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Oxytocin-Dependent Regulation of TRPs Expression in Trigeminal Ganglion Neurons Attenuates Orofacial Neuropathic Pain following Infraorbital Nerve Injury in Rats
by
Hitomi, Suzuro
, Iwata, Koichi
, Yonehara, Yoshiyuki
, Noma, Noboru
, Matsui, Tomoyuki
, Furukawa, Akihiko
, Okubo, Masakazu
, Ando, Masatoshi
, Hayashi, Yoshinori
, Oto, Tatsuki
, Inada, Takanobu
, Shibuta, Ikuko
, Shinoda, Masamichi
, Kaneko, Tadayoshi
, Fukaya, Chikashi
in
Animals
/ Cranial Nerve Injuries - complications
/ Disease Models, Animal
/ Facial Neuralgia - diagnosis
/ Facial Neuralgia - etiology
/ Facial Neuralgia - metabolism
/ Fluorescent Antibody Technique
/ Gene Expression Regulation - drug effects
/ Neurons - metabolism
/ Oxytocin - administration & dosage
/ Pain Threshold - drug effects
/ Rats
/ Receptors, Oxytocin - genetics
/ Receptors, Oxytocin - metabolism
/ Transient Receptor Potential Channels - genetics
/ Transient Receptor Potential Channels - metabolism
/ Trigeminal Ganglion - metabolism
2020
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Oxytocin-Dependent Regulation of TRPs Expression in Trigeminal Ganglion Neurons Attenuates Orofacial Neuropathic Pain following Infraorbital Nerve Injury in Rats
by
Hitomi, Suzuro
, Iwata, Koichi
, Yonehara, Yoshiyuki
, Noma, Noboru
, Matsui, Tomoyuki
, Furukawa, Akihiko
, Okubo, Masakazu
, Ando, Masatoshi
, Hayashi, Yoshinori
, Oto, Tatsuki
, Inada, Takanobu
, Shibuta, Ikuko
, Shinoda, Masamichi
, Kaneko, Tadayoshi
, Fukaya, Chikashi
in
Animals
/ Cranial Nerve Injuries - complications
/ Disease Models, Animal
/ Facial Neuralgia - diagnosis
/ Facial Neuralgia - etiology
/ Facial Neuralgia - metabolism
/ Fluorescent Antibody Technique
/ Gene Expression Regulation - drug effects
/ Neurons - metabolism
/ Oxytocin - administration & dosage
/ Pain Threshold - drug effects
/ Rats
/ Receptors, Oxytocin - genetics
/ Receptors, Oxytocin - metabolism
/ Transient Receptor Potential Channels - genetics
/ Transient Receptor Potential Channels - metabolism
/ Trigeminal Ganglion - metabolism
2020
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Oxytocin-Dependent Regulation of TRPs Expression in Trigeminal Ganglion Neurons Attenuates Orofacial Neuropathic Pain following Infraorbital Nerve Injury in Rats
by
Hitomi, Suzuro
, Iwata, Koichi
, Yonehara, Yoshiyuki
, Noma, Noboru
, Matsui, Tomoyuki
, Furukawa, Akihiko
, Okubo, Masakazu
, Ando, Masatoshi
, Hayashi, Yoshinori
, Oto, Tatsuki
, Inada, Takanobu
, Shibuta, Ikuko
, Shinoda, Masamichi
, Kaneko, Tadayoshi
, Fukaya, Chikashi
in
Animals
/ Cranial Nerve Injuries - complications
/ Disease Models, Animal
/ Facial Neuralgia - diagnosis
/ Facial Neuralgia - etiology
/ Facial Neuralgia - metabolism
/ Fluorescent Antibody Technique
/ Gene Expression Regulation - drug effects
/ Neurons - metabolism
/ Oxytocin - administration & dosage
/ Pain Threshold - drug effects
/ Rats
/ Receptors, Oxytocin - genetics
/ Receptors, Oxytocin - metabolism
/ Transient Receptor Potential Channels - genetics
/ Transient Receptor Potential Channels - metabolism
/ Trigeminal Ganglion - metabolism
2020
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Oxytocin-Dependent Regulation of TRPs Expression in Trigeminal Ganglion Neurons Attenuates Orofacial Neuropathic Pain following Infraorbital Nerve Injury in Rats
Journal Article
Oxytocin-Dependent Regulation of TRPs Expression in Trigeminal Ganglion Neurons Attenuates Orofacial Neuropathic Pain following Infraorbital Nerve Injury in Rats
2020
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Overview
We evaluated the mechanisms underlying the oxytocin (OXT)-induced analgesic effect on orofacial neuropathic pain following infraorbital nerve injury (IONI). IONI was established through tight ligation of one-third of the infraorbital nerve thickness. Subsequently, the head withdrawal threshold for mechanical stimulation (MHWT) of the whisker pad skin was measured using a von Frey filament. Trigeminal ganglion (TG) neurons innervating the whisker pad skin were identified using a retrograde labeling technique. OXT receptor-immunoreactive (IR), transient receptor potential vanilloid 1 (TRPV1)-IR, and TRPV4-IR TG neurons innervating the whisker pad skin were examined on post-IONI day 5. The MHWT remarkably decreased from post-IONI day 1 onward. OXT application to the nerve-injured site attenuated the decrease in MHWT from day 5 onward. TRPV1 or TRPV4 antagonism significantly suppressed the decrement of MHWT following IONI. OXT receptors were expressed in the uninjured and Fluoro-Gold (FG)-labeled TG neurons. Furthermore, there was an increase in the number of FG-labeled TRPV1-IR and TRPV4-IR TG neurons, which was inhibited by administering OXT. This inhibition was suppressed by co-administration with an OXT receptor antagonist. These findings suggest that OXT application inhibits the increase in TRPV1-IR and TRPV4-IR TG neurons innervating the whisker pad skin, which attenuates post-IONI orofacial mechanical allodynia.
Publisher
MDPI
Subject
/ Cranial Nerve Injuries - complications
/ Facial Neuralgia - diagnosis
/ Facial Neuralgia - metabolism
/ Fluorescent Antibody Technique
/ Gene Expression Regulation - drug effects
/ Oxytocin - administration & dosage
/ Pain Threshold - drug effects
/ Rats
/ Receptors, Oxytocin - genetics
/ Receptors, Oxytocin - metabolism
/ Transient Receptor Potential Channels - genetics
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