activity of intrastriatal cell suspension implants as assessed by measurement of dopamine synthesis and metabolism. Acta Physiol Scand Suppl 522: 19–28Google Scholar
- Seeman P (1980) Brain dopamine receptors. Pharmacol Rev 32: 229–313Google Scholar
- Starke K, Reimann W, Zumstein A, Hertting G (1978) Effect of dopamine receptor agonists and antagonists on release of dopamine in the rabbit caudate nucleus in vitro. Naunyn Schmiedeberg's Arch Pharmacol 305: 27–36Google Scholar
- Stoof JC, Thieme RE, Vrijmoed-de Vries MC, Mulder AH (1979) In vitro acetylcholine release from rat caudate nucleus as a new model for testing drugs with dopamine-receptor activity. Naunyn Schmiedeberg's Arch Pharmacol 309: 119–124Google Scholar
- Strecker RE, Sharp T, Brundin P, Zetterström T, Ungerstedt U, Björklund A (1987) Autoregulation of dopamine release and metabolism by intrastriatal nigral grafts as revealed by intracerebral dialysis. Neuroscience 22: 169–178Google Scholar
- Trabucchi M, Cheney DL, Racagni G, Costa E (1975) In vivo inhibition of striatal acetylcholine turnover by L-DOPA, apomorphine and (+)-amphetamine. Brain Res 85: 130–134Google Scholar
- Young WS, Bonner TI, Brann MR (1986) Mesencephalic dopamine neurons regulate the expression of neuropeptide mRNAs in the rat forebrain. Proc Natl Acad Sci USA 83: 9827–9831Google Scholar
- Zetterström T, Brundin P, Gage FH, Sharp T, Isacson O, Dunnett SB, Ungerstedt U, Björklund A (1986) In vivo measurement of spontaneous release and metabolism of dopamine from intrastriatal nigral grafts using intracerebral dialysis. Brain Res 362: 344–350Google Scholar
- Zigmond MJ, Acheson AL, Stachowiak MK, Stricker EM (1984) Neurochemical compensation after nigrostriatal bundle injury in an animal model of preclinical Parkinsonism. Arch Neurol 41: 856–861Google Scholar
- Zumstein A, Karduck W, Starke K (1981) Pathways of dopamine metabolism in the rabbit caudate nucleus in vitro. Naunyn Schmiedeberg's Arch Pharmacol 316: 205–217Google Scholar