![CeCe Hillard, PhD](/-/media/MCW/Departments/Pharmacology-and-Toxicology/People/CeCe-Hillard_Academic-Profile.jpg?scale=both&w=400&anchor=middlecenter&mode=crop&h=450&la=en&hash=36DAC87FE651B11F51DD5B057E110723)
Cecilia J. Hillard, PhD
Associate Dean for Research; Professor; Director, Neuroscience Research Center; G. Frederick Kasten, Jr. Endowed Chair in Parkinson’s Disease Research
Locations
- Pharmacology and Toxicology
Contact Information
General Interests
Education
BS, Chemistry, University of Virginia, 1977
Biography
Dr. Hillard was named Associate Dean for Research in November 2015 after serving eight months as co-Interim Senior Associate Dean for Research. She has served as director of the Neuroscience Research Center since its inception in 2010. She was also Inaugural Director of the Neuroscience Graduate Training Program from 1996-2010. As a highly active researcher, Dr. Hillard’s laboratory is primarily focused on the pharmacology and biochemistry of the cannabinoids and endocannabinoids. Her significant bibliography and frequent invitations to present attest to her reputation as a leader in her field. Dr. Hillard is an MCW graduate and a true advocate for the Basic Sciences. Frequently named an Outstanding Medical Student Teacher, Dr. Hillard takes an active role in training and mentorship, receiving MCW’s highest honor, the Distinguished Service Award, in 2011.
Dr. Hillard was recently awarded the Lifetime Achievement Award from the International Cannabinoid Research Society. Dr. Hillard is a member of both the Society of Teaching Scholars and the Society for Research Excellence at MCW.
Research Experience
- Anxiety
- Brain
- Cannabidiol
- Cannabinoid Receptor Agonists
- Cannabinoid Receptor Modulators
- Cannabinoids
- Carrier Proteins
- Cells, Cultured
- Cocaine
- Corticosterone
- Depression
- Endocannabinoids
Research Interests
Marijuana has been used by humans for more than 2,500 years as a medicinal agent and social drug. Cannabinoids are the chemicals in marijuana that are responsible for its effects on the body. A long-standing interest of our laboratory is the study of the mechanisms by which the cannabinoids affect the function of the brain. Delta-9-tetrahydrocannabinol (THC) is the cannabinoid in marijuana that is responsible for its mood- and sensation-altering effects. THC targets two receptors: the CB1 receptor present on neurons and the CB2 receptor that is present primarily on immune cells. Although THC targets these receptors when a person is exposed to the drug from the outside, we know that at least two “endogenous” (or, from the self) molecules also target these receptors. These two molecules are named the endocannabinoids. Our research focuses on the cannabinoids, the receptors with which they interact and the role of the endocannabinoids in brain function.
We have three major research projects:
Studies of the biochemical mechanisms involved in the synthesis, release and degradation of the endocannabinoids
At least two lipid molecules are thought to act as endocannabinoids, anandamide and 2-arachidonoylglycerol. Both can be synthesized by neurons but our knowledge of the mechanisms that regulate their synthesis is lacking in detail. One goal of our work is to develop inhibitors of these pathways to help us understand the physiological roles of endocannabinoids. We are also studying the processes by which the endocannabinoids are inactivated. We know that they are catabolized by enzymes and that they are substrates for transporters that act in plasma membranes. One of our goals is to biochemically understand these processes and to develop inhibitors.
Studies of the role of endocannabinoid signaling in the regulation of mood and responses to stress
Several laboratories, including ours, have demonstrated that one very important function of the endocannabinoids is to regulate the response of the brain to stress. Animals and humans need to cope with physical and psychological stresses in order to survive, but stress responses have a cost. For example, we know that long term stress exposure results in depression and post traumatic stress disorder in humans. The endogenous cannabinoid system is a stress buffer, it turns down the hormonal and behavioral responses to stress. In addition, the endocannabinoid system is itself turned on or, in some cases, turned off by stress. Our goal in these studies is to examine the mechanistic relationships between stress and the endocannabinoids. While most of our studies are carried out using rodent models, we are also exploring these processes in human subjects exposed to periods of psychological stress through collaborations with other investigators.
Roles of cannabinoids in regulation of the immune response
Signaling through the CB2 receptor has been shown to reduce activation of the immune system. Although immune cell activation is vital to fight infections, excess or inappropriate immune activation contributes to many important and devastating diseases, including multiple sclerosis and graft-versus-host disease, which can occur after bone marrow transplants to treat cancer. Our laboratory is exploring the roles of CB2 receptors and the phytocannabinoid, cannabidiol, in neuroinflammation and graft-versus-host disease models.
Publications
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(Geier TJ, Atkinson SN, Pan AY, Mantz-Wichman M, Jazinski-Chambers K, Hillard CJ, deRoon-Cassini TA.) J Affect Disord. 2024 Sep 15;361:528-535 PMID: 38914163 SCOPUS ID: 2-s2.0-85196827087 06/25/2024
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(Guenther KG, Lin X, Xu Z, Makriyannis A, Romero J, Hillard CJ, Mackie K, Hohmann AG.) Biomed Pharmacother. 2024 Jul;176:116879 PMID: 38850666 PMCID: PMC11209786 SCOPUS ID: 2-s2.0-85195323734 06/09/2024
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(Venkatesan T, Hillard CJ, Ayer L, Arumugam S, Culp S, Vyas M, Gofar K, Petrova A, Palsson OS.) Clin Transl Gastroenterol. 2024 Jul 01;15(7):e00711 PMID: 38713142 PMCID: PMC11272346 SCOPUS ID: 2-s2.0-85193314896 05/07/2024
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(Cheng G, Hardy M, Hillard CJ, Feix JB, Kalyanaraman B.) Commun Biol. 2024 May 30;7(1):668 PMID: 38816577 PMCID: PMC11139878 SCOPUS ID: 2-s2.0-85194991828 05/31/2024
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(Moe A, Rayasam A, Sauber G, Shah RK, Doherty A, Yuan CY, Szabo A, Moore BM 2nd, Colonna M, Cui W, Romero J, Zamora AE, Hillard CJ, Drobyski WR.) J Clin Invest. 2024 Apr 25;134(11) PMID: 38662453 PMCID: PMC11142740 SCOPUS ID: 2-s2.0-85195012384 04/25/2024
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(Guenther KG, Lin X, Xu Z, Makriyannis A, Romero J, Hillard CJ, Mackie K, Hohmann AG.) bioRxiv. 2024 Mar 10 PMID: 38496640 PMCID: PMC10942397 03/18/2024
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(Comai S, Nunez N, Atkin T, Ghabrash MF, Zakarian R, Fielding A, Saint-Laurent M, Low N, Sauber G, Ragazzi E, Hillard CJ, Gobbi G.) BMC Med. 2024 Jan 25;22(1):33 PMID: 38273283 PMCID: PMC10809514 SCOPUS ID: 2-s2.0-85182980042 01/26/2024
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Effect of trauma type and trauma burden on self-efficacy for physical exercise in military veterans
(Davis KE, Bennett MM, Hillard CJ, Whittle J, Franco Z, Bollaert RE, Fitzgerald JM.) Trauma (United Kingdom). 2024 SCOPUS ID: 2-s2.0-85186393424 01/01/2024
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(Hill MN, Haney M, Hillard CJ, Karhson DS, Vecchiarelli HA.) Psychol Med. 2023 Nov;53(15):7006-7024 PMID: 37671673 PMCID: PMC10719691 SCOPUS ID: 2-s2.0-85170686532 09/06/2023
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(Moe A, Rayasam A, Sauber G, Shah RK, Yuan CY, Szabo A, Moore BM, Colonna M, Cui W, Romero J, Zamora AE, Hillard CJ, Drobyski WR.) bioRxiv. 2023 Aug 14 PMID: 37645843 PMCID: PMC10462026 08/30/2023
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(Sirotiak Z, Gallagher BT, Smith-Hernandez CA, Showman LJ, Hillard CJ, Brellenthin AG.) PLoS One. 2023;18(12):e0291845 PMID: 38039265 PMCID: PMC10691681 SCOPUS ID: 2-s2.0-85178330078 12/01/2023
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Endocannabinoids, cortisol, and development of post-traumatic psychopathological trajectories.
(Jayan D, Timmer-Murillo S, Fitzgerald JM, Hillard CJ, de Roon-Cassini TA.) Gen Hosp Psychiatry. 2023;85:199-206 PMID: 37956620 PMCID: PMC10843734 SCOPUS ID: 2-s2.0-85176356508 11/14/2023