Skip to main content

Advertisement

Log in

Carvacrol suppresses learning and memory dysfunction and hippocampal damages caused by chronic cerebral hypoperfusion

  • Original Article
  • Published:
Naunyn-Schmiedeberg's Archives of Pharmacology Aims and scope Submit manuscript

Abstract

Chronic cerebral hypoperfusion (CCH) is a common phenomenon in many neurological diseases such as vascular dementia and Alzheimer’s disease. Several drugs have been investigated to prevent and treat the CCH. The carvacrol (CAR) has been shown to have beneficial effects on various neurodegenerative and neuropsychiatric disorders. Accordingly, the present study was designed to evaluate the effect of CAR on neuronal damages in hippocampus in a well-defined model for CCH. Forty-eight male Wistar rats were equally divided into four groups of sham (A), CCH (B), CCH+ CAR 25, and 50 mg/kg/daily (C and D). The animals were subjected to permanent bilateral occlusion of the carotid arteries (2-vessel occlusion, 2VO) to induce CCH model. Cognitive function was evaluated by Morris water maze test. Morphological changes of hippocampus were assessed using Nissl staining. Free radical scavenging activity was measured by 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. Moreover, catalase (CAT) and superoxide dismutase (SOD) activities and lipid peroxidation levels were measured using biochemical analysis. CAR significantly improved the spatial learning and memory deficits assessed using the Morris water maze test. CAR also significantly attenuated neuronal necrosis as well as malondialdehyde (MDA) and elevated the levels of SOD and CAT activity in the hippocampus. The results indicate that CAR produces significant neuroprotective effects on neuronal damages induced by CCH. Protective effect of CAR may be mediated by antioxidative effect of this drug.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

Download references

Acknowledgments

The information contained in this article was extracted from a master’s thesis by the author, Azadeh Shahrokhi Racini, student of medical physiology.

Funding

This work was funded by the Shahid Sadoughi University of Medical Sciences and Health Services (grant no. IR.SSU.MEDICINE.REC.1396-141)

Author information

Authors and Affiliations

Authors

Contributions

ZF, SA, and RM designed the research. SA, AF, and HZ performed these experiments. SF and RM analyzed data and ZF wrote this article and supervised the research.

Corresponding author

Correspondence to Fatemeh Zare Mehrjerdi.

Ethics declarations

All animal tests and experimental stages were approved by Ethics Committee of Yazd University of Medical Science which is in accordance with the US National Institutes of Health Publication guide for the care and use of laboratory animals. The ethics code that has been recorded in the ethics committee is IR.SSU.MEDICINE.REC.1396-141.

Conflict of interest

This article is the result of a master’s thesis by the author, Azadeh Shahrokhi Racini, student of medical physiology. She has received research grants from Shahid Sadoughi University of Medical Sciences and Health Services. The authors declare they have no conflict of interest.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Shahrokhi Raeini, A., Hafizibarjin, Z., Rezvani, M.E. et al. Carvacrol suppresses learning and memory dysfunction and hippocampal damages caused by chronic cerebral hypoperfusion. Naunyn-Schmiedeberg's Arch Pharmacol 393, 581–589 (2020). https://doi.org/10.1007/s00210-019-01754-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00210-019-01754-8

Keywords

Navigation