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CPDD 78th Annual Scientific Meeting Program

2016-78th-CPDD-Program-Book-6-07-16FINAL

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SYMPOSIA<br />

Tuesday, June 14<br />

VII.<br />

5HT2A and 5HT2C ligands as potential therapeutics for substance use<br />

disorders<br />

Chairs: Jane B. Acri and Leonard Howell<br />

We will present and discuss data relevant to the clinical advancement of 5HT2 ligands<br />

as substance use treatment medications. There are no approved medications for<br />

cocaine, methamphetamine, or THC use disorders, and these results may suggest<br />

clinical efficacy for substance use disorders. The 5HT system can influence the abuserelated<br />

effects of cocaine and other drugs of abuse through its direct and indirect<br />

interactions with dopaminergic systems in key brain areas. The regional distribution<br />

of 5HT2A and 5HT2C involve the prefrontal cortex, the nucleus accumbens and the<br />

ventral tegmental area. The two receptor systems can functionally oppose each other<br />

in terms of their regulation of the dopaminergic signaling. Several selective ligands<br />

have recently been developed by pharma for different indications; lorcaserin a 5HT2C<br />

agonist is in clinical use for weight reduction, and pimavanserin, a 5HT2A antagonist<br />

may soon be approved for the treatment of psychosis in Parkinson’s Disease. Clinical<br />

availability of selective ligands will greatly enhance our ability to translate these<br />

findings in human clinical trials. These compounds have recently been evaluated in<br />

drug self-administration models using non-human primates trained to self-administer<br />

cocaine, methamphetamine, or THC, using FR, PR, or choice models. These results will<br />

be presented and discussed in terms of relevance to the treatment of substance use<br />

disorders.<br />

VIII. Neonatal Abstinence Syndrome: Context and consequences in 2016<br />

Chairs: Karol Kaltenbach and Hendree Jones<br />

Under the banner of fetal protection, judges and prosecutors have implemented<br />

punitive approaches against women who use prescribed and non-prescribed opioids<br />

during pregnancy. Policy makers mirror such punitive approaches in laws passed that<br />

focus on women who use drugs while pregnant. The symposium will review the current<br />

situation for women who use substances during pregnancy and their NAS-diagnosed<br />

babies. These actions in the judicial-political sphere suggest that the science of NAS is<br />

well understood. While there are numerous reports in the empirical literature<br />

documenting efforts to assess and treat NAS over the past 50 years, rigorous studies<br />

testing the best ways to assess and treat these infants are relatively recent as are<br />

studies that identify factors that exacerbate or mitigate the severity of NAS. The state<br />

of the science in assessment; efficacy of medication used to treat NAS; and protocols<br />

for initiation of treatment and weaning will be described. Factors that have been<br />

recently been identified that exacerbate the severity and length of treatment as well as<br />

changes in hospital policies and practices that been shown to be effective in reducing<br />

NAS severity will be discussed. These presentations will outline how a diagnosis of<br />

NAS is not a diagnosis of maternal substance use disorder; an indication of a negative<br />

relationship between substance use and fetal outcome

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