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Journal of anatomy1982; 135(Pt 1); 13-28;

The effects of thermal stimulation on the ultrastructure of the fundus and duct of the equine sweat gland.

Abstract: Sweating in the horse had little effect on the ultrastructure of the glandular duct, other than on the lumen which enlarged. The fundus secretory cells, which in the resting gland were packed with vesicles, gradually lost them as sweating progressed until, after 4 hours of activity, few remained. Sweat appeared to be largely the product of secretion (a) by fluid transport, probably involving a region of complex cellular interdigitations adjacent to the basement membrane and (b) by exocytosis of vesicles, although a secondary mechanism of vesicle loss by micro-apocrine secretion may occur. However, the products of cell death also contribute to sweat formation. The myoepithelium appeared contracted throughout. The function of the lower duct body, where complex basal infoldings of the luminal cells penetrated to the basement membrane, may differ from that of the upper portion. Dendritic Langerhans cells were found between the epithelia throughout the duct and fundus.
Publication Date: 1982-08-01 PubMed ID: 7130047PubMed Central: PMC1168125
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  • Journal Article

Summary

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This research evaluates how thermal stimulation, or heat, affects the structure and function of sweat glands in horses, highlighting the role of sweat glands in heat regulation, with particular emphasis on fluid transport and exocytosis in the secretion process.

Overview of the Research Study

  • The research was conducted on horses with particular focus on their sweat glands. The sweat glands of a horse are mainly divided into two parts: the fundus (the part that produces sweat) and the glandular duct (the tube that carries the sweat to the skin surface).
  • The study primarily investigated the ultrastructure (or detailed structure visible only with high-powered microscopes) of these regions of the sweat gland to understand their functional changes when the horse starts to sweat.

Effects of Sweating on the Sweat Gland

  • Upon thermal stimulation that causes the horse to sweat, the glandular duct’s lumen (the inside space of a tubular structure) enlarges.
  • Simultaneously, the secretory cells of the fundus undergo noticeable changes. At rest, these cells are densely packed with vesicles (small sac-like structures that store and transport substances). However, as the horse sweats, these vesicles gradually deplete. After about 4 hours of sweating, only a few remain.

Secretion Process and Fluid Transport

  • Sweat is considered to be predominately the product of two primary mechanisms: fluid transport and exocytosis of vesicles.
  • Fluid transport likely involves a complex network of cellular structures close to the basement membrane (a thin layer of cells at the bottom forming the base of the tissue).
  • In addition to these primary mechanisms, the study suggests the occurrence of a possible secondary mechanism, known as micro-apocrine secretion, which could contribute to the loss of vesicles.

Additional Observations

  • The study also suggests that products resulting from cell death may contribute to the formation of sweat.
  • Throughout the whole process, a structure called the myoepithelium (a type of muscle layer found in some glands) appears to remain contracted.
  • There is a change in function in the lower part of the duct, indicated by complex inward folds of the luminal cells penetrating the basement membrane.
  • The presence of dendritic Langerhans cells (a type of immune cell) was observed throughout the duct and fundus (gland’s body).

Implications

  • Findings from this study shed light on how horse sweat glands respond to heat and help to better understand the mechanism behind sweat production and secretion in horses.
  • These insights could be vital in developing strategies to manage horses in hot environments, potentially improving their comfort and performance.

Cite This Article

APA
Montgomery I, Jenkinson DM, Elder HY. (1982). The effects of thermal stimulation on the ultrastructure of the fundus and duct of the equine sweat gland. J Anat, 135(Pt 1), 13-28.

Publication

ISSN: 0021-8782
NlmUniqueID: 0137162
Country: England
Language: English
Volume: 135
Issue: Pt 1
Pages: 13-28

Researcher Affiliations

Montgomery, I
    Jenkinson, D M
      Elder, H Y

        MeSH Terms

        • Animals
        • Female
        • Horses / anatomy & histology
        • Hot Temperature
        • Male
        • Microscopy, Electron
        • Sweat Glands / metabolism
        • Sweat Glands / ultrastructure
        • Sweating
        • Vacuoles / ultrastructure

        References

        This article includes 19 references
        1. Munger BL. The cytology of apocrine sweat glands. I. Cat and monkey.. Z Zellforsch Mikrosk Anat 1965 Jul 30;67(3):373-89.
          pubmed: 4956654doi: 10.1007/BF00339383google scholar: lookup
        2. Hashimoto K, Gross BG, Lever WF. Electron microscopic study of apocrine secretion.. J Invest Dermatol 1966 Apr;46(4):378-90.
          pubmed: 5936042doi: 10.1038/jid.1966.58google scholar: lookup
        3. Robertshaw D, Taylor CR. Sweat gland function of the donkey (Equus asinus).. J Physiol 1969 Nov;205(1):79-89.
          pubmed: 5347721doi: 10.1113/jphysiol.1969.sp008952google scholar: lookup
        4. Allen TE, Bligh J. A comparative study of the temporal patterns of cutaneous water vapour loss from some domesticated mammals with epitrichial sweat glands.. Comp Biochem Physiol 1969 Oct 15;31(2):347-63.
          pubmed: 5353576doi: 10.1016/0010-406x(69)91659-4google scholar: lookup
        5. Sorensen VW, Prasad G. On the fine structure of horse sweat glands.. Z Anat Entwicklungsgesch 1973 Mar 20;139(2):173-83.
          pubmed: 4352229doi: 10.1007/BF00523636google scholar: lookup
        6. Jenkinson DM, Mabon RM. The effect of temperature and humidity on skin surface pH and the ionic composition of skin secretions in Ayrshire cattle.. Br Vet J 1973 May-Jun;129(3):282-95.
          pubmed: 4728197doi: 10.1016/s0007-1935(17)36482-5google scholar: lookup
        7. Bell M. Proceedings: The ultrastructure of human axillary apocrine glands after epinephrine injection.. J Invest Dermatol 1974 Jul;63(1):147-59.
          pubmed: 4834980doi: 10.1111/1523-1747.ep12678349google scholar: lookup
        8. Jenkinson DM, Montgomery I, Elder HY. Studies on the nature of the peripheral sudomotor control mechanism.. J Anat 1978 Mar;125(Pt 3):625-39.
          pubmed: 640964
        9. Jenkinson DM, Montgomery I, Elder HY. The ultrastructure of the sweat glands of the ox, sheep and goat during sweating and recovery.. J Anat 1979 Aug;129(Pt 1):117-40.
          pubmed: 511758
        10. SABATINI DD, BENSCH K, BARRNETT RJ. Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation.. J Cell Biol 1963 Apr;17(1):19-58.
          pubmed: 13975866doi: 10.1083/jcb.17.1.19google scholar: lookup
        11. REYNOLDS ES. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.. J Cell Biol 1963 Apr;17(1):208-12.
          pubmed: 13986422doi: 10.1083/jcb.17.1.208google scholar: lookup
        12. BIEMPICA L, MONTES LF. SECRETORY EPITHELIUM OF THE LARGE AXILLARY SWEAT GLANDS. A CYTOCHEMICAL AND ELECTRON MICROSCOPIC STUDY.. Am J Anat 1965 Jul;117:47-72.
          pubmed: 14345835doi: 10.1002/aja.1001170105google scholar: lookup
        13. KUROSUMI K, MATSUZAWA T, SAITO F. ELECTRON MICROSCOPIC OBSERVATIONS ON THE SWEAT GLANDS OF THE HORSE.. Arch Histol Jpn 1963 May;23:295-310.
          pubmed: 14046090doi: 10.1679/aohc1950.23.295google scholar: lookup
        14. Inoue T. Scanning electron microscopic study of the human axillary apocrine glands.. J Dermatol 1979 Oct;6(5):299-308.
        15. Sato K. Pharmacological responsiveness of the myoepithelium of the isolated human axillary apocrine sweat gland.. Br J Dermatol 1980 Sep;103(3):235-43.
        16. Montgomery I, Jenkinson DM, Elder HY. The ultrastructure of the sweat gland duct of the ox, sheep and goat before and during sweating.. J Anat 1982 Jun;134(Pt 4):741-55.
          pubmed: 7130038
        17. EVANS CL, NISBET AM, ROSS KA. A histological study of the sweat glands of normal and dry-coated horses.. J Comp Pathol 1957 Oct;67(4):397-405.
          pubmed: 13481174doi: 10.1016/s0368-1742(57)80039-3google scholar: lookup
        18. TAKAGI S, TAGAWA M. A cytological and cytochemical study of the sweat gland of the horse.. Jpn J Physiol 1959 Jun 25;9(2):153-9.
          pubmed: 13672687doi: 10.2170/jjphysiol.9.153google scholar: lookup
        19. MCLEAN JA. Measurement of cutaneous moisture vaporization from cattle by ventilated capsules.. J Physiol 1963 Jul;167(3):417-26.

        Citations

        This article has been cited 1 times.
        1. McDonald RE, Fleming RI, Beeley JG, Bovell DL, Lu JR, Zhao X, Cooper A, Kennedy MW. Latherin: a surfactant protein of horse sweat and saliva. PLoS One 2009 May 29;4(5):e5726.
          doi: 10.1371/journal.pone.0005726pubmed: 19478940google scholar: lookup