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 28;21(3):827.
doi: 10.3390/ijms21030827.

The Neuroprotective and Biomarker Potential of PACAP in Human Traumatic Brain Injury

Affiliations
Review

The Neuroprotective and Biomarker Potential of PACAP in Human Traumatic Brain Injury

Denes Toth et al. Int J Mol Sci. .

Abstract

Traumatic brain injury remains a growing public health concern and represents the greatest contributor to death and disability globally among all trauma-related injuries. There are limited clinical data regarding biomarkers in the diagnosis and outcome prediction of TBI. The lack of real effective treatment for recovery calls for research of TBI to be shifted into the area of prevention, treatment of secondary brain injury and neurorehabilitation. The neuropeptide pituitary adenylate cyclase activating polypeptide (PACAP) has been reported to act as a hormone, a neuromodulator, a neurotransmitter and a trophic factor, and has been implicated in a variety of developmental and regenerative processes. The importance of PACAP in neuronal regeneration lies in the upregulation of endogenous PACAP and its receptors and the protective effect of exogenous PACAP after different central nervous system injury. The aim of this minireview is to summarize both the therapeutic and biomarker potential of the neuropeptide PACAP, as a novel possible target molecule presently being investigated in several human conditions including TBI, and with encouraging results in animal models of TBI.

Keywords: PACAP; biomarker; neuropeptide; neuroprotective; traumatic brain injury.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Figures

Figure 1
Figure 1
The neuroprotective and biomarker potential of pituitary adenylate cyclase activating polypeptide (PACAP). Red boxes and circles indicate primary damage after traumatic brain injury (TBI), blue boxes and circles show secondary damage, while green boxes and circles indicate healthy tissue or the process (neuroprotection) leading towards regenerated tissue.

Similar articles

Cited by

References

    1. Menon D.K., Schwab K., Wright D.W., Maas A.I. Position Statement: Definition of Traumatic Brain Injury. Arch. Phys. Med. Rehabil. 2010;91:1637–1640. doi: 10.1016/j.apmr.2010.05.017. - DOI - PubMed
    1. Rusnak M. Giving voice to a silent epidemic. Nat. Rev. Neurol. 2013;9:186–187. doi: 10.1038/nrneurol.2013.38. - DOI - PubMed
    1. Rubiano A.M., Carney N., Chesnut R., Puyana J.C. Global neurotrauma research challenges and opportunities. Nature. 2015;527:S193–S197. doi: 10.1038/nature16035. - DOI - PubMed
    1. Dewan M.C., Rattani A., Gupta S., Baticulon R.E., Hung Y.-C., Punchak M., Agrawal A., Adeleye A.O., Shrime M.G., Rubiano A.M., et al. Estimating the global incidence of traumatic brain injury. J. Neurosurg. JNS. 2018;130:1080–1097. doi: 10.3171/2017.10.JNS17352. - DOI - PubMed
    1. Mondello S., Sorinola A., Czeiter E., Vámos Z., Amrein K., Synnot A., Donoghue E., Sándor J., Wang K.K.W., Diaz-Arrastia R., et al. Blood-Based Protein Biomarkers for the Management of Traumatic Brain Injuries in Adults Presenting to Emergency Departments with Mild Brain Injury: A Living Systematic Review and Meta-Analysis. J. Neurotr. 2017 doi: 10.1089/neu.2017.5182. - DOI - PMC - PubMed

MeSH terms

Substances