Skip to main content
Log in

Effects of saturated fatty acids on amylase release from exocrine pancreatic segments of sheep, rats, hamsters, field voles and mice

  • Original Paper
  • Published:
Journal of Comparative Physiology B Aims and scope Submit manuscript

Abstract

Stimulatory effects of saturated fatty acids consisting of 4 (butyrate), 8 (octanoate), 12 (laurate) and 16 (palmitate) carbon atoms, as well as acetylcholine on pancreatic amylase release were assessed in tissue segments isolated from sheep, rats, hamsters, field voles and mice. The amount of amylase release induced by the fatty acids (1 μmol·l−1 to 10 mml·l−1) and by acetylcholine (10 nmol·l−1 to 100 μmol·l−1) increased in a concentration-dependent manner, and the maximum response in response to the fatty acids was obtained at the maximal dose used. The maximum increase in amylase release in response to butyrate or octanoate was highly and significantly (r=0.974,P<0.001) dependent on the log value of the mean body mass in the following order: sheep > rats > hamsters > field voles > mice. On the other hand, the response to laurate and palmitate was variable among animal species. Addition of atropine (1.4 μmol·l−1) to the medium did not reduce the responses to octanoate stimulation, but significantly reduced acetylcholine-induced responses implying that the effects of the fatty acids were not mediated through activation of muscarinic acetylcholine receptors. Reduction of calcium ion concentration in the medium significantly inhibited the responses induced by the fatty acids and acetylcholine, suggesting that amylase release depends on extracellular calcium ions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

Abbreviations

ACh :

acetylcholine

SCFA :

short-chain fatty acid(s)

HEPES :

N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid

HBSS :

HEPES-buffered saline solution

References

  • Amsterdam A, Jamieson JD (1972) Structural and functional characterization of isolated pancreatic cells. Proc Natl Acad Sci USA 69: 3082–3032

    Article  Google Scholar 

  • Bassett JM (1974) Diurnal patterns of plasma insulin, growth hormone, corticosteroid and metabolite concentrations in fed and fasted sheep. Aust J Biol Sci 27: 167–181

    PubMed  CAS  Google Scholar 

  • Harada E (1985) Comparison of pancreatic digestive enzyme secretion induced by volatile fatty acids in mice, Japanese field voles and goats. Comp Biochem Physicol 81A: 539–543

    CAS  Google Scholar 

  • Harada E, Kato S (1983) Effect of short-chain fatty acids on the secretory response of the ovine exocrine pancreas. Am J Physiol 244: G284-G290

    PubMed  CAS  Google Scholar 

  • Kato S, Katoh K, Barej W (1991) Regulation of exocrine pancreatic secretion in ruminants. In: Tsuda T et al. (eds) Physiological aspects of digestion and metabolism in ruminants. Academic Press. San Diego, USA, pp 89–109

    Google Scholar 

  • Katoh K (1994) The effect of short-chain fatty acids on the pancreas: endocrine and exocrine. In: Silverman E (ed). Short-chain fatty acids: metabolism and clinical importance. Report on the Tenth Ross Conference on Medical Research, Ross Laboratories, Columbus, USA, pp 74–77

  • Katoh K (1995) Effects of short-chain fatty acids on exocrine and endocrine pancreatic secretion. In: Cummings JH et al. (eds) Physiological and clinical aspects of short-chain fatty acids. Cambridge University Press, Cambridge, pp 223–231

    Google Scholar 

  • Katoh K, Ohbo M, Wakui M (1996) Octanoate increases cytosolic Ca2+ concentration and membrane conductance in ovine pancreatic acinar cells. J Comp Physiol B (in press)

  • Katoh K, Tsuda T (1984) Effects of short-chain fatty acids on acinar cells of the exocrine pancreas in sheep. J Physiol (Lond) 356: 479–489

    CAS  Google Scholar 

  • Katoh K, Tsuda T (1985) Effects of secretagogues on membrane potential and input resistance of pancreatic acinar cells of sheep. Res Vet Sci 38: 250–251

    PubMed  CAS  Google Scholar 

  • Katoh K, Tsuda T (1987) Effects of intravenous injection of butyrate on the exocrine pancreatic secretion in guinea pigs. Comp Biochem Physiol 87A: 569–572

    Article  CAS  Google Scholar 

  • Katoh K, Yajima T (1989) Effects of butyric acid and analogues on amylase release from pancreatic segments of sheep and goats. Pflügers Arch 413: 256–260

    Article  PubMed  CAS  Google Scholar 

  • Langer P, Snipes RL (1991) Adaptation of gut structure to function in herbivores. In: Tsuda T et al. (eds) Physiological aspects of digestion and metabolism in ruminants. Academic Press, San Diego, USA, pp 349–384

    Google Scholar 

  • Mineo H, Hashizume Y, Hanaki Y, Murata K, Maeda H, Onaga T, Kato S, Yanaihara N (1994) Chemical specificity of short-chain fatty acids in stimulating insulin and glucagon secretion in sheep. Am J Physiol 267: E234-E241

    PubMed  CAS  Google Scholar 

  • Ohbo M, Katoh K, Sasaki Y (1989) Effects of short-, medium- and long-chain fatty acids on amylase release from pancreatic segments of rats. Asian-Australasian J Anim Sci 2: 193–194

    Google Scholar 

  • Petersen OH (1992) Stimulus-secretion coupling: cytoplasmic calcium signals and the control of ion channels in exocrine acinar cells. J Physiol (Lond) 448: 1–51

    CAS  Google Scholar 

  • Sakata T (1995) Effects of short-chain fatty acids on the proliferation of gut epithelium cells in vitro. In: Cummings JH et al. (eds) Physiological and clinical aspects of short-chain fatty acids. Cambridge University Press, Cambridge, pp 289–305

    Google Scholar 

  • Stevens CE (1988) Microbial fermentation and synthesis of nutrients, and absorption of end products. In: Steven CE (ed) Comparative physiology of the vertebrate digestive system. Cambridge University Press, Cambridge, pp 159–190

    Google Scholar 

  • Wooten MW, Wrenn RW (1988) Linoleic acid is a potent activator of protein kinase C type III-α isoform in pancreatic acinar cells; its role in amylase release. Biochem Biophys Res Comm 153: 67–73

    Article  PubMed  CAS  Google Scholar 

  • Wrong OM (1995) Definition and history. In: Cummings JH et al. (eds) Physiological and clinical aspects of short-chain fatty acids. Cambridge University Press, Cambridge, pp 1–14

    Google Scholar 

  • Zar JH (1984) Biostatistical analysis, 2nd edn Prentice-Hall, Englewood Cliffs, pp 163–190

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to K. Katoh.

Additional information

Communicated by I.D. Hume

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ohbo, M., Katoh, K. & Sasaki, Y. Effects of saturated fatty acids on amylase release from exocrine pancreatic segments of sheep, rats, hamsters, field voles and mice. J Comp Physiol B 166, 305–309 (1996). https://doi.org/10.1007/BF02439916

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02439916

Key words