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University of Houston College of Pharmacy - the STEM Digital Village

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Alcohol Mechanism Project Draws NIH Support for Das<br />

By Lisa Merkl<br />

With <strong>the</strong> ultimate goal to discover a<br />

drug that one day treats alcoholism, UH<br />

<strong>College</strong> <strong>of</strong> <strong>Pharmacy</strong> Assistant Pr<strong>of</strong>essor<br />

Joydip Das is working on pinpointing <strong>the</strong><br />

mechanisms in <strong>the</strong> brain that respond to<br />

alcohol.<br />

Das recently received a three-year,<br />

$450,000 grant from <strong>the</strong> National Institute<br />

on Alcoholism and Alcohol Abuse. In <strong>the</strong><br />

end, his team hopes <strong>the</strong>ir research will<br />

help lead <strong>the</strong>m to a way to prevent people<br />

from drinking to excess.<br />

“Defining targets and elucidating <strong>the</strong><br />

molecular mechanism <strong>of</strong> <strong>the</strong>ir actions is<br />

needed for effective intervention,” Das<br />

said. “Once we understand <strong>the</strong> target,<br />

<strong>the</strong>n we design drugs based on that<br />

target.”<br />

Das explained that addictions are related<br />

to <strong>the</strong> brain, with protein kinase C (PKC)<br />

– particularly <strong>of</strong> <strong>the</strong> PKCε subtype –<br />

being mainly expressed in <strong>the</strong> brain and<br />

playing a key role in this process. Previous<br />

observations have indicated as much as a<br />

75 percent reduction <strong>of</strong> alcohol drinking<br />

in mice using knockout technology,<br />

demonstrating that knocking out <strong>the</strong><br />

PKCε protein cuts desire.<br />

Jerry Powers photo<br />

Assistant Pr<strong>of</strong>essor Joydip Das, Ph.D., has received<br />

a $450,000 grant from <strong>the</strong> National Institute<br />

<strong>of</strong> Alcoholism and Alcohol Abuse to define <strong>the</strong><br />

molecular mechanisms by which alcohols exert<br />

<strong>the</strong>ir action on <strong>the</strong> signaling pathways in <strong>the</strong> brain.<br />

As it’s difficult to pinpoint where alcohol<br />

acts and what its target is, his team’s<br />

objective is to find <strong>the</strong> target and <strong>the</strong>n<br />

determine how it interacts with ion<br />

channels to affect <strong>the</strong> addiction.<br />

“We’re looking at <strong>the</strong> significance <strong>of</strong> <strong>the</strong><br />

interaction between <strong>the</strong> alcohol molecule<br />

and PKCε protein,” Das said. “How <strong>the</strong><br />

alcohol molecule binds with <strong>the</strong> target is<br />

<strong>the</strong> key. This binding has implications in<br />

addiction, so our intent is to design drugs<br />

to curb <strong>the</strong> desire for more than a small<br />

amount <strong>of</strong> alcohol so that people stay<br />

away from excessive drinking.”<br />

Trained at MIT and having worked in <strong>the</strong><br />

anes<strong>the</strong>sia department at Massachusetts<br />

General Hospital, Das has a particular<br />

interest in this area, saying that alcohol<br />

also is an anes<strong>the</strong>tic, with PKCε being one<br />

<strong>of</strong> its many targets.<br />

“Our focus is brain chemistry. In our<br />

study, we have seen that PKCε and<br />

alcohol interacts and have pinpointed<br />

<strong>the</strong> binding side,” he said. “Now, we must<br />

determine <strong>the</strong> molecular mechanism <strong>of</strong><br />

<strong>the</strong> interaction. To do so, we are looking<br />

at how those two interact in <strong>the</strong> neuronal<br />

cells, which are <strong>the</strong> impulse-conducting<br />

cells in <strong>the</strong> brain.”<br />

The next steps for <strong>the</strong> group, which<br />

includes postdoctoral fellow Satyabrata<br />

Pany and UH undergraduate student<br />

Khoi Ly, will be to progress to animal<br />

trials with <strong>the</strong> mouse model and <strong>the</strong>n<br />

ultimately to clinical trials with humans.<br />

Graduate Students Earn International, National Travel Awards<br />

Two UH <strong>College</strong> <strong>of</strong> <strong>Pharmacy</strong> graduate students recently earned<br />

travel awards to international and national meetings, where<br />

<strong>the</strong>y delivered oral presentations on <strong>the</strong>ir research findings in<br />

collaboration with UHCOP faculty members.<br />

<strong>Pharmacy</strong> Administration doctoral student<br />

Mo Yang, who received her M.S. in <strong>Pharmacy</strong><br />

Administration in August, was selected to<br />

deliver an oral presentation <strong>of</strong> her work<br />

with Associate Pr<strong>of</strong>essor Amalia M. Issa,<br />

Ph.D., M.P.H., at <strong>the</strong> International Society<br />

for Pharmacoepidemiology’s 26th Annual<br />

Conference on Pharmacoepidemiology and<br />

Therapeutic Risk Management Aug. 19-22 in<br />

Brighton, U.K.<br />

Yang<br />

The presentation abstract, entitled “Assessment <strong>of</strong> <strong>the</strong> costeffectiveness<br />

<strong>of</strong> pharmacogenomic diagnostics for breast cancer,”<br />

will be published in a 2010 issue <strong>of</strong> Pharmacoepidemiology<br />

& Drug Safety. Yang and Issa conducted an evaluation and<br />

comparison <strong>of</strong> <strong>the</strong> cost-effectiveness <strong>of</strong> two commercially<br />

available gene expression-pr<strong>of</strong>iling tests – OncotypeDx<br />

and MammaPrint – used to predict <strong>the</strong> likelihood <strong>of</strong> breast<br />

cancer recurrence and guide adjuvant treatment decisions to<br />

potentially spare patients at low risk for recurrence <strong>the</strong> toxicity<br />

and morbidity <strong>of</strong> chemo<strong>the</strong>rapy. Their analysis concluded that<br />

MammaPrint is more cost-effective than OncotypeDx.<br />

Pharmacology graduate student Odelia<br />

Bongmba was selected to deliver an oral<br />

presentation <strong>of</strong> her work with Assistant<br />

Pr<strong>of</strong>essor MariVi Tejada-Simon, Ph.D.,<br />

M.Ed. (’07), at <strong>the</strong> Society for Advancement<br />

<strong>of</strong> Chicanos and Native Americans in Science<br />

meeting Sept. 30-Oct. 3 in Anaheim, Calif.<br />

Bongmba’s travel award from <strong>the</strong> Federation <strong>of</strong> Tucker<br />

American Societies for Experimental Biology is<br />

supported by <strong>the</strong> Minority Access to Research Careers Program,<br />

a National Institute <strong>of</strong> General Medical Sciences initiative.<br />

Her presentation abstract, entitled “Inactivation <strong>of</strong> <strong>the</strong> rac1<br />

gene affects <strong>the</strong> formation <strong>of</strong> dendritic spines,” revealed that<br />

suppression <strong>of</strong> rac1 gene in mice alters <strong>the</strong> normal morphology <strong>of</strong><br />

neuronal connections. The results suggest that Rac1 also might<br />

be responsible for <strong>the</strong> distorted connectivity observed in mental<br />

retardation and o<strong>the</strong>r neurological disorders affecting learning.<br />

<strong>University</strong> <strong>of</strong> <strong>Houston</strong> <strong>College</strong> <strong>of</strong> <strong>Pharmacy</strong> 13

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