Skip to main content
Log in

A light and electron microscopic examination of the vagal hepatic branch of the rat

  • Published:
Anatomy and Embryology Aims and scope Submit manuscript

Summary

The rat's vagal hepatic branch and associated tissues were studied using light and electron microscopy. Whole mounts, serial sections, and vascular endocasts were used to characterize the tissue from the anterior vagal trunk to the porta hepatis. Fiber number and caliber as well as intraneural organization were analyzed from complete cross-sectional electron micrographic montages of the hepatic branch sampled at its point of separation from the anterior vagal trunk.

The hepatic branch ramified from the anterior vagus in one (in 47% of the specimens), two (in 37%) or three (in 16%) bundles. The single bundled hepatic branch contained 2887±287 unmyelinated fibers, and their size distribution, with a mean diameter of 0.66±0.02 μm, was Gaussian. Myelinated fibers numbered only 21±4 per branch and had a complex size distribution ranging from 0.5 to 1.8 μm with a mean of 1.2±0.03 μm. Forty four ±6% of the myelinated fibers were found in a single “subfascicle” in the dorso-medial pole of the nerve. Whole mounts at this level revealed that a distinct bundle, here designated an extrinsic “hepato-gastric bundle”, occurred within the hepatic branch and linked the omental hepatic branch and the distal anterior gastric branch, apparently without central vagal connections. In the lesser omentum, between the esophagus and the hepatic artery proper, the hepatic branch formed a plexus which was characterized by numerous nerve divisions, anastomoses and large paraganglia (196–463 glomus cells per paraganglion). This plexiform segment ended with the recombining of the hepatic branch into 5–7 bundles which variously ascended in the porta, descended on the hepatic artery proper, or traversed the portal vein. Through its omental course, the hepatic branch traveled in close apposition to the hepato-esophageal artery and the corresponding vein as well as a prominent lymphatic vessel with associated hemolymph nodes.

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

Access this article

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

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Agostoni E, Chinnock JE, De Burgh Daly M, Murray JG (1957) Functional and histological studies of the vagus nerve and its branches to the heart, lungs and abdominal viscera in the cat. J Physiol 135:182–205

    Google Scholar 

  • Ahlman BHJ, Larson GM, Bombeck CT, Nyhus LM (1979) Origin of the adrenergic fibers in the subdiaphragmatic vagus of the dog. Am J Surg 137:116–122

    Google Scholar 

  • Barja F, Mathison R (1984) Sensory innervation of the rat portal vein and the hepatic artery. J Auton Nerv Syst 10:117–125

    Google Scholar 

  • Boekelaar AB (1985) The extrinsic innervation of the stomach and other upper abdominal organs in the rat. Doctoral Thesis, Faculteit der Wiskunde en Natuurwetenschapen, Universiteit van Amsterdam, pp 1–94

  • Dahlqvist A, Carlsoo B, Hellstrom S (1982) Fiber components of the recurrent laryngeal nerve of the rat: a study by light and electron microscopy. Anat Rec 204:365–370

    Google Scholar 

  • Deane BM, Howe A, Morgan M (1975) Abdominal vagal paraganglia: distribution and comparison with carotid body in the rat. Acta Anat 93:19–28

    Google Scholar 

  • Evans DHL, Murray JG (1959) Histological and functional studies on the fibre composition of the vagus nerve of the rabbit. J Anat 93:9–14

    Google Scholar 

  • Firbas VW, Sinzinger H, Hohenecker J (1972) Die unpaaren Aste der Aorta abdominalis und die arterielle Versorgung der Leber bei der Laboratoriumsratte und der Laboratoriumsmaus. Säugetierkdl Mitteil 20:359–366

    Google Scholar 

  • Fox EA, Powley TL (1985) Longitudinal columnar organization within the dorsal motor nucleus represents separate branches of the abdominal vagus. Brain Res 341:269–282

    Google Scholar 

  • Gabella G, Pease HL (1973) Number of axons in the abdominal vagus of the rat. Brain Res 58:465–469

    Google Scholar 

  • Goormaghtigh N (1936) On the existence of abdominal vagal paraganglia in the adult mouse. J Anat 71:77–90

    Google Scholar 

  • Graffner H, Elelund M, Hakanson R, Rosengren E (1985) Effect of different denervation procedures on catecholamines in the gut. Scand J Gastroenterol 20:1276–1280

    Google Scholar 

  • Griffith CA (1969) Significant functions of the hepatic and celiac vagi. Am J Surg 118:251–259

    Google Scholar 

  • Kemp DR (1973) A histological and functional study of the gastric mucosal innervation in the dog Part I: The quantification of the fiber content of the normal subdiaphragmatic vagal trunks and their abdominal branches. Aust N Z J Surg 43:288–293

    Google Scholar 

  • Kuntz A, Jacobs MW (1955) Components of periarterial extensions of celiac and mesenteric plexuses. Anat Rec 123:509–520

    Google Scholar 

  • Lautt WW (1983) Afferent and efferent neural roles in liver function. Prog Neurobiol 21:323–348

    Google Scholar 

  • Lee KC (1985) Reflex suppression and initiation of gastric contractions by electrical stimulation of the hepatic vagus nerve. Neurosci Lett 53:57–62

    Google Scholar 

  • Leneman F, Burton S (1967) The hepato-esophageal artery of the rat. Acta Anat 68:334–343

    Google Scholar 

  • Loeweneck H (1974) Functional anatomy of the vagus nerves in the upper abdomen. In: Holle F, Andersson S (eds) Vagotomy, Springer, New York Heidelberg Berlin

    Google Scholar 

  • Magni F, Carobi C (1983) The afferent and preganglionic parasympathetic innervation of the rat liver, demonstrated by retrograde transport of horseradish peroxidase. J Auton Nerv System 8:237–260

    Google Scholar 

  • McCrea ED (1924) The abdominal distribution of the vagus. J Anat 59:15–40

    Google Scholar 

  • McDonald DM (1983) Morphology of the rat carotid sinus nerve. II. Number and size of axons. J Neurocytol 12:373–392

    Google Scholar 

  • McDonald DM, Blewett RM (1981) Location and size of carotid body-like organs (paraganglia) revealed in rats by the permeability of blood vessels to Evans blue dye. J Neurocytol 10:607–643

    Google Scholar 

  • McDonald DM, Mitchell RA (1975) The innervation of glomus cells, ganglion cells and blood vessels in the rat carotid body: a quantitative ultrastructural analysis. J Neurocytol 4:177–230

    Google Scholar 

  • Morgan M, Pack RJ, Howe A (1976) Structure of cells and nerve endings in abdominal vagal paraganglia of the rat. Cell Tissue Res 169:467–484

    Google Scholar 

  • Nagata H, Guth PH (1984) In vivo observation of the lymphatic system in the rat stomach. Gastroenterology 86:1443–1450

    Google Scholar 

  • Niijima A (1983) Electrophysiological study on nervous pathway from splanchnic nerve to vagus nerve in rat. Am J Physiol 13:R888-R890

    Google Scholar 

  • Nopajaroonsri C, Luk SC, Simon GT (1974) The structure of the hemolymph node — a light, transmission, and scanning electron microscopic study. J Ultrastruc Res 48:325–341

    Google Scholar 

  • Olin T, Saldeen T (1964) The lymphatic pathways from the peritoneal cavity: a lymphangiographic study in the rat. Cancer Res 24:1700–1711

    Google Scholar 

  • Precht JC, Powley TL (1985) Organization and distribution of the rat subdiaphragmatic vagus and associated paraganglia. J Comp Neurol 235:182–195

    Google Scholar 

  • Prechtl JC, Powley TL (1986) A versatile method for analyzing autonomic nerve connectivity. 16th Annual Meeting Society For Neuroscience 12:# 321.10

  • Reynolds ES (1963) The use of lead citrate at high pH as an electron opaque stain in electron microscopy. J Cell Biol 17:208–212

    Google Scholar 

  • Richter CP, Rice KK (1942) The effect of thiamine hydrochloride on the energy value of dextrose studied in rats by the single food choice method. Am J Physiol 137:573–581

    Google Scholar 

  • Roberts WJ, Elardo SM (1986) Clustering of primary afferent fibers in peripheral nerve fascicles by sensory modality. Brain Res 370:149–152

    Google Scholar 

  • Rogers RC, Kahrilas PJ, Hermann GE (1984) Projection of the hepatic branch of the splanchnic nerve to the brainstem of the rat. J Auton Nerv Syst 11:223–225

    Google Scholar 

  • Ruckley CV (1964) A study of the variations of the abdominal vagi. Brit J Surg 51:569–573

    Google Scholar 

  • Sakaguchi T, Yamaguchi K (1978) Changes in efferent activities of the gastric vagus nerve by administration of glucose in the portal vein. Experientia 35:875–876

    Google Scholar 

  • Sawchenko PE, Friedman MI (1979) Sensory functions of the liver —A review. Am J Physiol 236:R5-R20

    Google Scholar 

  • Sunderland S (1980) The anatomical basis of nerve repair. In: Jewett DL, McCarroll HR (eds) Nerve repair and regeneration: Its clinical and experimental basis. C.V. Mosby Co., St. Louis Toronto London

    Google Scholar 

  • Swett JE, Bourassa CM (1981) Electrical stimulation of peripheral nerve. In: Patterson MM, Kesner RP (eds) Electrical stimulation research techniques, Academic Press, NY

    Google Scholar 

  • Williams RW, Chalupa LM (1983) An analysis of axon caliber within the optic nerve of the cat: Evidence of size groupings and regional organization. J Neurosci 3:1554–1564

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Prechtl, J.C., Powley, T.L. A light and electron microscopic examination of the vagal hepatic branch of the rat. Anat Embryol 176, 115–126 (1987). https://doi.org/10.1007/BF00309759

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00309759

Key words

Navigation