Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2020 Jan 19;10(1):160.
doi: 10.3390/biom10010160.

In Vitro and In Vivo Models for the Investigation of Potential Drugs Against Schizophrenia

Affiliations
Review

In Vitro and In Vivo Models for the Investigation of Potential Drugs Against Schizophrenia

Oliwia Koszła et al. Biomolecules. .

Abstract

Schizophrenia (SZ) is a complex psychiatric disorder characterized by positive, negative, and cognitive symptoms, and is not satisfactorily treated by current antipsychotics. Progress in understanding the basic pathomechanism of the disease has been hampered by the lack of appropriate models. In order to develop modern drugs against SZ, efficient methods to study them in in vitro and in vivo models of this disease are required. In this review a short presentation of current hypotheses and concepts of SZ is followed by a description of current progress in the field of SZ experimental models. A critical discussion of advantages and limitations of in vitro models and pharmacological, genetic, and neurodevelopmental in vivo models for positive, negative, and cognitive symptoms of the disease is provided. In particular, this review concerns the important issue of how cellular and animal systems can help to meet the challenges of modeling the disease, which fully manifests only in humans, as experimental studies of SZ in humans are limited. Next, it is emphasized that novel clinical candidates should be evaluated in animal models for treatment-resistant SZ. In conclusion, the plurality of available in vitro and in vivo models is a consequence of the complex nature of SZ, and there are extensive possibilities for their integration. Future development of more efficient antipsychotics reflecting the pleiotropy of symptoms in SZ requires the incorporation of various models into one uniting model of the multifactorial disorder and use of this model for the evaluation of new drugs.

Keywords: in vitro models; in vivo models; schizophrenia.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Dopaminergic and glutamatergic system abnormalities in schizophrenia (SZ). NMDA: N-methyl-D-aspartate.
Figure 2
Figure 2
SH-SY5Y cells.
Figure 3
Figure 3
Mouse hippocampal neurons (HT22) cells.

References

    1. McCutcheon R.A., Abi-Dargham A., Howes O.D. Schizophrenia, Dopamine and the Striatum: From Biology to Symptoms. Trends Neurosci. 2019;42:205–220. doi: 10.1016/j.tins.2018.12.004. - DOI - PMC - PubMed
    1. The Early Development of Kraepelin’s Ideas on Classification: A Conceptual History. PubMed—NCBI. [(accessed on 8 November 2018)]; Available online: https://www.ncbi.nlm.nih.gov/pubmed/3078049.
    1. Jackson J.H. Remarks on Evolution and Dissolution of the Nervous System. J. Ment. Sci. 1887;33:25–48. doi: 10.1192/bjp.33.141.25. - DOI
    1. Jablensky A. The diagnostic concept of schizophrenia: Its history, evolution, and future prospects. Dialogues Clin. Neurosci. 2010;12:271–287. - PMC - PubMed
    1. Ashok A.H., Baugh J., Yeragani V.K. Paul Eugen Bleuler and the origin of the term schizophrenia (SCHIZOPRENIEGRUPPE) Indian J. Psychiatry. 2012;54:95–96. - PMC - PubMed

Publication types

Substances