The Effects of Diabetes and High-Fat Diet on Polymodal Nociceptor and Cold Thermoreceptor Nerve Terminal Endings in the Corneal Epithelium

Invest Ophthalmol Vis Sci. 2019 Jan 2;60(1):209-217. doi: 10.1167/iovs.18-25788.

Abstract

Purpose: There is a substantial body of evidence indicating that corneal sensory innervation is affected by pathology in a range of diseases. However, there are no published studies that have directly assessed whether the nerve fiber density of the different subpopulations of corneal sensory neurons are differentially affected. The present study explored the possibility that the intraepithelial nerve fiber density of corneal polymodal nociceptors and cold thermoreceptors are differentially affected in mice fed with a high-fat high cholesterol (HFHC; 21% fat, 2% cholesterol) diet and in those that also have diabetes.

Methods: The mice were fed the HFHC diet for the duration of the experiment (up to 40 weeks). Mice in the diabetes group had hyperglycaemia induced with streptozotocin after 15 weeks on the HFHC diet. Age-matched control animals were fed a standard diet. All corneal nerve fibers were labeled with a pan neuronal antibody (antiprotein gene product 9.5), and polymodal nociceptors and cold thermoreceptors were labeled with antibodies directed against transient receptor potential cation channel, subfamily V, member 1 and transient receptor potential cation channel subfamily M member 8, respectively.

Results: The mice fed a HFHC diet and those that in addition have hyperglycemia have similar reductions in corneal nerve fiber density consistent with small fiber neuropathy. Importantly, both treatments more markedly affected the intraepithelial axons of cold thermoreceptors than those of polymodal nociceptors.

Conclusions: The results provide evidence that distinct subpopulations of corneal sensory neurons can be differentially affected by pathology.

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Type 2 / complications*
  • Diet, High-Fat / adverse effects*
  • Epithelium, Corneal / innervation*
  • Hyperglycemia / etiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Fluorescence
  • Nerve Endings / physiology
  • Nerve Fibers / pathology
  • Nociceptors / metabolism*
  • Streptozocin
  • TRPM Cation Channels / metabolism
  • TRPV Cation Channels / metabolism
  • Thermoreceptors / metabolism*
  • Trigeminal Nerve / metabolism*
  • Trigeminal Nerve Diseases / etiology*
  • Trigeminal Nerve Diseases / metabolism

Substances

  • Blood Glucose
  • TRPM Cation Channels
  • TRPM8 protein, mouse
  • TRPV Cation Channels
  • TRPV1 protein, mouse
  • Streptozocin