Skip to main content

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 860))

Abstract

The carotid body is a multi-modal sensor and it has been debated if it senses low glucose. We have hypothesized that the carotid body is modified by some metabolic factors other than glucose and contributes to whole body glucose metabolism. This study examined the roles of insulin, leptin and transient receptor potential (TRP) channels on carotid sinus nerve (CSN) chemoreceptor discharge. In agreement with other studies, CSN activity was not modified by low glucose. Insulin did not affect the CSN hypoxic response. Leptin significantly augmented the CSN response to hypoxia and nonspecific Trp channel blockers (SKF96365, 2-APB) reversed the effect of leptin. Gene expression analysis showed high expression of Trpm3, 6, and 7 channels in the carotid body and petrosal ganglion. The results suggest that the adult mouse carotid body does not sense glucose levels directly. The carotid body may contribute to neural control of glucose metabolism via leptin receptor-mediated TRP channel activation.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 109.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Alvarez-Buylla R, Alvarez-Buylla ER (1988) Carotid sinus receptors participate in glucose homeostasis. Respir Physiol 72:347–360

    Article  PubMed  CAS  Google Scholar 

  • Balbir A, Lee H, Okumura M, Biswal S, Fitzgerald RS, Shirahata M (2007) A search for genes that may confer divergent morphology and function in the carotid body between two strains of mice. Am J Physiol Lung Cell Mol Physiol 292:L704–L715

    Article  PubMed  CAS  Google Scholar 

  • Bin-Jaliah I, Maskell PD, Kumar P (2004) Indirect sensing of insulin-induced hypoglycaemia by the carotid body in the rat. J Physiol 556:255–266

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Conde SV, Obeso A, Gonzalez C (2007) Low glucose effects on rat carotid body chemoreceptor cells’ secretory responses and action potential frequency in the carotid sinus nerve. J Physiol 585:721–730

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Gallego-Martin T, Fernandez-Martinez S, Rigual R, Obeso A, Gonzalez C (2012) Effects of low glucose on carotid body chemoreceptor cell activity studied in cultures of intact organs and in dissociated cells. Am J Physiol Cell Physiol 302:C1128–C1140

    Article  PubMed  CAS  Google Scholar 

  • Gonzalez C, Almaraz L, Obeso A, Rigual R (1994) Carotid body chemoreceptors: from natural stimuli to sensory discharges. Physiol Rev 74:829–898

    PubMed  CAS  Google Scholar 

  • Koyama Y, Coker RH, Stone EE, Lacy DB, Jabbour K, Williams PE, Wasserman DH (2000) Evidence that carotid bodies play an important role in glucoregulation in vivo. Diabetes 49:1434–1442

    Article  PubMed  CAS  Google Scholar 

  • Pardal R, López-Barneo J (2002) Low glucose-sensing cells in the carotid body. Nat Neurosci 5:197–198

    Article  PubMed  CAS  Google Scholar 

  • Porzionato A, Rucinski A, Macchi V, Stecco C, Castagliuoloc I, Malendowicz LK, De Caro R (2011) Expression of leptin and leptin receptor isoforms in the rat and human carotid body. Brain Res 1385:56–67

    Article  PubMed  CAS  Google Scholar 

  • Qiu J, Fang Y, Rønnekleiv OK, Kelly MJ (2010) Leptin excites POMC neurons via activation of TRPC channels. J Neurosci 30:1560–1565

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Shin MK, Yao Q, Jun JC, Bevans-Fonti S, Yoo DY, Han W, Mesarwi O, Richardson R, Fu YY, Pasricha PJ, Schwartz AR, Shirahata M, Polotsky VY (2014) Carotid body denervation prevents fasting hyperglycemia during chronic intermittent hypoxia. J Appl Physiol 117:765–776

    Article  PubMed  CAS  Google Scholar 

  • Tankersley CG, Tang W-Y, Wang X, Pardo C, Bierman A, Shirahata M (2013) Effect of leptin on hypoxic ventilator regulation. ATS international conference A5763

    Google Scholar 

  • Wehrwein EA, Basu R, Basu A, Curry TB, Rizza RA, Joyner MJ (2010) Hyperoxia blunts counterregulation during hypoglycaemia in humans: possible role for the carotid bodies? J Physiol 588:4593–4601

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Zhang M, Buttigieg J, Nurse CA (2007) Neurotransmitter mechanisms mediating low-glucose signalling in cocultures and fresh tissue slices of rat carotid body. J Physiol 578:735–750

    Article  PubMed  CAS  PubMed Central  Google Scholar 

Download references

Acknowledgements

This work was funded, in part, by HL081345, ES016817, HL080105, and AHA 12POST118200001.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Shirahata .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2015 Springer International Publishing Switzerland

About this chapter

Cite this chapter

Shirahata, M., Tang, WY., Shin, MK., Polotsky, V.Y. (2015). Is the Carotid Body a Metabolic Monitor?. In: Peers, C., Kumar, P., Wyatt, C., Gauda, E., Nurse, C., Prabhakar, N. (eds) Arterial Chemoreceptors in Physiology and Pathophysiology. Advances in Experimental Medicine and Biology, vol 860. Springer, Cham. https://doi.org/10.1007/978-3-319-18440-1_17

Download citation

Publish with us

Policies and ethics