Vol. 2 No. 3 (2019): International Journal of Aging Research
Research Articles

The Neuro Engraftment and Neuroregenerative effects of Hydrogen Sulphide Donor, Intracerebral MSCs, Ginko Biloba and Kefir in Attenuating Neuropathological hallmarks of Lipopolysaccharide induced Alzheimer’s disease Rat models

Mai M.Anwar1, Ola S.M.Ali2, Laila A. Rashed.3, Badawi A.M.1, Nadia A.Eltablawy1
1Department of Biochemistry, National Organization for Drug Control and Research (NODCAR), Giza 12511, Egypt. 2Department of Biochemistry, Faculty of Pharmacy, Al-Azhar University, cairo 11311, Egypt. 3Department of Biochemistry and Molecular Biology, Faculty of Medicine, Cairo University, Giza 12511, Egypt.


  • LPS induced rats, MSCs, hydrogen sulphide, Kefir, amyloid β, intracerebral.

How to Cite

Mai M.Anwar1, Ola S.M.Ali2, Laila A. Rashed.3, Badawi A.M.1, Nadia A.Eltablawy1. (2019). The Neuro Engraftment and Neuroregenerative effects of Hydrogen Sulphide Donor, Intracerebral MSCs, Ginko Biloba and Kefir in Attenuating Neuropathological hallmarks of Lipopolysaccharide induced Alzheimer’s disease Rat models. International Journal of Aging Research, 2(3), 38. https://doi.org/10.28933/ijoar-2019-06-2005


Background: Memory disorders have been characterized by being a devastating long term incurable diseases with a huge social impact in addition to a diminished efficient available medical treatments. Deep Brain stimulation via using neuroprotective inducers for treatment of brain structure degenerative diseases such as Alzheimer’s disease (AD) can be considered as being a promising successful therapy due to its various targets and underlying mechanisms for improving brain dysfunction. Objectives: The main aim of this study is to suggest therapeutic protocol having the potentials for restoring normal neurons diverse population and modifying neuropathological deposited hallmarks including both positive and negative lesions. Materials and Methods: Rats were divided into nine groups: (G1) control ;(G2) rats received LPS as a method of inducing nongenetically manipulated AD;(G3)AD rats received NaHS;(G4) AD rats received MSCs intracerebrally;(G5) AD rats received MSCs+NaHS;(G6)AD rats received kefir+GB;(G7)AD rats received MSCs+kefir+GB;(G8)AD rats received NaHS+kefir+GB; (G9) AD rats received MSCs+NaHS+kefir+GB. Results: AD induction resulted in down-regulation of CBS expression and GSH brain tissue level accompanied with overexpression in amyloid-? protein, MAPK, tau protein, ACAT expression and MDA brain tissue level in addition to elevated caspase-3 serum level. Conclusion: The implantation of amyloid reliving therapy that do have a wide clinical impact if initiated at benign plaques stage before irreversible brain damage occurs. The following effects have been observed following the administration of suggested medical protocol where a decrease in AD pathological deposited hallmarks has been observed with maintaining inflammatory brain factors by functioning as a potent neuroregenerative.


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