Skip to main content
Log in

Increasing the activity of the neostriatum cholinergic system alters an established type of motor behavior in animals

  • Published:
Neuroscience and Behavioral Physiology Aims and scope Submit manuscript

Abstract

Chronic experiments on four dogs were performed to study the effects of bilateral, microinjection of the choline receptor agonist carbacholine and the blocking agent scopolamine into the dorsolateral part of the head of the caudate nucleus on the performance of an operant defensive reflex involving maintenance of a specified amount of flexion and on the differentiation of meaningful signals. Bilateral microinjection of carbacholine (0.1–0.4 μg in 1.5 μl of solvent) reduced the phasic component and amplified the tonic component of the operant responses, inhibited intersignal leg lifts, normalized posture, and calmed the animals, and also led to a sharp improvement in the differentiation of meaningful signals. These changes were expressed as increases of three-fold or more in the latent priod of movement initiation when the differentiation signal was used, as compared with the baseline latent period before the injections. Microinjection of the choline receptor blocker scopolamine into the striatum had the opposite effects. Unilateral microinjection of these substances produced changes mainly only on the day of dosage and had no effect on subsequent behavior, while bilateral microinjection altered the established motor behavior for a longer period of time. This affected both the motor and the sensory components of the operant response.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. O. V. Godukhin, Modulation of Synaptic Transmission in the Brain [in Russian], Nauka, Moscow (1987)

    Google Scholar 

  2. N. Dzhed, E. Gruen and Ch. D. Vudi, “The cholinergic dependence of the cortical neuronal mechanism underlying the Pavlovian winking conditioned reflex,” Fiziol. Zh. im. I. M. Sechenova,81, No. 11, 10–17 (1995).

    Google Scholar 

  3. V. P. Petropavlovskii, “Towards a method for conditioned motor reflexes.” Fiziol. Zh. SSSR,17, No. 2, 217–225 (1934).

    Google Scholar 

  4. B. F. Tolkunov, The Striatum and Sensory Specialization of the Neuronal Network [in Russian], Nauka, Leningrad (1978).

    Google Scholar 

  5. K. B. Shapovalova, “Possible neurophysiological and neurochemical mechanisms for the involvement of the striatum in controlling and initiating voluntary movement,” Fiziol. Zh. im. I. M. Sechenova,71, No. 5, 537–553 (1985).

    CAS  Google Scholar 

  6. K. B. Shapovalova, “The neostriatum and control of voluntary movement in normal conditions and pathology: facts and hypotheses,” Fiziol. Cheloveka,15, No. 3, 78–92 (1989).

    PubMed  CAS  Google Scholar 

  7. K. B. Shapovalova, “Afferent and efferent mechanisms for increasing the cholinergic activity of the striatum.” Fiziol. Zhurn. im. I. M. Sechenova,80, No. 1, 47–59 (1994).

    CAS  Google Scholar 

  8. R. L. Albin, A. B. Young, and J. B. Penney, “The functional anatomy of basal ganglia disorders,” Trends Neurosci.,12, No. 10, 366–375 (1989).

    Article  PubMed  CAS  Google Scholar 

  9. H. Bernedse and H. Groenewegen, “Organization of the thalamo-striatal projections in the rat with special emphais on the ventral striatum,” J. Comp. Neurol.,299, No. 2 187–228 (1990).

    Article  Google Scholar 

  10. A. C. Cuello, “Cholinergic components of the basal ganglia,” in: Neurotransmitters Interactions in the Basal Ganglia, M. Sandler, et al. (eds.), Raven Press, New York (1987).

    Google Scholar 

  11. Ch. Gerfen, “The neostriatal mosaic: organization in the basal ganglia,” Ann. Rev Neurosci.,15, No. 2, 285–320 (1992).

    Article  PubMed  CAS  Google Scholar 

  12. Ch. Gerfen, J. McGinty, and W. S. Young, “Dopamine differentially regulates dynorphin, Subst. P and enkephalin expression in striatal neurons: in situ hybridization histochemical analysis,” J. Neurosci.,11, No. 4, 1016–1031 (1991).

    PubMed  CAS  Google Scholar 

  13. J. C. Hong, K. Yoshikawa, T. Kanamatsu, and S. L. Sabol, “Modulation of striatal enkephalinergic neurons by antipsychotic drugs,” Fed. Proc.,44, No. 1, 2535–2539, (1985).

    PubMed  CAS  Google Scholar 

  14. H. Kita and S. T. Kitai, “Glutamate decarboxylase immunoreactive neurons in rat neostriatum. Their morphological types and population,” Brain Res.,447, No. 3, 346–352 (1988).

    Article  PubMed  CAS  Google Scholar 

  15. R. Lim, Ch. Lui, and R. Moffit, A Stereotaxic Atlas of the Dog's Brain, Springfield (1960).

  16. C. D. Marsden, and J. A. Obeso, “The functions of basal ganglia and the paradox of stereotaxic surgery in Parkinson's disease,” Brain,117, No. 4, 877–897 (1994).

    PubMed  Google Scholar 

  17. M. E. Martone, S. J. Young, D. M. Armstrong, and Ph. M. Groves, “Organization of cholinergic perikarya in the caudate nucleus in the cat,” in: Basal Ganglia, G. Bernardi, et al. (eds.), Plenum Press, New York-London (1991).

    Google Scholar 

  18. A. Parent and L. N. Hazrati, “Anatomical aspects of information processing in primate basal ganglia,” Trends Neurosci.,16, No. 3, 111–116 (1993).

    Article  PubMed  CAS  Google Scholar 

  19. P. Pasik, T. Pasik, and M. Di Figlia, “The internal organization of neostriatum in mammals,” in: The Neostriatum, I. Divac and G. Oberg (eds.), Pergamon Press, Oxford (1979).

    Google Scholar 

  20. R. Richardson and M. De Long, “A reappraisal of the functions of the nucleus basalis of Meynert,” Trends Neurosci.,11, No. 6, 264–267 (1988).

    Article  PubMed  CAS  Google Scholar 

  21. I. Scheel-Kruger, “New aspects on the functional role of acetylcholine in the basal ganglia. Interaction with other transmitters,” in: Central Cholinergic Mechanisms and Adaptive Dysfunctions, Plenum Press, New York (1985).

    Google Scholar 

  22. C. J. Wilson, H. T. Chang, and S. T. Kitai, “Firing patterns and synaptic potential of identified giant aspiny, interneurons in the rat neostriatum,” J. Neurosci.,10, No. 2, 508–519 (1990).

    PubMed  CAS  Google Scholar 

  23. C. D. Woody, T. Barfai, E. Gruen, and A. C. Nairn, “Intracellular injection of cGMP-dependent protein kinase results in increased input resistance in neurons of the mammalian motor cortex,” Brain Res.,386, No. 2, 379–385 (1986).

    Article  PubMed  CAS  Google Scholar 

  24. C. D. Woody, E. Gruen, H. Sakai, M. Sakai, and B. Swartz, “Responses of morphologically identified cortical neurons to intracellularly injected cyclic GMP,” Exper. Neurol.,91, No. 3, 580–595 (1986).

    Article  CAS  Google Scholar 

Download references

Authors

Additional information

Laboratory for the Physiology of Higher Nervous Activity, I. P. Pavlov Institute of Physiology, Russian Academy of Sciences, 6 Makarov Bank, 199034 St. Petersburg, Russia. Translated from Rossiiskii Fiziologicheskii Zhurnal imeni, I. M. Sechenova, Vol. 83, No. 1–2, pp. 35–43, January–February, 1997.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Shapovalova, K.B. Increasing the activity of the neostriatum cholinergic system alters an established type of motor behavior in animals. Neurosci Behav Physiol 28, 244–251 (1998). https://doi.org/10.1007/BF02462953

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02462953

Key words

Navigation