Diabetes Metab J.  2018 Apr;42(2):169-172. 10.4093/dmj.2018.42.2.169.

Morphologic Comparison of Peripheral Nerves in Adipocyte Tissue from db/db Diabetic versus Normal Mice

Affiliations
  • 1Division of Endocrinology and Metabolism, Department of Internal Medicine, Chonbuk National University Medical School, Research Institute of Clinical Medicine of Chonbuk National University-Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, Korea. mdjinhy@jbnu.ac.kr

Abstract

Present study investigated the morphologic changes of autonomic nerves in the adipose tissue in diabetic animal model. Male obese type 2 diabetic db/db mice and age matched non-diabetic db/m control mice were used. Epididymal adipose tissue from diabetic db/db mice with that from control heterozygous db/m mice was compared using confocal microscopy-based method to visualize intact whole adipose tissue. Immunohistochemistry with tyrosine hydroxylase for sympathetic (SP), choline acetyltransferase for parasympathetic (PSP), and protein gene product 9.5 (PGP 9.5) for whole autonomic nerves was performed. The quantity of immunostained portion of SP, PSP, and PGP 9.5 stained nerve fibers showed decreased trend in diabetic group; however, the ratio of SP/PSP of adipose tissue was higher in diabetic group compared with control group as follows (0.70±0.30 vs. 0.95±0.25, P < 0.05; normal vs. diabetic, respectively). Both SP and PSP nerve fibers were observed in white adipose tissue and PSP nerve fibers were suggested as more decreased in diabetes based on our observation.

Keyword

Adipose tissue; Diabetes mellitus; Neuropathy; Peripheral nerves

MeSH Terms

Adipocytes*
Adipose Tissue
Adipose Tissue, White
Animals
Autonomic Pathways
Choline O-Acetyltransferase
Diabetes Mellitus
Humans
Immunohistochemistry
Male
Methods
Mice*
Models, Animal
Nerve Fibers
Peripheral Nerves*
Tyrosine 3-Monooxygenase
Choline O-Acetyltransferase
Tyrosine 3-Monooxygenase

Figure

  • Fig. 1 Quantitative comparison of peripheral nerves in adipose tissue from db/db diabetic mice versus those from db/− control mice. (A) Quantity of PGP 9.5 (protein gene product 9.5)-positive immunostained nerve fibers, expressed as the total nerve fiber area. (B) Ratios of the occupied areas of sympathetic and parasympathetic nerve fibers. (C) Tyrosine hydroxylase (TH; red) and choline acetyltransferase (ChAT; blue) immunohistochemistry staining results of sympathetic and parasympathetic nerve fibers, respectively. Data are presented as mean±standard deviation (n=10 per group). DM, diabetes mellitus. aP<0.05 vs. the normal group.


Reference

1. Kershaw EE, Flier JS. Adipose tissue as an endocrine organ. J Clin Endocrinol Metab. 2004; 89:2548–2556.
Article
2. Jang EH, Kim NY, Park YM, Kim MK, Baek KH, Song KH, Lee KW, Kwon HS. Influence of visceral adiposity on cardiovascular autonomic neuropathy in patients with type 2 diabetes mellitus. Diabetes Metab J. 2012; 36:285–292.
Article
3. Bittel DC, Bittel AJ, Tuttle LJ, Hastings MK, Commean PK, Mueller MJ, Cade WT, Sinacore DR. Adipose tissue content, muscle performance and physical function in obese adults with type 2 diabetes mellitus and peripheral neuropathy. J Diabetes Complications. 2015; 29:250–257.
Article
4. Voulgari C, Psallas M, Kokkinos A, Argiana V, Katsilambros N, Tentolouris N. The association between cardiac autonomic neuropathy with metabolic and other factors in subjects with type 1 and type 2 diabetes. J Diabetes Complications. 2011; 25:159–167.
Article
5. Fliers E, Romijn JA, Sauerwein HP, Kalsbeek A, Kreier F, Buijs RM. Adipose tissue: an innervated endocrine gland. Ned Tijdschr Geneeskd. 2002; 146:1976–1979.
6. Romijn JA, Fliers E. Sympathetic and parasympathetic innervation of adipose tissue: metabolic implications. Curr Opin Clin Nutr Metab Care. 2005; 8:440–444.
Article
7. Blaszkiewicz M, Townsend KL. Adipose tissue and energy expenditure: central and peripheral neural activation pathways. Curr Obes Rep. 2016; 5:241–250.
Article
8. Bartness TJ, Liu Y, Shrestha YB, Ryu V. Neural innervation of white adipose tissue and the control of lipolysis. Front Neuroendocrinol. 2014; 35:473–493.
Article
9. Kern PA, Ranganathan S, Li C, Wood L, Ranganathan G. Adipose tissue tumor necrosis factor and interleukin-6 expression in human obesity and insulin resistance. Am J Physiol Endocrinol Metab. 2001; 280:E745–E751.
Article
10. Marette A. Molecular mechanisms of inflammation in obesity-linked insulin resistance. Int J Obes Relat Metab Disord. 2003; 27:Suppl 3. S46–S48.
Article
11. Mokdad AH, Ford ES, Bowman BA, Dietz WH, Vinicor F, Bales VS, Marks JS. Prevalence of obesity, diabetes, and obesity-related health risk factors, 2001. JAMA. 2003; 289:76–79.
Article
12. Bamshad M, Aoki VT, Adkison MG, Warren WS, Bartness TJ. Central nervous system origins of the sympathetic nervous system outflow to white adipose tissue. Am J Physiol. 1998; 275(1 Pt 2):R291–R299.
13. Penicaud L, Cousin B, Leloup C, Lorsignol A, Casteilla L. The autonomic nervous system, adipose tissue plasticity, and energy balance. Nutrition. 2000; 16:903–908.
Article
14. Kreier F, Fliers E, Voshol PJ, Van Eden CG, Havekes LM, Kalsbeek A, Van Heijningen CL, Sluiter AA, Mettenleiter TC, Romijn JA, Sauerwein HP, Buijs RM. Selective parasympathetic innervation of subcutaneous and intra-abdominal fat--functional implications. J Clin Invest. 2002; 110:1243–1250.
Full Text Links
  • DMJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr