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Activity of Digestive Enzymes in the American Mink (Neovison vison) Selected for Tameness and Defensive Aggression toward Humans

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Abstract

Selection of animals for a defensive reaction toward humans underlies the domestication of species and leads to genome destabilization, as well as restructuring of the nervous and hormonal systems that regulate many physiological functions, including digestion . The aim was to study the activity of digestive enzymes (amylase, lipase and proteases) in the pancreas, duodenum and jejunum of the American mink (Neovison vison) of two behavioral types, aggressive and tame. Our findings suggest that pleiotropic effects of behavioral genes are also involved in the regulation of digestive enzyme activity in the American mink. Despite the same diet, aggressive vs. tame animals were characterized by a higher activity of proteases and lipase, whereas in tame minks, the amylolytic profile of digestive enzyme activity was predominant. Discriminant analysis confirmed the differences between aggressive and tame minks, but not between the two groups of aggressive animals, in terms of the parameters studied. The revealed differences in the profile of the activity of digestive enzymes can be associated with mutations in the enzyme genes, as well as mediated action of hormones involved in stress reactivity.

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REFERENCES

  1. Trapezov OV (2000) Behavioural polymorphism in defensive behaviour towards man in farm raised mink (Mustela vison Schreber, 1777). Scientifur 24: 103–109.

    Google Scholar 

  2. Wilkins AS, Wrangham RW, Fitch WT (2014) The “domestication syndrome” in mammals: a unified explanation based on neural crest cell behavior and genetics. Genetics 197(3): 795–808. https://doi.org/10.1534/genetics.114.165423

    Article  PubMed  PubMed Central  Google Scholar 

  3. Belyaev DK (1979) Destabilizing selection as a factor in domestication. J Heredity 70: 301–308.

    Article  CAS  Google Scholar 

  4. Giammanco M, Tabacchi G, Giammanco S, Di Majo D, La Guardia M (2005) Testosterone and aggressiveness. Medical Science Monitor 11(4): RA136–RA145.

    CAS  PubMed  Google Scholar 

  5. Veenema AH, Cremers TI, Jongsma ME, Steenbergen PJ, de Boer SF, Koolhaas JM (2005) Differences in the effects of 5-HT 1A receptor agonists on forced swimming behavior and brain 5-HT metabolism between low and high aggressive mice. Psychopharmacology 178(2): 151–160. https://doi.org/10.1007/s00213-004-2005-5

    Article  CAS  PubMed  Google Scholar 

  6. Albert FW, Shchepina O, Winter C, Römpler H, Teupser D, Palme R, Ceglarek U, Kratzsch J, Sohr R, Trut LN, Thiery J, Morgenstern R, Plyusnina L, Schöneberg T, Pääbo S (2008) Phenotypic differences in behavior, physiology and neurochemistry between rats selected for tameness and for defensive aggression towards humans. Hormones and behavior 53(3): 413–421. https://doi.org/10.1016/j.yhbeh.2007.11.010

    Article  CAS  PubMed  Google Scholar 

  7. Eusebi PG, Sevane N, O’Rourke T, Pizarro M, Boeckx C, Dunner S (2021) Gene expression profiles underlying aggressive behavior in the prefrontal cortex of cattle. BMC genomics 22(1): 1–14. https://doi.org/10.1186/s12864-021-07505-5

    Article  CAS  Google Scholar 

  8. Kitchener AC (1998) The Scottish wildcat—a cat with an identity crisis? British Wildlife 9: 232–242.

    Google Scholar 

  9. Axelsson E, Ratnakumar A, Arendt M, Maqbool K, Webster MT, Perloski M, Liberg O, Arnemo JM, Hedhammarå LK (2013) The genomic signature of dog domestication reveals adaptation to a starch-rich diet. Nature 495: 360–364. https://doi.org/10.1038/nature11837

    Article  CAS  PubMed  Google Scholar 

  10. Gugolek A, Strychalski J, Konstantynowicz M, Zwolinski C (2014) Comparative analysis of nutrient digestibility and nitrogen retention in wild and farmed canids. Annals of Animal Science 14(2): 307–314. https://doi.org/10.2478/aoas-2014-0002

    Article  CAS  Google Scholar 

  11. Kulikov AV, Bazhenova EY, Kulikova EA, Fursenko DV, Trapezova LI, Terenina EE, Mormede P, Popova NK, Trapezov OV (2016) Interplay between aggression, brain monoamines and fur color mutation in the American mink. Genes, Brain and Behavior 15(8): 733–740. https://doi.org/10.1111/gbb.12313

    Article  CAS  Google Scholar 

  12. Trapezov OV (2000) Behavioural polymorphism in defensive behaviour towards man in farm raised mink (Mustela vison Schreber, 1777). Scientifur 24(2): 103–109.

    Google Scholar 

  13. Fitzhugh DC, Parmer A, Shelton LJ, Sheets JT (2008) A comparative analysis of carbon dioxide displacement rates for euthanasia of the ferret. Lab Anim (NY) 37: 81–86. https://doi.org/10.1038/laban0208-81

  14. Oleinik VM (1995) Distribution of digestive enzyme activities along intestine in blue fox, mink, ferret and rat. Comp Biochem Physiol A 112(1): 55–58.

    Article  CAS  Google Scholar 

  15. Sangild PT, Elnif J (1996) Intestinal hydrolytic activity in young mink (Mustela vison) develops slowly postnatally and exhibits late sensitivity to glucocorticoids. J Nutr 126(9): 2061–2068. https://doi.org/10.1093/jn/126.9.2061

    Article  CAS  PubMed  Google Scholar 

  16. Kohl KD, Ciminari ME, Chediack JG, Leafloor JO, Karasov WH, McWilliams SR, Caviedes-Vidal E (2017) Modulation of digestive enzyme activities in the avian digestive tract in relation to diet composition and quality. J Comp Physiol B 187: 339–351. https://doi.org/10.1007/s00360-016-1037-6

    Article  CAS  PubMed  Google Scholar 

  17. Eisert R (2011) Hypercarnivory and the brain: protein requirements of cats reconsidered. J Comp Physiol B 181(1): 1–17. https://doi.org/10.1007/s00360-010-0528-0

    Article  CAS  PubMed  Google Scholar 

  18. Skrede A, Berge GM, Storebakken T, Herstad O, Aarstad KG, Sundstøl F (1998) Digestibility of bacterial protein grown on natural gas in mink, pigs, chicken and Atlantic salmon. Anim Feed Sci Technol 76(1–2): 103–116. https://doi.org/10.1016/S0377-8401(98)00208-9

    Article  CAS  Google Scholar 

  19. Buddington RK, Malo C, Sangild PT, Elnif J (2000) Intestinal transport of monosaccharides and amino acids during postnatal development of mink. Am J Physiol Regulatory Integrative Comp Physiol 279: R2287–R2296. https://doi.org/10.1152/ajpregu.2000.279.6.R2287

    Article  CAS  Google Scholar 

  20. Flynn NE, Wu G (1997) Enhanced metabolism of arginine and glutamine in enterocytes of cortisol-treated pigs. Am J Physiol Gastrointest Liver Physiol 272: G474–G480. https://doi.org/10.1152/ajpgi.1997.272.3.G474

    Article  CAS  Google Scholar 

  21. Elnif J, Buddington RK, Hansen NE, Sangild PT (2006) Cortisol increases the activities of intestinal apical membrane hydrolases and nutrient transporters before weaning in mink (Mustela vison). J Comp Physiol B 176(3): 233–241. https://doi.org/10.1007/s00360-005-0044-9

    Article  CAS  PubMed  Google Scholar 

  22. Pajic P, Pavlidis P, Dean K, Neznanova L, Romano RA, Garneau D, Daugherity E, Globig A, Ruhl S, Gokcumen O (2019) Independent amylase gene copy number bursts correlate with dietary preferences in mammals. Elife 8: e44628. https://doi.org/10.7554/eLife.44628

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Svechkina EB, Tjutjunnik NN (2007) Changes in digestive enzymes’ activity of various genotypes of American mink (Mustela vison Schreber, 1777) during the process of domestication. Informacionnyj Vestnik VOGiS 11(1): 99–108 (In Russ).

    Google Scholar 

  24. Corring T (1980) The adaptation of digestive enzymes to the diet: its physiological significance. Reprod Nurr Devel 20: 1217–1235. https://doi.org/10.1051/rnd:19800713

    Article  CAS  Google Scholar 

  25. Harada E, Kato S (1982) Influence of adrenaline, glucagon, hydrocortisone, thyroxine, or insulin administration on pancreatic exocrine secretion in rats. Jpn J Vet Sci 44: 589–596.

    Article  CAS  Google Scholar 

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ACKNOWLEDGMENTS

The authors express their gratitude to the associates of the Laboratory of ecological physiology of animals (IB FRC KRC), especially to Dr. E.A. Khizhkin, for his assistance in conducting the experiment.

Funding

This work was supported by the Federal budget within the assignment to the IB FRC KarRC RAS (FMEN-2022-0003) and the ICG SB RAS project No. 0259-2021-0015.

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Authors

Contributions

Basic idea and experimental design (O.V.T., V.A.I., S.N.K.), animal handling and biomaterial collection (O.V.T., L.I.T., S.N.K., M.A.N., M.A.S., E.A.S.), laboratory analyses (A.V.M.), data processing (V.A.I., S.N.K.), writing and editing the manuscript (S.N.K., V.A.I., O.V.T.).

Corresponding author

Correspondence to S. N. Kalinina.

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CONFLICT OF INTEREST

The authors declare that they have no conflict of interest associated with the publication of this article.

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Translated by A. Polyanovsky

Russian Text © The Author(s), 2022, published in Zhurnal Evolyutsionnoi Biokhimii i Fiziologii, 2022, Vol. 58, No. 1, pp. 61–68https://doi.org/10.31857/S0044452922010028.

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Kalinina, S.N., Ilyukha, V.A., Trapezov, O.V. et al. Activity of Digestive Enzymes in the American Mink (Neovison vison) Selected for Tameness and Defensive Aggression toward Humans. J Evol Biochem Phys 58, 64–72 (2022). https://doi.org/10.1134/S0022093022010069

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