Nader H. Moniri, Ph.D .:. Home

Contact Information:

3001 Mercer University Dr

239 Moye Center

Atlanta, GA 30341

(678)-547-6246

moniri_nh at mercer.edu

Education and Training

Post-Doctoral Fellow, Pharmacology

Duke University Medical Center, Durham, NC

Ph.D., Pharmaceutical Sciences

University of North Carolina, Chapel Hill, NC

B.S., Biological Sciences / Chemistry

Georgia State University, Atlanta, GA

Academic Appointments

Professor of Biomedical Sciences, School of Medicine, Mercer University

Professor of Pharmaceutical Sciences, College of Pharmacy, Mercer University

Associate Dean for Research, College of Pharmacy, Mercer University

Bio

Dr. Moniri serves as Associate Dean for Research and Professor of Pharmaceutical Sciences in the College of Pharmacy. He is also appointed as Professor of Biomedical Sciences in the School of Medicine. He received a B.S. in Biological Sciences from Georgia State University and a Ph.D. in Pharmaceutical Sciences from the Division of Medicinal Chemistry at the School of Pharmacy at UNC - Chapel Hill. Trained primarily in molecular pharmacology and medicinal chemistry, Dr. Moniri completed a post-doctoral fellowship at Duke University Medical Center and joined the faculty at the College of Pharmacy at Mercer in 2006. Click here for Dr. Moniri's Complete CV.

Laboratory Research Focus Areas:

Dr. Moniri's training has focused on molecular pharmacology and signal transduction of G protein-coupled receptors (GPCR) as well as the design and development of novel agents which modulate GPCR function.

Current research interests include characterization of free-fatty acid (FFA) GPCRs, and their role in human health and disease. Our current projects focus on the role of FFA receptors, including the long-chain FFA receptors FFA1/GPR40 and FFA4/GPR120, as well as the short-chain FFA receptors FFA2/GPR43 and FFA3/GPR41 in metabolism, neurodegeneration, inflammation, and cancers.

An NIH/NHLBI-funded grant also supports projects that seeks to understand the role of reactive oxygen species (ROS) in regulating the β2-adrenergic receptor (β2AR), which is critical in the treatment of airway disorders such as asthma and COPD.

Another recent NIH grant in collaboration with Dr. Clint Canal supports the study of the mechanisms of the drug of abuse xylazine on α2-adrenergic receptors. Along with Dr. Canal, Dr. Moniri is also co-founder of Channel Therapeutics, a biopharmaceutical company that seeks to develop drugs that act with high selectivity at muscarinic acetylcholine receptors for treatment of a variety of brain, gastrointestinal, urinary, and airway disorders.

Dr. Moniri's lab also collaborates with Dr. Raquib Hasan on three American Heart Association and one NIH-funded projects that examine the roles of various intracellular signaling pathways in hypertension.

For more detailed information on research in the Moniri lab, click here.

Teaching:

Dr. Moniri currently teaches physiology, pathophysiology, pharmacology, and medicinal chemistry within various systems and disorders in the Doctor of Pharmacy (Pharm.D.) curriculum at the College of Pharmacy.

PharmD courses taught in include Musculoskeletal Disorders and Pain (P3), Endocrine Disorders (P2), Nervous System Disorders (P3), and Infectious Diseases (P2).

For more detailed information on teaching, click here.

	Peer-Reviewed Publications:
	(Click here for PubMed listing of publications)
	Teyani RL, Moghaddam F, Moniri NH. ROS-mediated regulation of β2AR function: Does oxidation play a meaningful role towards β2-agonist tachyphylaxis in airway obstructive diseases? Biochemical Pharmacology. 226:116403, 1-7, 2024. PMID: 38945277 Singh K, Teyani RL, Moniri NH. Agonists and hydrogen peroxide mediate hyperoxidation of β2-adrenergic receptor in airway epithelial cells: Implications for tachyphylaxis to β2-agonists in constrictive airway disorders. Biomedicine and Pharmacotherapy, 168:115763, 1-13, 2023. PMID: 37865997 Teyani R and Moniri NH. Gut feelings in the islets: The role of the gut microbiome and the FFA2 and FFA3 receptors for short chain fatty acids on β-cell function and metabolic regulation. British Journal of Pharmacology, 180:3113-3129, 2023. PMID: 37620991 Menon SN, Daniel ML, Zerin F, Ezewudo E, Simon NP, Green AJ, Pandey A, Mackay CE, Hafez S, Moniri NH, Hasan R. Neflamapimod inhibits endothelial cell activation, adhesion molecule expression and leukocyte attachment by inhibiting p38 MAPKα and NF-κB signaling. Biochemical Pharmacology. 214:115683, 1-14, 2023. PMID: 37429422 Karmokar PF and Moniri NH. Free-fatty acid receptor-1 (FFA1/GPR40) promotes papillary RCC proliferation and tumor growth via Src/PI3K/AKT/NF-κB but suppresses migration by inhibition of EGFR, ERK1/2, STAT3 and EMT. Cancer Cell International, 23:126, 1-19, 2023. PMID: 37355607 Thurston MM, Moniri NH, Bowen JP, Winkles CL, Miller SW. Managing the “Three Cs" of Academic Literature Authorship: Contributions, Credit, and Conflict. American Journal of Pharmaceutical Education. 87: 100009, 1-4, 2023. PMID: 37288678 Karmokar PF and Moniri NH. Free-Fatty Acid Receptor-4 (FFA4/GPR120) differentially regulates migration, invasion, proliferation and tumor growth of papillary renal cell carcinoma cells. Biochemical Pharmacology. 213:115590, 1-13, 2023. PMID: 37201877 Rizzo AR and Moniri NH. Omadacycline for management of Mycobacterium abscessus infections: A review of its effectiveness, place in therapy, and considerations for use. BMC Infectious Diseases. 22(1):874, 1-11, 2022. PMID: 36419143 Karmokar PF and Moniri NH. Oncogenic signaling of the Free-Fatty Acid Receptors FFA1 and FFA4 in human breast carcinoma cells. Biochemical Pharmacology. 206:115308, 1-10, 2022. PMID: 36309079 Singh K, Senatorov IS, Cheshmehkani A, Karmokar PF, Moniri NH. The skeletal muscle relaxer cyclobenzaprine is a potent non-competitive antagonist of histamine H1 receptors. Journal of Pharmacology and Experimental Therapeutics. 380(3):202-209, 2022. PMID: 34992159 denotes equal authorship. Moniri NH* and Farah Q. Short-chain free-fatty acid G protein-coupled receptors in colon cancer. Biochemical Pharmacology.186:114483, 2021. Senatorov IS, Cheshmehkani A, Burns RN, Singh, K, Moniri NH. Carboxy-terminal phosphoregulation of the long splice isoform of Free-Fatty Acid Receptor-4 mediates β-arrestin recruitment and signaling to ERK1/2. Molecular Pharmacology. 97:304-313, 2020. Rambacher KM and Moniri NH. Cysteine redox state regulates human β2-adrenergic receptor binding and function. Scientific Reports. 10:2934, 1-15, 2020. Chitre NM, Wood BJ, Ray A, *Moniri NH,** Murnane KS. Docosahexaenoic acid protects motor function and increases dopamine synthesis in a rat model of Parkinson's disease via mechanisms associated with increased protein kinase activity in the striatum. Neuropharmacology.* 167:107976, 2020. * denotes co-senior authors. Rambacher KM and Moniri NH. The β2-adrenergic receptor-ROS signaling axis: An overlooked component of β2AR function? Biochemical Pharmacology. 171: 113690, 2020. Chitre N, Moniri NH, Murnane KS. Omega-3 Fatty Acids as Druggable Therapeutics for Neurodegenerative Disorders. CNS & Neurological Disorders - Drug Targets. 18(10):735-749, 2019. Moniri NH. Reintroduction of quazepam: an update on comparative hypnotic and adverse effects. International Clinical Psychopharmacology. 34(6):275-285, 2019. Murnane KS, Guner OF, Bowen JP, Rambacher KM, Moniri NH, Murphy TJ, Daphney CM, Oppong-Damoah A, Rice KC. The adrenergic receptor antagonist carvedilol interacts with serotonin 2A receptors both in vitro and in vivo. Pharmacology Biochemistry and Behavior. 181:37-45, 2019. Moniri NH, Momary KM, McMahon TJ, Nayee E. Statin-associated Achilles tendon rupture and reproducible bilateral tendinopathy upon repeated exposure. Mayo Clinic Proceedings. 93(10):1531-1532, 2018. Senatorov IS and Moniri NH. The role of free-fatty acid receptor-4 (FFA4) in human cancers and cancer cell lines. Biochemical Pharmacology. 150:170-180, 2018. Cheshmehkani A, Senatorov IS, Dhuguru J, Ghoneim O, Moniri NH. Free-fatty acid receptor-4 (FFA4) modulates ROS generation and COX-2 expression via the C-terminal β-arrestin phosphosensor in Raw264.7 macrophages.Biochemical Pharmacology. 146:139-150, 2017. Moniri NH. Free-fatty acid receptor-4 (GPR120): cellular and molecular function and its role in metabolic disorders. Biochemical Pharmacology. 110-111:1-15, 2016. Cheshmehkani A, Senatorov IS, Kandi P, Singh M, Britt A, Hayslett R, Moniri NH. Fish and flax seed oil supplemented diets increase FFAR4 expression in the rat colon. Inflammation Research. 64(10):809-15, 2015. Singh M and Moniri NH. Reactive oxygen species as β-adrenergic receptor signal transducers. Journal of Pharmaceutics and Pharmacology. 2(1): 8-15, 2014. Burns RN, Singh M, Senatorov IS, Moniri NH. Mechanisms of homologous and heterologous phosphorylation of FFA receptor 4 (GPR120): GRK6 and PKC mediate phosphorylation of Thr347, Ser350, and Ser357 in the C-terminal tail. Biochemical Pharmacology. 87:650-659, 2014. Ryan GJ, Moniri NH, Smiley DD. Clinical effects of once-weekly exenatide for the treatment of type 2 diabetes mellitus. American Journal of Health-System Pharmacy. 70(13):1123-1131, 2013. Gleason BL, Siracuse MV, Moniri NH, Birnie CR, Okamoto CT, Crouch MA. Evolution of Preprofessional Pharmacy Curricula. American Journal of Pharmaceutical Education. 77(5):95; 1-8, 2013. Singh M and Moniri NH. Reactive oxygen species are required for β2-adrenergic receptor-β-arrestin interactions and signaling to ERK1/2. Biochemical Pharmacology. 84:661-669, 2012. Burns RN and Moniri NH. Agonist- and Hydrogen peroxide- mediated oxidation of the β2 adrenergic receptor: evidence of receptor S-sulfenation as detected by a modified biotin switch assay. Journal of Pharmacology and Experimental Therapeutics. 339(3):914-921, 2011. Wang Z, Humphrey C, Frilot N, Wang G, Nie Z, Moniri NH, Daaka Y. Dynamin2- and endothelial nitric oxide synthase-regulated invasion of bladder epithelial cells by uropathogenic Escherichia coli. Journal of Cell Biology. 10;192(1):101-10, 2011. Burns RN and Moniri NH. Agonism with the omega-3 fatty acids alpha-linolenic acid and docosahexaenoic acid mediates phosphorylation of both the short and long isoforms of the human GPR120 receptor. Biochemical and Biophysical Research Communications. 396: 1030-1035, 2010. Bagchi G, Wu J, French J, Kim J, Moniri NH, Daaka Y. Androgens transduce the Gαs-mediated activation of protein kinase A in prostate cells. Cancer Research. 68: 3225-3231, 2008. Moniri NH and Daaka Y. Agonist-stimulated reactive oxygen species formation regulates β2-adrenergic receptor signal transduction. Biochemical Pharmacology. 74: 64-73, 2007. Booth RG and Moniri NH. Novel ligands stabilize stereo-selective conformations of the histamine H1 receptor to activate catecholamine synthesis. Inflammation Research. 56:S1-2, 2007. Moniri NH and Booth RG. Role of PKA and PKC in Histamine H1 Receptor-Mediated Activation of Catecholamine Neurotransmitter Synthesis. Neuroscience Letters. 407:249-253, 2006. Bagchi G, Moniri NH, Daaka Y. Androgen Receptor. AfCS-UCSD-Nature Molecule Pages. 2006. (doi:10.1038/mp.a003790.01) Guo R, Kasbohm EA, Arora P, Sample CJ, Baban B, Sud N, Sivashanmugam P, Moniri NH, Daaka Y. Expression and function of lysophosphatidic acid LPA1 receptor in prostate cancer cells. Endocrinology. 147:4883-4892, 2006. Wang G, Moniri NH, Ozawa K, Stamler JS, Daaka Y. Nitric oxide regulates endocytosis by S-nitrosylation of dynamin. Proceedings of the National Academy of Sciences, USA. 103(5):1295-1300, 2006. Booth RG and Moniri NH. Ligand-directed multifunctional signaling of histamine H1 receptors. Inflammation Research. 54:S44-45, 2005. Moniri NH, Covington-Strachan DW, Booth RG. Ligand-directed functional heterogeneity of histamine H1 receptors: Novel agonists selectively activate and block H1 mediated phospholipase C and adenylyl cyclase signaling in CHO cells. Journal of Pharmacology and Experimental Therapeutics. 311:274-281, 2004. Moniri NH and Booth RG. Functional heterogeneity of histamine H1 receptors. Inflammation Research. 53:S71-72, 2004. Booth RG, Moniri NH, Bakker RA, Choksi NY, Nix WB, Timmerman H, Leurs R. A novel phenylaminotetralin radioligand reveals a sub-population of histamine H1 receptors. Journal of Pharmacology and Experimental Therapeutics. 302:328-336, 2002.
	Book Chapters:
	Moniri NH. Drugs used to induce/support sedation or anesthesia. Foye’s Principles of Medicinal Chemistry. Chapter 12. Roche VF and Zito SW, Lemke TL, Williams DA, eds. Lippincott, Williams, & Wilkins, Philadelphia, PA, 8th ed., 2019. Moniri NH. Sedative-Hypnotics. Foye’s Principles of Medicinal Chemistry. Lemke TL and Williams DA, eds. Lippincott, Williams, & Wilkins, Baltimore, MD, 7th ed., 2012.
	Published Proceedings:
	Hasan R, Ezewudo E, Zerin F, Menon S, Simon N, Moniri NH, Nguyen TT, Chougule MB, Rahman T. Indole-3 acetic acid: a novel dual-action inhibitor of the endothelin system for treating hypertension. Hypertension, 80:AP318, 2023. Ezewudo E, Menon S, Zerin F, Moniri NH, Nguyen T, Kashikar R, Chougule M, Rahman T, Hasan R. A novel small molecule inhibitor of vascular endothelin signaling and hypertension. Physiology, 38:S1, 2023. Moniri NH, Senatorov IS, Cheshmehkani A, Karmokar P, Singh K. The skeletal muscle relaxer cyclobenzaprine is a potent non-competitive histamine H1 receptor antagonist. The FASEB Journal, 35 (S1), 2021. Presented virtually at Experimental Biology (ASPET), 2021. Karmokar PF and Moniri NH. Diverse Roles of G-Protein-Coupled Receptor 40 (GPR40/FFA1) and GPR120 (FFA4) in the Regulation of Cell Growth and Motile Activities in Renal Cell Carcinoma (RCC). The FASEB Journal, 35 (S1), 2021. Presented virtually at Experimental Biology (ASPET), 2021. Singh K and Moniri NH. Differential Modulation of β2AR Mediated cAMP/PKA/CREB Signaling Cascade in Normal versus Asthmatic Airway Epithelial Cells. The FASEB Journal, 35 (S1), 2021. Presented virtually at Experimental Biology (ASPET), 2021. Rambacher KM and Moniri NH. Redox deficient cysteine residues impair β2-adrenergic receptor function. The FASEB Journal, 33(1S):668.3. Presented at Experimental Biology (ASPET), Orlando, FL, 2019. Chitre NM, Wood B, Ray A, Moniri NH, Murnane KS. Assessing the neuroprotective effects of docosahexaenoic acid in 6-hydroxydopamine induced Parkinsonism in rats. The FASEB Journal, 33(1S):501.10. Presented at Experimental Biology (ASPET), Orlando, FL, 2019. Moniri NH and Sambunaris A. The Institute for Advanced Medical Research at Mercer University: Translational and Clinical Research Opportunities for Students. American Journal of Pharmaceutical Education. 82(5): 25. Presented at American Association of Colleges of Pharmacy, Boston, MA, 2018. Rambacher KM and Moniri NH. Ligand Binding to the β2-Adrenergic Receptor Is Dependent Upon Its Oxidation State. The FASEB Journal, 32(1S):555.14. Presented at Experimental Biology (ASPET), San Diego, CA, 2018. Senatorov IS, Cheshmehkani A, Moniri NH. Investigating Phosphorylation Differences in FFA4 Short and Long Isoforms. The FASEB Journal, 32(1S):555.30. Presented at Experimental Biology (ASPET), San Diego, CA, 2018. Cheshmehkani A and Moniri NH. Effects of phosphodefective FFA4 receptor C-terminal mutants on COX-2 expression in macrophages. The FASEB Journal, 31(1S):992.10. Presented at Experimental Biology (ASPET), Chicago, IL, 2017. Spry R, Hibicke M, Rogers D, Rambacher KM, Hayslett R, Moniri N, Murnane K. A new testing paradigm for evaluating motor and non-motor symptoms of 6-hydroxydopamine lesions in rats. The FASEB Journal, 31(1S):662.7. Presented at Experimental Biology (ASPET), Chicago, IL, 2017. Murnane KS, Guner O, Moniri NH, Bowen P. Ligand-based pharmacophore modeling of 5-HT2A receptor biased agonism. The FASEB Journal, 29:768.12. Presented at Experimental Biology (ASPET), Boston, MA, 2015. Singh M and Moniri NH. Role of reactive oxygen species as signal transducers in β2-adrenergic receptor mediated β-arrestin signaling. The FASEB Journal, 28:662.2. Presented at Experimental Biology (ASPET), San Diego, CA, 2014. Singh M and Moniri NH. Brighter side of reactive oxygen species (ROS) revealed in β2 adrenergic receptor-β-arrestin interactions and signaling to ERK1/2. Molecular Biology of the Cell. Presented at the annual meeting of the American Society for Cell Biology, Abstract #592, New Orleans, LA, 2013. Singh M and Moniri NH. Reactive Oxygen Species are required for β2-adrenergic receptor mediated β-arrestin signaling. The FASEB Journal, 26:665.6.Presented at Experimental Biology (ASPET), San Diego, CA, 2012. Burns RN and Moniri NH. Elucidation of the phosphorylation profiles of the long and short isoforms of the omega-3 fatty acid receptor-1 (GPR120). The FASEB Journal, 26:837.7. Presented at Experimental Biology (ASPET), San Diego, CA, 2012. Burns RN and Moniri NH. Agonist-dependent oxidation of the β2 adrenergic receptor: Selective cysteine sulfenic acid formation detected by a modified biotin switch assay. The FASEB Journal, 25:629.7. Presented at Experimental Biology (ASPET),Washington, DC, 2011. Burns RN and Moniri NH. Omega-3 fatty acid mediated phosphorylation of the short and long human GPR120 receptor isoforms. The FASEB Journal, 24:585.6. Presented atExperimental Biology (ASPET),Anaheim, CA, 2010. Moniri NH and Daaka Y. β2-adrenergic receptor mediated generation of reactive oxygen species is a component required for signal transduction, desensitization, and homodimerization. The FASEB Journal, 22:723.6. Presented at Experimental Biology (ASPET),San Diego, CA, 2008.