1. Role: Department Chairperson. Scope: Department. Description: Pharmaceutical Sciences, University of Oklahoma College of Pharmacy. Date: 2009.
Kelly M. Standifer, Ph.D.
Professor and Chair
Pharmaceutical Sciences
Phone (405) 271-6593 x47333
Fax (405) 271-7505
Office CPB 329
Summary
Our research goals are to develop a therapeutic treatment for traumatic brain injury (TBI) and co-morbid conditions such as post-traumatic stress disorder (PTSD), impaired learning and memory and pain. The newest member of the opioid receptor family, nociceptin/orphanin FQ peptide receptor (NOP; also known as ORL1 and KOR3), and its endogenous agonist, nociceptin/orphanin FQ (N/OFQ), bi-directionally modulate CNS and immune system functions, including (but not limited to) pain sensitivity, anxiety, cognition and monocyte chemotaxis. N/OFQ appears to function as a physiological modulator, trying to restore homeostasis. Over the last 15 years, our lab has examined the role of N/OFQ/NOP in three devastating physiological conditions: TBI, PTSD and chronic pain. We found that N/OFQ levels increase in various brain regions, CSF and/or serum over time following TBI, traumatic stress or chronic nerve injury. We hypothesize that the N/OFQ/NOP system becomes dysregulated, either in response to, or because of these conditions. We’ve employed a variety of approaches to study receptor activity and NOP/N/OFQ expression in vitro and in vivo. This includes use of cell lines from different cell types, and male and female rats that express functional or non-functional NOP receptors. We found that elevated levels of N/OFQ are associated with vestibular deficits following TBI, and with allodynia following exposure to a traumatic stress. A single, acute injection of NOP antagonist within 30 min of TBI delayed the appearance of vestibular deficits but prevented the development of oxidative damage 9 days later (Awwad et al., 2018). Similarly, administration of NOP antagonist 7 days following exposure to traumatic stress reverses persistent hyperalgesia caused by traumatic stress (Zhang et al., 2015). Loss of a functional NOP receptor in male rats was protective from traumatic stress-induced hyperalgesia, failed to provide the same relief in female rats (Zhang et al., 2019), and reduced the severity and recovery time from TBI in male and female rats (Al Yacoub et al., 2024). As a result, we utilize two different models of TBI (focal impact and concussive) and a model of PTSD to interrogate the ability of NOP receptor partial agonists prevent or reverse TBI- and/or PTSD-induced vestibular and cognitive deficits, anxiety-like behaviors and hyperalgesia.
Publications & Presentations
- 66. Standifer K, Murthy L R, Kinouchi K, Steele L, Pasternak G W. Affinity labeling of mu and kappa receptors with naloxone benzoylhydrazone. Mol. Pharmacol.. 1991; 39 : 290–298
67. Arjune D, Standifer K, Pasternak G W, Bodnar R J. Reduction by central beta-funaltrexamine of food intake in rats under freely-feeding, deprivation and glucoprivic conditions. Brain Res.. 1990; 535 : 101–109
68. Kinouchi K, Standifer K, Pasternak G W. Modulation of mu 1, mu 2, and delta opioid binding by divalent cations. Biochem. Pharmacol.. 1990; 40 : 382–384
69. Standifer K, Pitha J, Baker S P. Carbostyril-based beta-adrenergic agonists: evidence for long lasting or apparent irreversible receptor binding and activation of adenylate cyclase activity in vitro. Naunyn Schmiedebergs Arch. Pharmacol.. 1989; 339 : 129–137
70. Paul D, Standifer K, Inturrisi C E, Pasternak G W. Pharmacological characterization of morphine-6 beta-glucuronide, a very potent morphine metabolite. J. Pharmacol. Exp. Ther.. 1989; 251 : 477–483
Grants
- 11. Development of a dose-exposure response relationship for detection of opioid tolerance in critically-ill children receiving fentanyl continuous infusions. Misc Non-Federal. Start Date: 2015. End Date: 2017.
12. Modulation of Inflammatory Mechanisms Underlying Chronic Pain of Posttraumatic Stress Disorder: Prevention and Treatment. Misc Non-Federal. Start Date: 2015. End Date: 2016.
13. Multi-Modal Protein and RNA Visualization and Quantification. Misc Non-Federal. Start Date: 2015. End Date: 2016.
14. Neuroinflammatory mechanisms drive traumatic stress-associated pain hypersensitivity. Misc Non-Federal. Start Date: 2015. End Date: 2016.
15. Development of metabolic syndrome in an animal model of PTSD. Misc Non-Federal. Start Date: 2015. End Date: 2015.
Awards and Honors
- 1. OU College of Pharmacy. Richard T. Anderson Endowed Chair in Neuroscience. Date: 2016.
2. University of Houston College of Pharmacy. Faculty Research Excellence Award. Date: 2003.
3. University of Houston College of Pharmacy. Faculty Achievement Award. Date: 2001.
4. The Scientist. 'Hot Paper' Recognition. Date: 1996.
5. University of Houston College of Pharmacy. Faculty Achievement Award. Date: 1996.
Education
- 1. Degree: Postdoctoral Training. Memorial Sloan-Kettering Cancer Center. Date: 1990.
2. Degree: Ph D. University of Florida . Date: 1988.
3. Degree: BS. Duke University. Date: 1984.
4. Degree: Associate of Natural Science. St. Gregory's College. Date: 1982.
Administrative Assignments
2. Role: Department Vice-Chair. Scope: Department. Description: Dept Pharmacological & Pharmaceutical Sciences, University of Houston, College of Pharmacy. Date: 2003.