Skip to main content

R-type Calcium Channel Isoform in Rat Dorsal Root Ganglion Neurons.

Publication ,  Journal Article
Fang, Z; Hwang, JH; Kim, JS; Jung, SJ; Oh, SB
Published in: The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology
February 2010

R-type Ca(v)2.3 high voltage-activated Ca(2+) channels in peripheral sensory neurons contribute to pain transmission. Recently we have demonstrated that, among the six Ca(v)2.3 isoforms (Ca(v)2.3a~Ca(v)2.3e), the Ca(v)2.3e isoform is primarily expressed in trigeminal ganglion (TG) nociceptive neurons. In the present study, we further investigated expression patterns of Ca(v)2.3 isoforms in the dorsal root ganglion (DRG) neurons. As in TG neurons, whole tissue RT-PCR analyses revealed the presence of two isoforms, Ca(v)2.3a and Ca(v)2.3e, in DRG neurons. Single-cell RT-PCR detected the expression of Ca(v)2.3e mRNA in 20% (n=14/70) of DRG neurons, relative to Ca(v)2.3a expression in 2.8% (n=2/70) of DRG neurons. Ca(v)2.3e mRNA was mainly detected in small-sized neurons (n=12/14), but in only a few medium-sized neurons (n=2/14) and not in large-sized neurons, indicating the prominence of Ca(v)2.3e in nociceptive DRG neurons. Moreover, Ca(v)2.3e was preferentially expressed in tyrosine-kinase A (trkA)-positive, isolectin B4 (IB4)-negative and transient receptor potential vanilloid 1 (TRPV1)-positive neurons. These results suggest that Ca(v)2.3e may be the main R-type Ca(2+) channel isoform in nociceptive DRG neurons and thereby a potential target for pain treatment, not only in the trigeminal system but also in the spinal system.

Duke Scholars

Published In

The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology

DOI

EISSN

2093-3827

ISSN

1226-4512

Publication Date

February 2010

Volume

14

Issue

1

Start / End Page

45 / 49

Related Subject Headings

  • Pharmacology & Pharmacy
  • 3214 Pharmacology and pharmaceutical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences
  • 0606 Physiology
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Fang, Z., Hwang, J. H., Kim, J. S., Jung, S. J., & Oh, S. B. (2010). R-type Calcium Channel Isoform in Rat Dorsal Root Ganglion Neurons. The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology, 14(1), 45–49. https://doi.org/10.4196/kjpp.2010.14.1.45
Fang, Zhi, Jae Hong Hwang, Joong Soo Kim, Sung Jun Jung, and Seog Bae Oh. “R-type Calcium Channel Isoform in Rat Dorsal Root Ganglion Neurons.The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology 14, no. 1 (February 2010): 45–49. https://doi.org/10.4196/kjpp.2010.14.1.45.
Fang Z, Hwang JH, Kim JS, Jung SJ, Oh SB. R-type Calcium Channel Isoform in Rat Dorsal Root Ganglion Neurons. The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology. 2010 Feb;14(1):45–9.
Fang, Zhi, et al. “R-type Calcium Channel Isoform in Rat Dorsal Root Ganglion Neurons.The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology, vol. 14, no. 1, Feb. 2010, pp. 45–49. Epmc, doi:10.4196/kjpp.2010.14.1.45.
Fang Z, Hwang JH, Kim JS, Jung SJ, Oh SB. R-type Calcium Channel Isoform in Rat Dorsal Root Ganglion Neurons. The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology. 2010 Feb;14(1):45–49.

Published In

The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology

DOI

EISSN

2093-3827

ISSN

1226-4512

Publication Date

February 2010

Volume

14

Issue

1

Start / End Page

45 / 49

Related Subject Headings

  • Pharmacology & Pharmacy
  • 3214 Pharmacology and pharmaceutical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences
  • 0606 Physiology