Intrinsic innervation of the stomach of the fetal pig: an immunohistochemical study of VIP-immunoreactive nerve fibres and cell bodies

• Published in: Anatomia, histologia, embryologia Vol. 25; no. 4; p. 269
• Main Authors: van Ginneken, C, Weyns, A, van Meir, F, Ooms, L, Verhofstad, A
• Format: Journal Article
• Language: English
• Published: Germany 01.12.1996
• Subjects: Animals; Disease Models, Animal; Fetus - innervation; Immunohistochemistry - methods; Nerve Fibers - chemistry; Nerve Fibers - ultrastructure; Neurons - chemistry; Neurons - ultrastructure; Stomach - embryology; Stomach - innervation; Stomach Ulcer - physiopathology; Stomach Ulcer - veterinary; Swine - metabolism; Swine Diseases - physiopathology; Vasoactive Intestinal Peptide - analysis; Vasoactive Intestinal Peptide - physiology
• ISSN: 0340-2096
• DOI: 10.1111/j.1439-0264.1996.tb00091.x

Using an immunohistochemical technique, the presence and distribution of vasoactive intestinal polypeptide (VIP) was investigated in cryostat sections, both tangential and transverse, of the fetal pig's stomach. In all fetuses and in all gastric segments investigated, VIP-like immunoreactive (IR) nerve-cell bodies were seen in all intramural ganglia, and VIP-IR nerve fibres were found in all layers of the gastric wall except the tunica serosa. Consequently, VIP-IR nerve fibres were found to form a periglandular network, to accompany arterioles, to interconnect the intramural ganglia, to encircle both VIP-IR-negative and -positive neurons, and were found in all muscle layers. Despite the fact that VIP-IR seems to be restricted to the intramural nervous elements, some non-specific-reacting VIP-IR glandular cells were noticed in the basal parts of the fundic, antral and pyloric gastric glands. The distribution pattern of VIP in the fetal pig resembles that of the adult pig. This suggests a possible functional role for VIP during fetal life and/or puts forward the suggestion that the stomach of a fetal pig from the second half of the gestation period is prepared, from then on, for postnatal function. High similarities with regard to the general distribution pattern of VIP in the stomach have also been noted between the fetal pig and humans, proving once more that the fetal pig can serve as a good animal model in several research areas. Finally, the morphological data provided here may, combined with the physiological significance of VIP, contribute to a better insight into the physiopathology of economically important gastro-intestinal disorders in the pig, such as gastric ulceration.