G
Galo L. Mejia
Researcher at University of Texas at Dallas
Publications - 23
Citations - 574
Galo L. Mejia is an academic researcher from University of Texas at Dallas. The author has contributed to research in topics: Neuropathic pain & AMPK. The author has an hindex of 12, co-authored 21 publications receiving 377 citations. Previous affiliations of Galo L. Mejia include University of Arizona.
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Journal ArticleDOI
Sigma 2 Receptor/Tmem97 Agonists Produce Long Lasting Antineuropathic Pain Effects in Mice
TL;DR: It is shown that the TMEM97 gene is expressed in mouse and human dorsal root ganglion including populations of neurons that are involved in pain; however, the gene is also likely expressed in non-neuronal cells that may contribute to the observed behavioral effects.
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Mycobacterium tuberculosis Sulfolipid-1 Activates Nociceptive Neurons and Induces Cough
Cody R. Ruhl,Breanna L. Pasko,Haaris S. Khan,Lexy M. Kindt,Chelsea E. Stamm,Luis H. Franco,Connie C.W. Hsia,Min Zhou,Colton R. Davis,Tian Qin,Laurent Gautron,Michael D. Burton,Galo L. Mejia,Dhananjay K. Naik,Gregory Dussor,Theodore J. Price,Michael U. Shiloh +16 more
TL;DR: It is shown that an Mtb organic extract activates nociceptive neurons in vitro and the Mtb glycolipid sulfolipid-1 (SL-1) as the nocICEptive molecule and Mtb-infected guinea pigs cough in a manner dependent on SL-1 synthesis.
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Spinal Dopaminergic Projections Control the Transition to Pathological Pain Plasticity via a D1/D5-Mediated Mechanism
Ji Young Kim,Dipti V. Tillu,Tammie Quinn,Galo L. Mejia,Adia Shy,Marina N. Asiedu,Elaine Murad,Alan P. Schumann,Stacie K. Totsch,Robert E. Sorge,Patrick W. Mantyh,Gregory Dussor,Theodore J. Price +12 more
TL;DR: A novel role for descending dopaminergic neurons in the maintenance of pathological pain plasticity is demonstrated, consistent with reconsolidation-like effects in the spinal dorsal horn.
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Neuropathic Pain Creates an Enduring Prefrontal Cortex Dysfunction Corrected by the Type II Diabetic Drug Metformin But Not by Gabapentin.
Stephanie Shiers,Grishma Pradhan,Juliet Mwirigi,Galo L. Mejia,Ayesha Ahmad,Sven Kroener,Theodore J. Price +6 more
TL;DR: A neuropathic pain model in mice is used to demonstrate that male (but not female) mice show a robust pain-related deficit in attentional set-shifting, which is associated with structural plasticity in axon initial segments in the infralimbic cortex.
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Spinal Inhibition of P2XR or p38 Signaling Disrupts Hyperalgesic Priming in Male, but not Female, Mice.
TL;DR: This work is consistent with previous findings that P2XR and p38 inhibition can lead to male-specific effects on pain behaviors in mice, however, given that microglial activation at time points where these drugs were effective, it is questioned whether these effects can be completely attributed to microglia.