The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Voluntary exercise increases axonal regeneration from sensory neurons
Open accessAbstract
Recent advances in understanding the role of neurotrophins on activity-dependent plasticity have provided insight into how behavior can affect specific aspects of neuronal biology. We present evidence that voluntary exercise can prime adult dorsal root ganglion neurons for increased axonal regeneration through a neurotrophin-dependent mechanism. Dorsal root ganglion neurons showed an increase in neurite outgrowth when cultured from animals that had undergone 3 or 7 days of exercise compared with sedentary animals. Neurite length over 18–22 h in culture correlated directly with the distance that animals ran. The exercise-conditioned animals also showed enhanced regrowth of axons after an in vivo nerve crush injury. Sensory ganglia from the 3- and 7-day-exercised animals contained higher brain-derived neurotrophic factor, neurotrophin 3, synapsin I, and GAP43 mRNA levels than those from sedentary animals. Consistent with the rise in brain-derived neurotrophic factor and neurotrophin 3 during exercise, the increased growth potential of the exercise-conditioned animals required activation of the neurotrophin signaling in vivo during the exercise period but did not require new mRNA synthesis in culture.
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Cites
Synaptic Activity and the Construction of Cortical Circuits
Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048
NEUROTROPHINS AND SYNAPTIC PLASTICITY
McAllister, A. K., Katz, L. C., & Lo, D. C. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.295 · Cited by 1,337
Vaynman, S., Ying, Z., & Gomez-Pinilla, F. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.08.001 · Cited by 396
Self-citationActivity-dependent synaptogenesis in the adult Mammalian cortex
Zito, K., & Svoboda, K. (2002) · Neuron · doi:10.1016/s0896-6273(02)00903-0 · Cited by 134
Cited by
The Influence of Exercise on Cognitive Abilities
Gomez‐Pinilla, F., & Hillman, C. (2013) · Comprehensive Physiology · doi:10.1002/cphy.c110063 · Cited by 599
Voss, M. W., Heo, S., Prakash, R. S., Erickson, K. I., Alves, H., Chaddock, L., Szabo, A. N., Mailey, E. L., Wójcicki, T. R., White, S. M., et al. (2013) · Human Brain Mapping · doi:10.1002/hbm.22119 · Cited by 553
Rojas Vega, S., Strüder, H. K., Vera Wahrmann, B., Schmidt, A., Bloch, W., & Hollmann, W. (2006) · Brain Research · doi:10.1016/j.brainres.2006.08.105 · Cited by 357
Ballermann, M., & Fouad, K. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04726.x · Cited by 279
Emerging Relationships between Exercise, Sensory Nerves, and Neuropathic Pain
Cooper, M. A., Kluding, P. M., & Wright, D. E. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00372 · Cited by 105
Metadata
- Authors
- Molteni, R., Zheng, J.-Q., Ying, Z., Gómez-Pinilla, F., & Twiss, J. L.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2004-05-24
- Volume
- 101
- Issue
- 22
- Pages
- 8473-8478
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2118663281
- Cited by
- 210
- References
- 4
- FWCI
- 2.30
- Type
- journal article
- Language
- en
- Open access
- green
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