I can recommend Bogomoletz Institute of Physiology in Kyiv, Ukraine.
Especially labs of prof. Oleg Krishtal (https://www.researchgate.net/profile/Oleg_Krishtal2), prof. Pavel Belan (https://www.researchgate.net/profile/Pavel_Belan), prof. Nana Voitenko (https://www.researchgate.net/profile/Nana_Voitenko). These labs works with DRG neurons (cultured and acute dissociated) and lab of prof. Voitenko also makes patch-clamp recordings from whole spinal cord. I think it is close to your task.
I have found somebody that might be able to help me with the training or to put me in contact with. I really appreciate your feedback and I will keep it in mind.
I have managed to record some TRPA1 current but my method does not seems to be optimal. I have not figure out how to do it in a reproducible manner, however Xu et al., 1997 PNAS managed to do so in intact DRG without the use of enzymes and without dissociation. The other paper that I have followed was Zhang et al., 1997, in this one , Authors do use some collagenase to break into it.
The goal is to practice the in vitro recording in "intact" DRG in order to move to in vivo DRG Ma et al., 2010.
I do agree satellite cells are an an issue but I am sure i will get over it.