Preview

Journal of Anatomy and Histopathology

Advanced search

Age-Dependent Changes of Myenteric Nervous Plexus Histoarchitectonics in Proximal and Distal Colon of Wistar Rats

https://doi.org/10.18499/2225-7357-2017-6-3-75-81

Abstract

The aim of the study was to investigate the changes of the histoarchotectonics of the myenteric nervous plexus (MNP) in proximal and distal parts of colon in Wistar rats. Material and methods. The study was performed on 24 Wistar male rats (n=6 in each age group): newborns (3-4 days), prepubertal age (25-30 days), mature (3 months) and old (18-24 months). The colon was devided into proximal and distal sections. Histological, immunofluorescent and morphometric methods were used. Results. With the anti-βIII-tubulin immunofluorescence labeling we found an extensive growth of the myenteric plexus in the age period from the newborn to prepubertal animals, which was characterized with an increase in area of interganglionic spaces and an increase in thickness of interganglionic tracts. Age-related changes of the MNP, revealed with the anti-HuC/D and anti-S100b labeling, were characterized with a decrease in the relative number of ganglia and a proportional increase of their size, which was due to an increase in number of the axons or glial cells. There were no regional differences of histoarchitectonics of the MNP between the proximal and distal colon. Conclusions. In the period from newborn to prepubertal in male Wistar rats, intensive MNP growth is noted, characterized by an increase in the area of interganglionic spaces and thickness of the nerve tracts. Age changes in MNP are characterized by a decrease in the relative number of ganglia and a proportional increase in their size, which is obviously associated with an increase in the number of axons of neurons and glial cells. Histoarchitectonics of the MNP in the proximal and distal colon does not differ.

About the Authors

E. A. Tikhonov
Research institute of human morphology, Moscow, Russia
Russian Federation


O. V. Makarova
Research institute of human morphology, Moscow, Russia; Lomonosov Moscow State University, Moscow, Russia
Russian Federation


V. A. Golichenkov
Lomonosov Moscow State University, Moscow, Russia
Russian Federation


References

1. Ноздрачев А. Д. Физиология вегетативной нервной системы. Л.: Медицина; 1983.

2. Bitar K. N. V. Aging and gastrointestinal smooth muscle: from signal transduction to contractile proteins. American Journal of Physiology-Gastrointestinal and Liver Physiology. 2003; 284(1): G1-G7.

3. Blechman M. B., Gelb A. M. Aging and gastrointestinal physiology. Clinics in geriatric medicine. 1999; 15(3): 429-438.

4. Carloni M., et al. The impact of early life permethrin exposure on development of neurodegeneration in adulthood. Experimental gerontology. 2012; 47(1): 60-66.

5. Cossais F., et al. Postnatal development of the myenteric glial network and its modulation by butyrate. American Journal of Physiology-Gastrointestinal and Liver Physiology. 2016; 310(11): G941-G951.

6. Cowen T., et al. Restricted diet rescues rat enteric motor neurones from age related cell death. Gut. 2000; 47(5): 653-660.

7. Fehér E., Penzes L. Density of substance P, vasoactive intestinal polypeptide and somatostatin-containing nerve fibers in the ageing small intestine of the rats. Gerontology. 1987; 33(6): 341-348.

8. Furness J. B. The enteric nervous system and neurogastroenterology. Nature Reviews Gastroenterology and Hepatology. 2012; 9(5): 286-294.

9. Helander H. F. Morphological studies on the development of the rat colonic mucosa. Cells Tissues Organs. 1973; 85(2): 153-176.

10. Iacopetta B. Are there two sides to colorectal cancer? International journal of cancer. 2002; 101(5): 403-408.

11. Gabella G. Fall in the number of myenteric neurons in aging guinea pigs. Gastroenterology. 1989; 96(6): 1487-1493.

12. Geboes K., Collins S. Structural abnormalities of the nervous system in Crohn's disease and ulcerative colitis. Neurogastroenterology & Motility. 1998; 10(3): 189-202.

13. Liu M. T., et al. 5-HT4 receptor-mediated neuroprotection and neurogenesis in the enteric nervous system of adult mice. Journal of Neuroscience. 2009; 29(31): 9683-9699.

14. Matini P., Mayer B., Faussone-Pellegrini M. S. Neurochemical differentiation of rat enteric neurons during pre-and postnatal life. Cell and tissue research. 1997; 288 (1): 11-23.

15. Nagy N., Goldstein A. M. Enteric nervous system development: A crest cell’s journey from neural tube to colon. Seminars in Cell & Developmental Biology. Academic Press.; 2017.

16. Pácha J. Development of intestinal transport function in mammals. Physiological reviews. 2000; 80(4): 1633-1667.

17. Silva A. T., et al. Neural progenitors from isolated postnatal rat myenteric ganglia: expansion as neurospheres and differentiation in vitro. Brain research. 2008; 1218: 47-53.

18. Skinner S. A., O'Brien P. E. The microvascular structure of the normal colon in rats and humans. Journal of Surgical Research. 1996; 61(2): 482-490.

19. Young H. M., Bergner A. J., Müller T. Acquisition of neuronal and glial markers by neural crest-derived cells in the mouse intestine. Journal of Comparative Neurology. 2003; 456(1): 1-11.


Review

For citations:


Tikhonov E.A., Makarova O.V., Golichenkov V.A. Age-Dependent Changes of Myenteric Nervous Plexus Histoarchitectonics in Proximal and Distal Colon of Wistar Rats. Journal of Anatomy and Histopathology. 2017;6(3):75-81. (In Russ.) https://doi.org/10.18499/2225-7357-2017-6-3-75-81

Views: 387


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2225-7357 (Print)