Andrew Gow, Ph.D.

Professor Rutgers University – Ernest Mario School of PharmacyEOHSI – Toxicology
Work William Levine Hall Room 009 160 Frelinghuysen Road Piscataway NJ 08854 Work Phone: 732-445-4612 Work Fax: 732-445-0119 Website: Dr. Gow’s Bio Page
Photo of Andrew Gow Ph.D.

Biographical Info


  • BSc,  (Hons)  University of Edinburgh, Edinburgh, Scotland, UK
  • MEd,  Temple University, Philadelphia, PA
  • PhD, Temple University, Philadelphia, PA
  • Post-Doc, University of Pennsylvania, Philadelphia, PA

Research Areas

Mechanisms of nitric oxide signaling in a wide variety of pathophysiological conditions; molecular mechanisms involved in controlling nitric oxide signaling and the role of nitric oxide in cardiopulmonary diseases such as emphysema, acute lung injury, bronchopulmonary dysplasia, sickle cell disease and diabetes; Nitric oxide in inflammatory cells such as macrophages and microglia.


Our laboratory investigates mechanisms of Nitric Oxide signaling in a wide variety of pathophysiological conditions.  We seek to understand the molecular mechanisms involved in controlling Nitric Oxide signaling and answer the question as to how nature uses such a simple molecule to control a multitude of biological processes and in almost every organism.  In particular, we investigate the role of Nitric Oxide in cardiopulmonary diseases such as emphysema, acute lung injury, bronchopulmonary dysplasia, sickle cell disease and diabetes.  We are particularly interested in the function of Nitric Oxide in inflammatory cells such as macrophages and microglia.  It is thought that by better understanding the mechanisms involved in Nitric Oxide signaling that we can design appropriate pharmacological interventions for human diseases in which Nitric Oxide metabolism is disrupted.

Research Highlights

  • S-nitrosylation of pulmonary collectins
  • Role of nitric oxide in lung disease
  • Mechanisms regulating nitric oxide biosynthesis

Scholarly Activities

  • 2001, Florence R.C. Murray Fellowship
  • 2000, Translational Medicine Award, Duke University
  • 1998, Chartered Chemist, Royal Society of Chemistry
  • 1997, Young Investigator Award, International Nitric Oxide Society
  • 1996, Young Investigator Award, Oxygen Society
  • 1995-97, National Research Service Award, National Institutes of Health-NHLBI in Lung Cell and Molecular Biology
  • 1993-95, Russell Conwell Research Fellowship

Recent Publications

  1. Sunil, VR, Vayas, KN, Radbel, J, Abramova, E, Gow, A, Laskin, JD, Laskin, DL. Impaired energy metabolism and altered functional activity of alveolar type II epithelial cells following exposure of rats to nitrogen mustard. Toxicol Appl Pharmacol. 2022; :116257. doi: 10.1016/j.taap.2022.116257. PubMed PMID:36174670
  2. Murray, A, Banota, T, Guo, GL, Smith, LC, Meshanni, JA, Lee, J, Kong, B, Abramova, EV, Goedken, M, Gow, AJ et al.. Farnesoid X receptor regulates lung macrophage activation and injury following nitrogen mustard exposure. Toxicol Appl Pharmacol. 2022;454 :116208. doi: 10.1016/j.taap.2022.116208. PubMed PMID:35998709
  3. Stevenson, ER, Wilkinson, ML, Abramova, E, Guo, C, Gow, AJ. Intratracheal Administration of Acyl Coenzyme A Acyltransferase-1 Inhibitor K-604 Reduces Pulmonary Inflammation Following Bleomycin-Induced Lung Injury. J Pharmacol Exp Ther. 2022;382 (3):356-365. doi: 10.1124/jpet.122.001284. PubMed PMID:35970601 PubMed Central PMC9426763
  4. Xu, S, Karmacharya, N, Cao, G, Guo, C, Gow, A, Panettieri, RA Jr, Jude, JA. Obesity elicits a unique metabolomic signature in human airway smooth muscle cells. Am J Physiol Lung Cell Mol Physiol. 2022;323 (3):L297-L307. doi: 10.1152/ajplung.00132.2022. PubMed PMID:35787188
  5. Golden, TN, Venosa, A, Gow, AJ. Cell Origin and iNOS Function Are Critical to Macrophage Activation Following Acute Lung Injury. Front Pharmacol. 2021;12 :761496. doi: 10.3389/fphar.2021.761496. PubMed PMID:35145401 PubMed Central PMC8822172
  6. Golden, T, Murray, A, Venosa, A, Gow, AJ. Comprehensive dataset to assess morphological changes subsequent to bleomycin exposure. Data Brief. 2021;37 :107270. doi: 10.1016/j.dib.2021.107270. PubMed PMID:34430679 PubMed Central PMC8365314
  7. Massa, CM, Liu, Z, Taylor, S, Pettit, AP, Stakheyeva, MN, Korotkova, E, Popova, V, Atochina-Vasserman, EN, Gow, AJ. Biological Mechanisms of S-Nitrosothiol Formation and Degradation: How Is Specificity of S-Nitrosylation Achieved?. Antioxidants (Basel). 2021;10 (7):. doi: 10.3390/antiox10071111. PubMed PMID:34356344 PubMed Central PMC8301044
  8. Venosa, A, Smith, LC, Gow, AJ, Zarbl, H, Laskin, JD, Laskin, DL. Macrophage activation in the lung during the progression of nitrogen mustard induced injury is associated with histone modifications and altered miRNA expression. Toxicol Appl Pharmacol. 2021;423 :115569. doi: 10.1016/j.taap.2021.115569. PubMed PMID:33971176 PubMed Central PMC8496734
  9. Venosa, A, Gow, JG, Taylor, S, Golden, TN, Murray, A, Abramova, E, Malaviya, R, Laskin, DL, Gow, AJ. Myeloid cell dynamics in bleomycin-induced pulmonary injury in mice; effects of anti-TNFα antibody. Toxicol Appl Pharmacol. 2021;417 :115470. doi: 10.1016/j.taap.2021.115470. PubMed PMID:33647319
  10. Murray, A, Gow, AJ, Venosa, A, Andres, J, Malaviya, R, Adler, D, Yurkow, E, Laskin, JD, Laskin, DL. Assessment of mustard vesicant lung injury and anti-TNF-α efficacy in rodents using live-animal imaging. Ann N Y Acad Sci. 2020;1480 (1):246-256. doi: 10.1111/nyas.14525. PubMed PMID:33165947 PubMed Central PMC7968421
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Categories: Faculty, Toxicology, Member, Tox Member
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