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DNMT3a in the hippocampal CA1 is crucial in the acquisition of morphine selfâadministration in rats
Drugâreinforced excessive operant responding is one fundamental feature of long-lasting addictionâlike behaviors and relapse in animals. However, the transcriptional regulatory mechanisms responsible for the persistent drugâspecific (not natural rewards) operant behavior are not entirely clear. In this study, we demonstrate a key role for one of the de novo DNA methyltransferase, DNMT3a, in the acquisition of morphine selfâadministration (SA) in rats. The expression of DNMT3a in the hippocampal CA1 region but not in the nucleus accumbens shell was significantly upâregulated after 1â and 7âday morphine SA (0.3 mg/kg/infusion) but not after the yoked morphine injection. On the other hand, saccharin SA did not affect the expression of DNMT3a or DNMT3b. DNMT inhibitor 5âazaâ2âdeoxycytidine (5âaza) microinjected into the hippocampal CA1 significantly attenuated the acquisition of morphine SA. Knockdown of DNMT3a also impaired the ability to acquire the morphine SA. Overall, these findings suggest that DNMT3a in the hippocampus plays an important role in the acquisition of morphine SA and may be a valid target to prevent the development of morphine addiction.
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A comment on "Ab initio calculations of pressure-dependence of high-order elastic constants using finite deformations approach" by I. Mosyagin, A.V. Lugovskoy, O.M. Krasilnikov, Yu.Kh. Vekilov, S.I. Simak and I.A. Abrikosov
Recently, I. Mosyagin, A.V. Lugovskoy, O.M. Krasilnikov, Yu.Kh. Vekilov, S.I.
Simak and I.A. Abrikosov in the paper: "Ab initio calculations of
pressure-dependence of high-order elastic constants using finite deformations
approach"[Computer Physics Communications 220 (2017) 2030] presented a
description of a technique for ab initio calculations of the pressure
dependence of second- and third-order elastic constants. Unfortunately, the
work contains serious and fundamental flaws in the field of finite-deformation
solid mechanics.Comment: 3 pages, 0 figure
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