Pawar Namrata, Dudhabhate Biru B, Borade Vaishnavi, Sahare Dipak K, Bhute Yogesh V, Subhedar Nishikant K, Kokare Dadasaheb M, Sakharkar Amul J
Department of Biotechnology, Savitribai Phule Pune University, Pune, 411 007, India.
Department of Pharmaceutical Sciences, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur, 440 033, India.
Mol Neurobiol. 2025 Feb;62(2):1388-1403. doi: 10.1007/s12035-024-04338-7. Epub 2024 Jul 10.
Neuropeptide cocaine- and amphetamine-regulated transcript peptide (CARTp) is known to play an important role in reward processing. The rats conditioned to intra-cranial self-stimulation (ICSS) showed massive upregulation of CART protein and mRNA in the vicinity of the electrode implanted to deliver the electric current directly at the lateral hypothalamus (LH)-medial forebrain bundle (MFB) area. However, the underlying mechanisms leading to the upregulation of CART in ICSS animals remain elusive. We tested the putative role of CREB-binding protein (CBP), an epigenetic enzyme with intrinsic histone acetyltransferase (HAT) activity, in regulating CART expression during ICSS. An electrode was implanted in LH-MFB and the rats were conditioned to self-stimulation in an operant chamber. CBP siRNA was delivered ipsilaterally in the LH-MFB to knock-down CBP and the effects on lever press activity were monitored. While ICSS-conditioned rats showed distinct increase in CART, CBP and pCREB levels, enhanced CBP binding and histone acetylation (H3K9ac) were noticed on the CART promoter in chromatin immunoprecipitation assay. Direct infusion of CBP siRNA in the LH-MFB lowered lever press activity, CBP levels, histone acetylation at the CART promoter, and CART mRNA and peptide expression. Co-infusion of CARTp in LH-MFB rescued the waning effects of CBP siRNA on self-stimulation. We suggest that CBP-mediated histone acetylation may play a causal role in CART expression in LH, which in turn may drive the positive reinforcement of lever press activity.
已知神经肽可卡因和苯丙胺调节转录肽(CARTp)在奖赏处理中发挥重要作用。经颅内自我刺激(ICSS)训练的大鼠在植入电极以直接在下丘脑外侧(LH)-内侧前脑束(MFB)区域传递电流的电极附近,CART蛋白和mRNA大量上调。然而,导致ICSS动物中CART上调的潜在机制仍不清楚。我们测试了CREB结合蛋白(CBP),一种具有内在组蛋白乙酰转移酶(HAT)活性的表观遗传酶,在ICSS期间调节CART表达中的假定作用。将电极植入LH-MFB,大鼠在操作性条件反射箱中接受自我刺激训练。将CBP小干扰RNA(siRNA)同侧注入LH-MFB以敲低CBP,并监测其对杠杆按压活动的影响。虽然经ICSS训练的大鼠CART、CBP和磷酸化CREB(pCREB)水平明显增加,但在染色质免疫沉淀试验中,在CART启动子上观察到CBP结合增强和组蛋白乙酰化(H3K9ac)。在LH-MFB中直接注入CBP siRNA降低了杠杆按压活动、CBP水平、CART启动子处的组蛋白乙酰化以及CART mRNA和肽的表达。在LH-MFB中共同注入CARTp挽救了CBP siRNA对自我刺激的减弱作用。我们认为,CBP介导的组蛋白乙酰化可能在LH中CART的表达中起因果作用,这反过来可能驱动杠杆按压活动的正性强化。