B-type natriuretic peptide is neither itch-specific nor functions upstream of the GRP-GRPR signaling pathway

Molecular Pain

Zhou-Feng Chen²  Zhong-Qiu Zhao¹  Hui Li¹  Devin M Barry¹  Fu-Quan Huo¹  Li Wan¹  Xian-Yu Liu¹ 

[1] Departments of Anesthesiology, Washington University School of Medicine Pain Center, St. Louis, MO 63110, USA;Departments of Developmental Biology, Washington University School of Medicine Pain Center, St. Louis, MO 63110, USA

关键词: DRG;    Spinal cord;    Pain;    Itch;    GRPR;    GRP;    NPRA;    BNP;   

Others  :  861950
DOI  :  10.1186/1744-8069-10-4

 received in 2013-12-31, accepted in 2014-01-16,  发布年份 2014

【 摘 要 】

Background

A recent study by Mishra and Hoon identified B-type natriuretic peptide (BNP) as an important peptide for itch transmission and proposed that BNP activates spinal natriuretic peptide receptor-A (NPRA) expressing neurons, which release gastrin releasing peptide (GRP) to activate GRP receptor (GRPR) expressing neurons to relay itch information from the periphery to the brain (Science 340:968–971, 2013). A central premise for the validity of this novel pathway is the absence of GRP in the dorsal root ganglion (DRG) neurons. To this end, they showed that Grp mRNA in DRG neurons is either absent or barely detectable and claimed that BNP but not GRP is a major neurotransmitter for itch in pruriceptors. They showed that NPRA immunostaining is perfectly co-localized with Grp-eGFP in the spinal cord, and a few acute pain behaviors in Nppb^-/- mice were tested. They claimed that BNP is an itch-selective peptide that acts as the first station of a dedicated neuronal pathway comprising a GRP-GRPR cascade for itch. However, our studies, along with the others, do not support their claims.

Findings

We were unable to reproduce the immunostaining of BNP and NPRA as shown by Mishra and Hoon. By contrast, we were able to detect Grp mRNA in DRGs using in situ hybridization and real time RT-PCR. We show that the expression pattern of Grp mRNA is comparable to that of GRP protein in DRGs. Pharmacological and genetic blockade of GRP-GRPR signaling does not significantly affect intrathecal BNP-induced scratching behavior. We show that BNP inhibits inflammatory pain and morphine analgesia.

Conclusions

Accumulating evidence demonstrates that GRP is a key neurotransmitter in pruriceptors for mediating histamine-independent itch. BNP-NPRA signaling is involved in both itch and pain and does not function upstream of the GRP-GRPR dedicated neuronal pathway. The site of BNP action in itch and pain and its relationship with GRP remain to be clarified.

【 授权许可】

   
2014 Liu et al.; licensee BioMed Central Ltd.

【 图 表 】

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