Abstract
The prevalence of methamphetamine (METH) use is estimated at ∼35 million people worldwide, with over 10
million users in the United States (US). Chronic METH abuse and dependence expose the user to a diverse
range of adverse physical and cognitive health consequences. The administration of drugs such as METH via
injection delivers almost immediate effects of euphoria due to the substantial accumulation of dopamine in the
central nervous system. Significantly, heavy daily users of METH frequently develop formication, a sensation
akin to insects crawling on or under the skin. The result of formication is that users engage in constant skin
“picking,” often causing the formation of ulcers that have delayed closure and frequently scar. A marked lack of
hygiene among users may also be correlated to higher rates of skin infections. Wounds associated with METH
users are an important wound care problem at respite centers and healthcare institutions. In addition, the cost
of treatment for METH-associated chronic wounds per year is a heavy economic burden to our healthcare
system. Although there is substantial information on the behavioral and cognitive defects caused by METH in
drug users, there is a dearth of knowledge regarding its impact on wound healing and inflammation. My
preliminary data shows that METH treated mice had decreased wound healing. Also, METH increases IL-6
production in skin tissue and elevated levels of this cytokine may have a direct pathogenic role in inflammation.
IL-6 may be regulated by dopamine which can activate inflammatory cells. Hence, I hypothesize that METH
alters leukocyte recruitment and also enhances IL-6 production via dopaminergic activation
exacerbating the inflammatory response leading to delay wound healing. This R15 Academic Research
Enhancement Award (AREA) is designed to make major contributions in elucidating the mechanisms by which
METH alters inflammatory responses and interferes with wound healing, leading to chronic wounds susceptible
to microbial infections. There are two aims proposed: (1) investigate the impact of METH on wound
polymorphonuclear leukocytes recruitment and repair in vivo; and (2) assess the role of METH on IL-6
production in the setting of wound healing and inflammation in vivo. I believe this project is of considerable
significance in the fields of drug abuse, dermatology, and immunity. It is anticipated that this interdisciplinary
program may advance the future development of practical therapeutic interventions for the management of
chronic wounds in drug users. Furthermore, an AREA award would be the primary support for my research at
the NYIT College of Osteopathic Medicine, strengthening the institution’s research environment and exposing
significantly more of our students to biomedical research, which will greatly enhance their potential for pursuing
scientific and health‐related careers.