Impact of Autonomic Tonus Typological Features on the Duodenum Structure of Chickens
DOI:
https://doi.org/10.17140/VMOJ-1-103Keywords:
Autonomous tone; Chicken; Intestinal wall; MorphometryAbstract
The goal of this research is to show the relationship between the duodenum morphology of
laying hens (Gallus domesticus) of ISA Brown cross and typological peculiarities of autonomic
tonus in the poultry organism. To achieve the goal a group of adult chickens (aged one year)
was investigated to determine an aggregate tonus of their autonomic centers based on the study
of heart rate variability (variation pulsometry). According to the results all the poultry was
divided into two groups: sympatheticotonic chickens (hereinafter referred to as ST chickens)
and sympathetico-normotonic chickens (hereinafter referred to as ST-NT chickens) The first
group of poultry is characterized by a clear predominance of sympathetic centers tonus while
within the second group there is a slightly increased tonus of parasympathetic centers. Using
a set of various morphological methods a comparative analysis of the duodenum structure in
these groups was made. The analysis revealed that ST chickens unlike ST-NT chickens are
characterized by a higher value of the duodenum absolute length (by 1.6 cm) and its relative
length (by 1.4 %) as well as lower values of its internal perimeter (by 0, 25 cm). Apart from
this, an increase of absorption surface of the duodenum mucous membrane is observed in STNT chickens. Increase in villus height (by 143.7 micrometers) and their quantity (by 61.5) per
1sm2 contribute greatly to it. In the duodenum muscle membrane the thickness of both layers
has larger values under a distinct sympathetic tonus in ST-NT chickens. In a circular layer
difference between poultry groups reaches 21 micrometers while in a longitudinal it approaches
4.9 micrometers. Investigating a connective tissue it was found that the relative area of its fibers
near the mucosal crypts of ST chickens is larger by 0.21 % than that of the ST-NT chicken. In
the muscle layer area a superiority of ST chickens according to this indicator reduces to 0.15%.
References
Hughes RJ. Energy metabolism in chickens: Physiological limitations. Adelaide, SA, Australia: Rural Industries Research and Development Corporation; 2003: 1-62.
Karaca T, Yörük M. A morphological and histometrical study on distribution and heterogeneity of mast cells of chicken’s and quail’s digestive tract. YYU Vet Fak Derg. 2004; 15(1-2): 115-121. Web site. http://vfdergi.yyu.edu.tr/archive/2004/15_1-2/2004_15_(1-2)_ 115-121.pdf. Accessed March 28, 2016
Duke GE. Gastrointestinal physiology and nutrition in wild birds. Proc Nutr Soc. 1997; 56(3): 1049-1056. doi: 10.1079/ PNS19970109
Nasrin M, Siddiqi MNH, Masum MA, Wares MA. Gross and histological studies of digestive tract of broilers during postnatal growth and development. J Bangladesh Agril Univ. 2012; 10(1): 69-77. doi: 10.3329/jbau.v10i1.12096
Shih BL, Chen Y-H, Hsu J-C. Morphological development of the small intestine in white Roman goslings. Afr J Biotechnol. 2013; 12(6): 611-617. doi: 10.5897/AJB11.1526
Kadhim KK, Bakar MZA, Noordin MM, Babjee MA, Saad MZ. Light and scanning electron microscopy of the small intestine of young malaysian village chicken and commercial broiler. Pertanika J Trop Agric Sci. 2014; 37(1): 51-64.
Mott CR, Siegel PB, Webb KE Jr, Wong EA. Gene expression of nutrient transporters in the small intestine of chickens from lines divergently selected for high or low juvenile body weight. Poultry Sci. 2008; 87(11): 2215-2224. doi: 10.3382/ps.2008-00101
Mahmud MA, Shaba P, Shehu SA, Danmaigoro A, Gana J, Abdussalam W. Gross morphological and morphometric studies on digestive tracts of three nigerian indigenous genotypes of chicken with special reference to sexual dimorphism. J. World’s Poult Res. 2015; 5(2): 32-41. Web site. http://agris.fao.org/agris-search/ search.do?recordID=IR2015400050. Accessed March 28, 2016
Oliveira JE, Druyan S, Uni Z, Ashwell CM, Ferket P.R. Prehatch intestinal maturation of turkey embryos demonstrated through gene expression patterns. Poultry Sci. 2009; 88(12): 2600-2609. doi: 10.3382/ps.2008-00548
Fisinin VI, Suraj P. Gut immunity in birds: facts and reflections (review). Agricultural Вiology. 2013; 4: 3-25. Web site. http:// cyberleninka.ru/article/n/gut-immunity-in-birds-facts-and-reflections-review. Accessed March 28, 2016
Horra MCDL, Cano M, Peral MJ, Calonge ML, Ilundain AA. Hormonal regulation of chicken intestinal NHE and SGLT-1 activities. Am J Physiol Regulatory Integrative Comp Physiol. 2001; 280: 655-660. Web site. http://ajpregu.physiology.org/ content/280/3/R655.short. Accessed March 28, 2016
Muir WI, Bryden WL, Husband AJ. Immunity, vaccination and the avian intestinal tract. Dev Comp Immunol. 2000; 24(2-3): 325- 342. doi: 10.1016/S0145-305X(99)00081-6
Rawdon B.B. Gastrointestinal hormones in birds: Morphological, chemical, and developmental aspects. J Exp Zool. 1984; 232(3): 659-670. doi: 10.1002/jez.1402320335
Vylitova M, Miksik I, Pacha J. Metabolism of corticosterone in mammalian and avian intestine. Gen Comp Endocrinol. 1998; 109(3): 315-324. doi: 10.1006/gcen.1997.7035
Stappenbeck TS, Hooper LV, Gordon JI. Developmental regulation of intestinal angiogenesis by indigenous microbes via Paneth cells. PNAS. 2002; 99(24): 15451-15455. doi: 10.1073/ pnas.202604299
Dibner JJ, Richards JD. The digestive system: Challenges and opportunities. J Appl Poult Res. 2004; 13(1): 86-93. doi: 10.1093/ japr/13.1.86
Adil S, Banday T, Ahmad Bhat G, Salahuddin M, Raquib M, Shanaz S. Response of broiler chicken to dietary supplementation of organic acids. JCEA. 2011; 12(3): 498-508 doi: 10.5513/ JCEA01/12.3.947
Incharoen T. Histological adaptations of the gastrointestinal tract of broilers fed diets containing insoluble fiber from rice hull meal. Am J Anim Vet Sci. 2013; 8(2): 79-88. doi: 10.3844/ ajavssp.2013.79.88
Revajová V, Slaminková Z, Grešáková Ľ, Levkut M.Duodenal morphology and immune responses of broiler chickens fed low doses of deoxynivalenol. Acta Vet Brno. 2013; 82: 337-342. doi: 10.2754/avb201382030337
Pelicano ERL, Souza PA, Souza HBA, Figueiredo DF, Amaral CMC. Morphometry and ultra-structure of the intestinal mucosa of broilers fed different additives. Rev Bras Cienc Avic. 2007; 9(3): 173-180. doi: 10.1590/S1516-635X2007000300006
Sittiya J, Yamauchi K. Growth performance and histological intestinal alterations of sanuki cochin chickens fed diets diluted with untreated whole-grain paddy rice. J Poult Sci. 2014; 51(1): 52-57. doi: 10.2141/jpsa.0130042
Bar-Shira E, Cohen I, Elad O, Friedman A. Role of goblet cells and mucin layer in protecting maternal IgA in precocious birds. Dev Comp Immunol. 2014; 44(1): 186-194. doi: 10.1016/j. dci.2013.12.010
Shao Y, Guo Y, Wang Z. β-1,3/1,6-Glucan alleviated intestinal mucosal barrier impairment of broiler chickens challenged with Salmonella enterica serovar Typhimurium. Poult Sci. 2013; 92(7): 1764-1773. doi: 10.3382/ps.2013-03029
Zhang, B., Shao Y, Liu D, Yin P, Guo Y, Yuan J. Zinc prevents Salmonella enterica serovar Typhimurium-induced loss of intestinal mucosal barrier function in broiler chickens. Avian Pathol. 2012; 41(4): 361-367. doi: 10.1080/03079457.2012.692155
Baevskij RM. Analiz variabel’nosti serdechnogo ritma: istorija i filosofija, teorija i praktika [Analysis of heart rate variability: the history and philosophy, theory and practice]. Klinicheskaja informatika i telemedicina [Clinical informatics and telemedicine]. 2004; 1: 54-64. (Rus.)
Baevskij RM, Kirilov OI, Kleckin SZ. Matematicheskij analiz izminenij serdechnogo ritma pri stresse [Mathematical analysis of changes in heart rate during stress]. Moscow. USSR: Nauka, 1984. (Rus.)
Hart rate variability. Standarts of measurements, physiological interpretation, and clinical use. Task force of the european of cardiology and the north american society of pacing and electrophysiology. Circulation. 1996; 93: 1043-1065. doi: 10.1161/01.CIR.93.5.1043
Mulisch M, Welsch U. Romeis - Mikroskopische Technik. Spektrum akademischer verlag; 2010. doi: 10.1007/978-3-8274- 2254-5
Yovchev D, Dimitrov D, Penchev G. Age weight and morphometrical parameters of the bronze turkey’s (Meleagris meleagris gallopavo) intestines. Bulg J Agric Sci. 2013; 19(3): 611- 614. Web site. http://www.agrojournal.org/19/03-36.pdf. Accessed March 28, 2016
Kadhim KK, Zuki ABZ, Noordin MM, Babjee SA, Khamas W. Growth evaluation of selected digestive organs from day one to four months post-hatch in two breeds of chicken known to differ greatly in growth rate. Journal of Animal and Veterinary Advances. 2010; 9(6): 995-1004. doi: 10.3923/javaa.2010.995.1004
Yamauchi K. Review on chicken intestinal villus histological alterations related with intestinal function. J Poult Sci. 2002; 39(4): 229-242. doi: 10.2141/jpsa.39.229
Mitjans M, Barniol G, Ferrer R. Mucosal surface area in chicken small intestine during development. Cell Tissue Res. 1997; 290(1): 71-78. doi: 10.1007/s004410050909
Pelicano ERL, Souza PA, Souza HBA, et al. Intestinal mucosa development in broiler chickens fed natural growth promoters. Brazilian Journal of Poultry Science. 2005; 7(4): 221-229. doi: 10.1590/S1516-635X2005000400005
Awad W, Ghareeb K, Böhm J. Intestinal structure and function of broiler chickens on diets supplemented with a synbiotic containing enterococcus faecium and oligosaccharides. Int J Mol Sci. 2008; 9(11): 2205-2216. doi: 10.3390/ijms9112205
Laudadio V, Passantino L, Perillo A, et al. Productive performance and histological features of intestinal mucosa of broiler chickens fed different dietary protein levels. Poultry Sci. 2012; 91(1): 265-270. doi: 10.3382/ps.2011-01675
Wali ON, Kadhim KK. Histomorphological comparison of proventriculus and small intestine of heavy and light line pre- and at hatching. Int J Anim Veter Adv. 2014; 6(1): 40-47. Web site. http://www.airitilibrary.com/Publication/alDetailedMesh?docid =20412908-201402-201507200026-201507200026-40-47. Accessed March 28, 2016
Clench MH, Mathias JR. Motility responses to fasting in the gastrointestinal tract of three avian species. The condor. 1995; 97(4): 1041-1047. doi: 10.2307/1369542
Hodgkiss JP. Intrinsic reflexes underlying peristalsis in the small intestine of the domestic fowl. J Physiol. 1986; 380(1): 311- 328. doi: 10.1113/jphysiol.1986.sp016287
Downloads
Published
How to Cite
Issue
Section
License

This work is licensed under a Creative Commons Attribution 4.0 International License.
All content published in Veterinary Medicine (VM) is licensed under the Creative Commons Attribution 4.0 International License (CC BY 4.0). This license allows anyone to copy, distribute, transmit, and adapt the work — including for commercial purposes — provided appropriate credit is given to the original author(s) and source.