Evaluation of age-based local anaesthetic dosing of bupivacaine for popliteal sciatic nerve block in children undergoing foot and ankle surgery: A prospective single arm interventional study. [PDF]
Parthasarathy S +2 more
europepmc +1 more source
Combined sciatic-psoas compartment nerve block in a patient with multiple myeloma
Orhan Binici, Fethi Akyol
openalex +1 more source
Sciatic nerve injury led to a significant increase in the expression of GPR35 in the ACC region of mice. This increased interaction with Nr4a1 can activate the PI3K/AKT signaling pathway, thereby reducing neuroinflammation and playing a role in alleviating hyperalgesia and depressive behavior in mice. ACC, anterior cingulate cortex.
Jianling Xu +9 more
wiley +1 more source
Simulated-based training for ultrasound-guided popliteal sciatic nerve block: determining the learning curve and transference to real patient. [PDF]
Miranda PF +6 more
europepmc +1 more source
Evaluation of a constant rate intravenous infusion of dexmedetomidine on the duration of a femoral and sciatic nerve block using lidocaine in dogs. [PDF]
Stabile M +5 more
europepmc +1 more source
Through network pharmacology, molecular docking, molecular dynamics simulations, and bioinformatics techniques, three potential core targets of EB for the treatment of pain‐depression comorbidity (EGFR, PTGS2, and JUN) were identified. Subsequent animal studies demonstrated that EB alleviates pain and depression‐like behaviors by inhibiting glial cell ...
Xuesong Yang +4 more
wiley +1 more source
Popliteal sciatic nerve block for high-risk patients undergoing lower limb angioplasty: A prospective double-blinded randomized controlled trial. [PDF]
Noikham A +5 more
europepmc +1 more source
Posterior approach to the lumbar plexus combined with a sciatic nerve block using lidocaine [PDF]
Juliana Farny +2 more
openalex +1 more source
Evaluating FABP5 as a Therapeutic Target for Pain Management
ABSTRACT Background and Objective Fatty acid‐binding proteins (FABPs) are intracellular lipid transporters. Pharmacological inhibition of FABP5 is analgesic in preclinical visceral, inflammatory, neuropathic and joint pain models. Genetic knockout or knockdown of FABP5 induces analgesia in select visceral and inflammatory pain models.
William Warren +4 more
wiley +1 more source

