Abstract
It is known that parasympathetic nerve stimulation elevates venous pressure in the dog submandibular gland, and that the venous pressure wave is transformed to that of the arterial pulse. The vascular arrangements and histological characteristics of the dog submandibular gland were therefore examined to establish which anatomical structures are responsible for the change in venous pressure during salivation induced by parasympathetic stimulation. The acinar and ductal circulations were found to be arranged in parallel and arteriovenous anastomoses were identified in both. Microsphere injection studies demonstrated the opening of arteriovenous anastomoses in actively secreting glands. Smooth muscle cells were rarely found in venous blood vessels but venous valves were abundant in both circulations. Dense connective tissue was observed to enclose the ductal system and its accompanying structures (blood vessels, lymphatic vessels and nerves); it was most abundant in the hilum and diminished aborally. The mechanism responsible for elevating venous pressure during parasympathetic salivation is thus probably related to opening of the arteriovenous anastomoses; the increase in the amount of surrounding dense connective tissue in a central direction may facilitate the preservation of the transmitted arterial pressure and pulse in the venous system.
Full text
PDFImages in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BURGEN A. S., SEEMAN P. The role of the salivary duct system in the formation of the saliva. Can J Biochem Physiol. 1958 Jan;36(1):119–143. [PubMed] [Google Scholar]
- Blair-West J. R., Coghlan J. P., Denton D. A., Nelson J., Wright R. D., Yamauchi A. Ionic, histological and vascular factors in the reaction of the sheep's parotid to high and low mineralocorticoid status. J Physiol. 1969 Dec;205(3):563–579. doi: 10.1113/jphysiol.1969.sp008983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fraser P. A., Smaje L. H. The organization of the salivary gland microcirculation. J Physiol. 1977 Oct;272(1):121–136. doi: 10.1113/jphysiol.1977.sp012037. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fronek K., Zweifach B. W. Microvascular pressure distribution in skeletal muscle and the effect of vasodilation. Am J Physiol. 1975 Mar;228(3):791–796. doi: 10.1152/ajplegacy.1975.228.3.791. [DOI] [PubMed] [Google Scholar]
- Häggendal E., Sivertsson R. About arterio-venous shunts in salivary glands. A study with krypton elimination technique in dogs. Acta Physiol Scand. 1967 Sep;71(1):85–88. doi: 10.1111/j.1748-1716.1967.tb03712.x. [DOI] [PubMed] [Google Scholar]
- Lametschwandtner A., Lametschwandtner U., Weiger T. Scanning electron microscopy of vascular corrosion casts--technique and applications: updated review. Scanning Microsc. 1990 Dec;4(4):889–941. [PubMed] [Google Scholar]
- Lorber M. Branchings and course of the larger ducts and accompanying structures within the rat submandibular salivary gland. Am J Anat. 1991 Feb;190(2):133–156. doi: 10.1002/aja.1001900204. [DOI] [PubMed] [Google Scholar]
- Lung M. A. Variations in blood flow on mandibular glandular secretion to autonomic nervous stimulations in anaesthetized dogs. J Physiol. 1990 Dec;431:479–493. doi: 10.1113/jphysiol.1990.sp018341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lung M. A., Wang J. C. An anatomical investigation of the nasal venous vascular bed in the dog. J Anat. 1989 Oct;166:113–119. [PMC free article] [PubMed] [Google Scholar]
- Martin C. J., Young J. A. Electrolyte concentrations in primary and final saliva of the rat sublingual gland studied by micropuncture and catheterization techniques. Pflugers Arch. 1971;324(4):344–360. doi: 10.1007/BF00592462. [DOI] [PubMed] [Google Scholar]
- Maspers M., Björnberg J., Mellander S. Relation between capillary pressure and vascular tone over the range from maximum dilatation to maximum constriction in cat skeletal muscle. Acta Physiol Scand. 1990 Sep;140(1):73–83. doi: 10.1111/j.1748-1716.1990.tb08977.x. [DOI] [PubMed] [Google Scholar]
- Olesen S. P. An electrophysiological study of microvascular permeability and its modulation by chemical mediators. Acta Physiol Scand Suppl. 1989;579:1–28. [PubMed] [Google Scholar]
- SNELL R. S., GARRETT J. R. The effect of postganglionic sympathectomy on the structure of the submandibular and major sublingual salivary glands of the rat. Z Zellforsch Mikrosk Anat. 1958;48(6):639–652. doi: 10.1007/BF00398652. [DOI] [PubMed] [Google Scholar]
- Simionescu N., Simionescu M., Palade G. E. Open junctions in the endothelium of the postcapillary venules of the diaphragm. J Cell Biol. 1978 Oct;79(1):27–44. doi: 10.1083/jcb.79.1.27. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smaje L. H., Gamble J. Transcapillary transport during secretion by the rabbit submandibular salivary gland. J Dent Res. 1987 Feb;66(2):564–568. doi: 10.1177/00220345870660023001. [DOI] [PubMed] [Google Scholar]
- Smaje L., Zweifach B. W., Intaglietta M. Micropressures and capillary filtration coefficients in single vessels of the cremaster muscle of the rat. Microvasc Res. 1970 Jan;2(1):96–110. doi: 10.1016/0026-2862(70)90055-5. [DOI] [PubMed] [Google Scholar]
- Suddick R. P., Dowd F. J. The microvascular architecture of the rat submaxillary gland: possible relationship to secretory mechanisms. Arch Oral Biol. 1969 Jun;14(6):567–576. doi: 10.1016/0003-9969(69)90179-4. [DOI] [PubMed] [Google Scholar]
- Taira N., Satoh S. Differential effects of tetrodotoxin on the sialogenous and vasodilator actions of prostaglandin E2 in the dog salivary gland. Life Sci. 1974 Sep 1;15(5):987–993. doi: 10.1016/0024-3205(74)90013-7. [DOI] [PubMed] [Google Scholar]
- Tamarin A., Sreebny L. M. The rat submaxillary salivary gland. A correlative study by light and electron microscopy. J Morphol. 1965 Nov;117(3):295–352. doi: 10.1002/jmor.1051170303. [DOI] [PubMed] [Google Scholar]