Dr. John O. OLANLOKUN

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 OLANLOKUN

Name:  Oludele J. Olanlokun

Designation: Senior Lecturer
Faculty: Basic Medical Sciences
Department: Biochemistry
Phone Number:08038014201

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Biography:

Dr John Oludele Olanlokun obtained his B.Sc degree in Biochemistry from Ondo State University, Ado-Ekiti in 1998. He bagged his M.Sc in Biochemistry from University of Ibadan in 2003 and also his Ph.D. from University of Ibadan in 2014. Shortly after his first degree, he joined the services of Ondo State University, Ado-Ekiti (now Ekiti State University) in 2002 as a Graduate Assistant in the Department of Biochemistry and rose to become a lecturer I in the Department. He served the University meritoriously until 2012. In 2012, he joined the services of University of Ibadan and rose to become a Senior Lecturer in October 2018. His area of specialization is Membrane Biochemistry and Biotechnology and has delved into drug discovery and development for the treatment and prevention of malaria and mitochondrial dysfunction. He has unequivocally, purified and characterized some natural products with therapeutic potentials in the treatment of resistant malaria in mouse model. Currently, he is working on mitochondrial dynamics in Plasmodium infection and chemotherapy. He has published his research findings in peer reviewed journals.

Research

Current Research and Capacity Building Projects including Grants

Title: Mitochondrial dynamics by resistant Plasmodium berghei infection and the role of modiaquine chemotherapy in mice
Funder:
Mitochondrial dynamics is crucial in the regulation of cell homeostasis especially in infectious disease state such as malaria. Malaria is one of the most widespread infectious disease in the tropics with high fatality due to the resistance of the infectious parasites to drugs. The clinical symptoms begins when the merozoite is clinically diagnosed in the blood and include fever and organ failure. Metabolic signs of Plasmodium infection includes bioenergetics stress and altered energy metabolism in the host mitochondria. Mitochondria are dynamic organelles whose outer and inner membranes continuously undergo fusion and fission events due to the activities of some of their proteins.. These fusion and fission are mediated by distinct proteins such as Mitofusin 1, Mitofusin 2 and Optic Atrophy 1. Mitofusin 1 recruits dynamin-related protein 1 (DRP-1) and it forms a multiple subunit band around the mitochondria, leading to fission. Mfn1/2 connects inner and outer mitochondria membranes while OPA 1 fuses the inner membrane. Both fusion and fission brings about mitochondrial biogenesis and mitophagy which balances biogenesis. Transcription Factor A mitochondria (Tfam) plays a role in maintaining the mitochondrial DNA (mtDNA) copy number and transcription. PGC-1α increase mitochondrial respiration and energetic capacity for ATP synthesis. The PINK-Parkin pathway is the most well described mechanism for mitophagy. Information provided in this study will describe the short and long-term suitability of some orthodox drugs in malaria chemotherapy.
Role: Principal Investigator
Collaborators:
1. Neil Anthony Koorbanally
School of Chemistry and Physics, University of Kwazulu-Natal, Durban 4000, South Africa.
2. Geinhard Prinsloo
Department of Agriculture and Animal Health, University of South Africa, Florida Campus, Florida, 1710, South Africa
3. Paul Steenkamp
Research Centre for Plant Metabolomics, Department of Biochemistry, University of Johannesburg, Johannesburg, 2006, South Africa

Completed Research

Mefloquine and curcumin combinations blunt Aquaporin-3, MAPK, FIKK12, modulate glycolytic processes and mitochondrial respiration in Plasmodium berghei-infected mice

Malaria parasites have complex mitochondrial metabolism connected to oxidative phosphorylation. Therefore, the high metabolic demand turns glycolysis into an essential energy generating process. These parasites are aerobic glycolytic organisms with a modified TCA mainly fueled by glutamine and glutamate and low OXPHOS. In essence, survival of parasites in the host will depend largely on the regulation of host glycolysis. Mefloquine is an established drug for malaria treatment. The effects of mefloquine on the expression of FIKK, aquaporin-3, MAPK proteins and oxidative phosphorylation via the expression of some electron transport proteins and the modulatory roles of curcumin in these processes have not been reported. We hypothesized therefore, that mefloquine’s multiple molecular mechanistic role as an antiplasmodial agent involves serine/threonine kinase inhibition and aquaporin-3 gene silencing. This study will provide information on the role of curcumin on host mitochondrial respiration, glycolysis, signaling through the MAPK pathway, and antioxidant status in both susceptible and resistant malaria using Plasmodium bergheias the causative agent.

 

Publications

 

SELECTED PUBLICATIONS

 1. Olanlokun, J.O., David, O.M. and Afolayan, J.A. (2017).In vitroantiplasmodial activity and prophylactic potentials of extract and fractions of Tremaorientalis (Linn.) stem bark. BMC Complementary and Alternative Medicine. Vol. 17:407-418. (United Kingdom) (Contribution: 70%).

2. Olanlokun, J.O.,Olotu, A.F., David, O.M., Idowu, T.O., Soliman, E.S.M. and Olorunsogo, O.O. (2018). A novel compound purified from Alstoniaboonei inhibits Plasmodium falciparum Lactate dehydrogenase and Plasmepsin II. Journal of Biomolecular Structure and Dynamics. Vol. 37, NO. 8: 2193–2200 (United Kingdom) (Contribution: 50%).

3. Olanlokun, J.O.,Balogun, F. A., Olorunsogo, O.O. (2018). Chemotherapeutic and prophylactic antimalarial drugs induce cell death through mitochondrial-mediated apoptosis in murine models. Drug and Chemical Toxicology Vol 44, No 1: 47-57 (United Kingdom) (Contribution: 70%).
 
4. Adeoye, A.O., Olanlokun, J.O., Tijani, H., Lawal, S.O., Babarinde, C.O., Akinwole, M.T., Bewaji, C.O. (2019). Molecular docking analysis of apigenin and quercetin from ethylacetate fraction of Adansoniadigitata with malaria-associated calcium transport protein: An in silico approach. Heliyon Vol 5, No: e02248 (Netherlands) (Contribution: 30%).

5. Olanlokun, J.O., Balogun AA, OLorunsogo OO (2020). Regulated rutin co-administration reverses mitochondrial-mediated apoptosis in Plasmodium berghei-infected mice. Biochemical Biophysical Research Communication Vol 522 No 2: 328-334. (Netherlands) (Contribution: 70%)

6. Olanlokun J.O., Lawal O.S. Olorunsogo O.O. (2020) Modulatory Effects of Ethyl Acetate and Methanol Fractions of the Stem Bark Extract of Alstoniaboonei on Mitochondrial-Mediated Apoptosis. Journal of Herbs, Spices and Medicinal Plants Vol 26, No 4: 1-16. (United States of America ) (Contribution: 70%)

7. Olanlokun J.O., Olotu F.A., Idowu O.T., Agoni C., David O.M., Soliman M, Olorunsogo O.O. (2020). In vitro, in silico studies of newly isolated tetrahydro-4-(7-hydroxy-10- methoxy-6, 14-dimethyl-15-m-tolylpentadec-13-enyl) pyran-2-one and isobutyryl acetate compounds from Alstoniaboonei stem bark. Journal of Molecular Structure Vol 1216: 128225-128240. (Netherlands) (Contribution: 50%)

8. Olanlokun, J.O., Babarinde, C.O., Olorunsogo, O.O. (2020). Antimalarial properties and preventive effects on mitochondrial dysfunction by extract and fractions of Phyllanthusamarus (Schum. And Thonn) in Plasmodium berghei-infected mice. Journal of Basic and Clinical Physiology and Pharmacology. Vol 32 No 3:255-266. (Germany) (Contribution: 70%).

9. Olanlokun JO, Bodede O., Prinsloo G., Olorunsogo OO. (2021). Comparative antimalarial, toxicity and mito-protective effects of Diospyrosmespiliformis Hochst. ex A. DC. and Mondiawhitei (Hook.f.) Skeels on Plasmodium berghei infection in mice. Journal of Ethnopharmacology. Vol 268: 113585. (Ireland) (Contribution: 60%)

10. David OM, Olanlokun, JO, Owoniyi BE, Ayeni M, Ebenezer O, Koorbanally N. (2021). Studies on the mitochondrial, immunological and inflammatory effects of solvent fractions of DiospyrosmespiliformisHochst in Plasmodium berghei infected mice. Scientific Reports. Vol 11: 6941. (United Kingdom) (Contribution: 60%).

11. Olanlokun, JO, Okoro PO, Lawal OS, Bodede O, Olotu FA, Idowu TO, Prinsloo G, Soliman ME, Olorunsogo OO (2021). Betulinic acid purified from Alstoniaboonei inhibits folate biosynthesis in malarial Plasmodium, enhances mitochondrial pore opening and F1F0 ATPase in mice. Journal of Molecular Structure. Vol 1239:130454. (Netherlands) (Contribution: 50%).

12. Olanlokun, JO, Olowofolahan AO, Bodede O, Adegbuyi AT, Prinsloo G, Steenkamp P, Olorunsogo OO (2021). Anti-inflammatory potentials of the n-hexane fraction of Alstoniaboonei stem bark in lipopolysaccharide-induced inflammation in Wistar rats. Journal of Inflammation Research Vol 14: 3905-3920 (New Zealand). (Contribution: 60%).

13. Olanlokun JO,Okoro PO, Olorunsogo OO (2021). The roles of betulinic acid on circulating concentrations of creatine kinase and immunomodulation in mice infected with chloroquine-susceptible and resistant strains of Plasmodium berghei. Journal of Parasitic Diseases (India) (Contribution: 70%)

14. Olanlokun JO, Balogun AA, Olorunsogo OO (2021). Influence of artesunate combinative therapy co-administration with rutin on inflammatory cytokines and immunoglobulins in plasmodium berghei-infected mice. The Journal of Parasitology Vol 107, No 4: 639-647 (United States of America) (Contribution: 70%)

15. Olanlokun JO, Ekundayo MT, Ebenezer O, Koorbanally NA, Olorunsogo OO (2021). Antimalarial and erythrocyte membrane stability properties of Globimetulabraunii leaves (Engle van Tiegh) growing on cocoa in Plasmodium berghei-infected mice. Journal of Infection and Drug Resistance. Vol 14, 3795-3808 (New Zealand) (Contribution: 60%)

16. Bello IJ, Oyebode OT, Olanlokun JO, Omodara TO, Olorunsogo OO (2021). Plumbagin induces testicular damage via mitochondrial-dependent cell death. Chemico-Biological Interactions. Vol 347: 109582. (Ireland) (Contribution: 30%).

17. Olanlokun JO, Olorunsogo OO (2021) Azadirachtaindica (A. Juss.) and Curcuma longa (L.) modulate immunoglobulin and cytokine levels in Plasmodium berghei-infected mice. Journal of Comparative Clinical Pathology. 30: 871-880 (United Kingdom) (Contribution: 80%).

18. Oyebode OT, Olanlokun JO, Salami O, Obi I,Bodede O, Prinsloo G, Olorunsogo OO (2021) Terpene-rich fractions of Ficusmucoso (Welw) modulate lipopolysaccharide-induced inflammatory mediators and aberrant permeability of the inner mitochondrial membrane in murine animal model. InflammopharmacologyDoi: 10.1007/s10787-021-00876-x. (Switzerland) (Contribution: 40%).

19. Olanlokun JO, Abiodun WO, Ebenezer O, Koorbanally NA, Olorunsogo OO (2021). Curcumin modulates multiple cell death responses, matrix metalloproteinase activation and cardiac protein release in susceptible and resistant Plasmodium berghei-infected mice. Biomedicine and Pharmacotherapy. Vol. 146: 112454 (France) (Contribution: 70%)

20. Olanlokun JO, Ekundayo MT, Koorbanally NA, Olorunsogo OO (2022). Hexane fraction of Globimetulabraunii induces mitochondria-mediated apoptosis in Plasmodium berghei-induced mice. Toxicology Reports. Vol. 9: 769-777 (Ireland) (Contribution: 60%)

Supervision

SUPERVISION OF STUDENTS (Selected)

CURRENT STUDENTS

MastersLevel: Four students

Doctoral Level: Two students

Fellowship Level: Nil

 

PREVIOUS STUDENTS (Selected)

MastersLevel

Student’s name: BALOGUN, FolashadeAbimbola
Project title: Chemotherapeutic and prophylactic antimalarial drugs induce cell death through mitochondrial-mediated apoptosis in murine models.
Examining Body: Post-graduate School, University of Ibadan.
Year of Completion: 2018.

Student’s name: BALOGUN, AbayomiAdisa
Project title: Regulated rutin co-administration reverses mitochondrial-mediated apoptosis in Plasmodium berghei-infected mice.
Examining Body: Post-graduate School, University of Ibadan.
Year of Completion: 2019.

Student’s name: EKUNDAYO, Mercy Toluwase
Project title: Antimalarial and erythrocyte membrane stability properties of Globimetulabraunii leaves (Engle van Tiegh) growing on cocoa in Plasmodium berghei-infected mice.
Examining Body: Post-graduate School, University of Ibadan.
Year of Completion: 2019.

Student’s name: OKORO Praise Oghenegare
Project title: Betulinic acid purified from Alstoniaboonei inhibits folate biosynthesis in malarial Plasmodium, enhances mitochondrial pore opening and F1F0 ATPase in mice
Examining Body: Post-graduate School, University of Ibadan.
Year of Completion: 2021.

Student’s name: ABIODUN, Wisdom Oshireku
Project title: Curcumin modulates multiple cell death responses, matrix metalloproteinase activation and cardiac protein release in susceptible and resistant Plasmodium berghei-infected mice. Examining Body: Post-graduate School, University of Ibadan.
Year of Completion: 2021.

Doctoral level

Student’s name: BABARINDE, CECILIA Opeyemi
Project title: Molecular mechanism of antiplasmodial actions of natural products purified from Phyllanthusamarus.
Examining Body: Post-graduate School, University of Ibadan.
Year of Completion: In view.

Student’s name: OLOKE, Oluwakemi Marvellous
Project title: Molecular mechanism of antiplasmodial actions and mitochondrial dynamics of compounds purified from Funtumiaelastica
Examining Body: Post-graduate School, University of Ibadan.
Year of Completion: In view.

Grants

Not Available

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Other Interests/Hobbies

 OLANLOKUN interestsandhobbies

I have vested interest in nature and what it promises to give. I am keenly interested in taking care of animals and like watching animal documentaries and sports. I am also interested in farming and keep a small orchard. My hobby isdraught board game.


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