Improvement of diabetes-induced spinal cord axon injury with taurine via nerve growth factor-dependent Akt/mTOR pathway

• Published in: Amino acids Vol. 56; no. 1; p. 32
• Main Authors: Wang, Yachen, Gao, Bihu, Chen, Xiaochi, Shi, Xiaoxia, Li, Shuangyue, Zhang, Qing, Zhang, Cong, Piao, Fengyuan
• Format: Journal Article
• Language: English
• Published: Vienna Springer Vienna 18.04.2024; Springer Nature B.V
• Subjects: AKT protein; Analytical Chemistry; Antibodies; Axonogenesis; Biochemical Engineering; Biochemistry; Biomedical and Life Sciences; Cerebral cortex; Degeneration; Diabetes; Diabetes mellitus; Diabetic neuropathy; GAP-43 protein; Growth factors; Life Sciences; Nerve growth factor; Nerves; Neurobiology; Neurodegeneration; Neurological complications; Neurons; Neuroprotection; Original Article; Peripheral neuropathy; Phosphorylation; Proteomics; Spinal cord; Spinal cord injuries; Streptozocin; Taurine; TOR protein; TrkA protein; TrkA receptors; Taurine; Diabetic neuropathy; Nerve growth factor; Diabetes mellitus; Spinal cord axon injury
• ISSN: 1438-2199; 0939-4451; 1438-2199
• DOI: 10.1007/s00726-024-03392-8

Diabetic neuropathy (DN) is a common neurological complication caused by diabetes mellitus (DM). Axonal degeneration is generally accepted to be the major pathological change in peripheral DN. Taurine has been evidenced to be neuroprotective in various aspects, but its effect on spinal cord axon injury (SCAI) in DN remains barely reported. This study showed that taurine significantly ameliorated axonal damage of spinal cord (SC), based on morphological and functional analyses, in a rat model of DN induced by streptozotocin (STZ). Taurine was also found to induce neurite outgrowth in cultured cerebral cortex neurons with high glucose exposure. Moreover, taurine up-regulated the expression of nerve growth factor (NGF) and neurite outgrowth relative protein GAP-43 in rat DN model and cultured cortical neurons/VSC4.1 cells. Besides, taurine increased the activating phosphorylation signals of TrkA, Akt, and mTOR. Mechanistically, the neuroprotection by taurine was related to the NGF–pAKT–mTOR axis, because either NGF-neutralizing antibody or Akt or mTOR inhibitors was found to attenuate its beneficial effects. Together, our results demonstrated that taurine promotes spinal cord axon repair in a model of SCAI in STZ-induced diabetic rats, mechanistically associating with the NGF-dependent activation of Akt/mTOR pathway.