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. 2020 Mar 20;57(6):2521–2538. doi: 10.1007/s12035-020-01900-x

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — Knockdown of CaMKKβ reduces AMPK phosphorylation. a–c Immunoblots showing the relative expression of a CaMKKβ, b pAMPK (on Thr-172), and c CaMKKα in control (scrambled siRNA) and CaMKKβ siRNA–transfected cultured adult rat primary DRG neurons (GAPDH used as a loading control in a and c from normal rats). Adult rat DRGs were freshly dissected, dissociated, and transfected with siRNAs using Amaxa nucleofection reagent and cultured in defined media for 48 h. The total proteins were separated by SDS-PAGE and immunoblotted