Unique blood vasculature and innervation in the cavernous tissue of murine vomeronasal organs.

The vomeronasal organ (VNO) is an accessory olfactory device related to reproductive behavior. The soft tissue of the tubular organ is composed of sensory/non-sensory epithelia and a highly developed vasculature, which in the latter the dilation and contraction of blood vessels are thought to contribute to pumping in and out luminal fluid or air, like penile erectile tissue. The present histological observation of the murine VNO revealed a more complicated vasculature than previously evaluated ones with large differences along the rostro-caudal axis. An immunohistochemical study for vasoactive substances displayed extremely dense innervation by cholinergic nerves containing nitric oxide synthase and VIP/PHI in the thick smooth muscle layer surrounding venous sinuses at light and electron microscopic levels. Furthermore, the differential distribution of cholinergic nerves and adrenergic nerves may provide a novel insight into the pumping mechanism of VNO.

Histological features of the vomeronasal organ in the giraffe, Giraffa camelopardalis.

The vomeronasal organ (VNO) that preferentially detects species-specific substances is diverse among animal species, and its morphological properties seem to reflect the ecological features of animals. This histological study of two female reticulated giraffes (Giraffa camelopardalis reticulata) found that the VNO is developed in giraffes. The lateral and medial regions of the vomeronasal lumen were covered with sensory and nonsensory epithelia, respectively. The vomeronasal glands were positive for periodic acid-Schiff and alcian blue (pH 2.5) stains. The VNO comprises several large veins like others in the order Cetartiodactyla, suggesting that these veins function in a pumping mechanism in this order. In addition, numerous thin-walled vessels located immediately beneath the epithelia covering the lumen entirely surrounded the vomeronasal lumen. This sponge-like structure might function as a specific secondary pump in giraffes.

Anatomical, immnunohistochemical and physiological characteristics of the vomeronasal vessels in cows and their possible role in vomeronasal reception.

The general morphology of the vomeronasal vessels in adult cows was studied following a classic protocol, including optical, confocal and ultrastructural approaches. This anatomical work was completed immunohistochemically. The vomeronasal organ in cows is well developed, and its vessels are considerable in size. This fact allowed some functional properties of the vomeronasal arteries to be evaluated and, for the first time, their isometric tension to be recorded. Our functional studies were in agreement with the immunohistochemistry, and both corroborated the morphological data on the similarity between the vomeronasal vessels and those of the typical erectile tissue. In consequence, the vasoconstriction and vasodilation of the vomeronasal vessels would facilitate an influx and outflow of fluids in the vomeronasal organ, that is to say, this organ in cows would be able to work as a pump mechanism to send chemical signals to the vomeronasal receptor neurones.

The vomeronasal organ of the tammar wallaby.

The vomeronasal organ is the primary olfactory organ that detects sexual pheromones in mammals. We investigated the anatomy of the vomeronasal organ of the tammar wallaby (Macropus eugenii), a small macropodid marsupial. Pheromones may be important for activation of the hypothalamo-pituitary axis of tammar males at the start of the breeding season because plasma testosterone and luteinizing hormone concentration in males rise concurrently with pregnancy and the post-partum ovulation in females. The gross anatomy and the connection to the brain of the vomeronasal organ were examined by light and electron microscopy in adult male and female tammars. The vomeronasal organ was well developed in both sexes. The vomeronasal organ is a tubular organ connected at the rostral end via the nasopalatine duct (incisive duct) to the mouth and nasal cavity. At the rostral end the lumen of the vomeronasal organ was crescent shaped, changing to a narrow oval shape caudally. Glandular tissue associated with the vomeronasal organ increased towards the blind end of the organ. The tammar has the typical pattern of mammalian vomeronasal organs with electron-dense supporting cells and electron-lucent receptor cells. Microvilli were present on the surface of both epithelia while cilia were only found on the surface of the non-receptor epithelium. Some non-receptor epithelial cells appeared to secrete mucus into the vomeronasal organ lumen. The vomeronasal organ shows a high degree of structural conservation compared with eutherian mammals. The degree of vomeronasal organ development makes it likely that, as in other mammals, pheromones are important in the reproduction of the tammar.

Innervation of blood vessels in the vomeronasal complex of the rat.

We have made an immunohistochemical study of the vomeronasal (VN) complex of 12-day-old rats to characterize the innervation of its blood vessels. The VN complex can be subdivided into rostral, middle and caudal segments, each one with a particular vascularization pattern. Several small vessels were associated with the rostral segment, whereas a large venous sinus ran along the middle and caudal segments. Immunostaining for alpha-smooth muscle actin demonstrated that the muscular sheath was asymmetric, with more cells layers in its lateral than in its medial walls. Nerves were demonstrated with antisera against protein gene product 9.5 (PGP), and against several molecules associated with specific classes of nerve fibers: the C-terminal peptide of neuropeptide Y (CPON), calcitonin gene-related peptide (CGRP), substance P (SP), galanin (GAL), vasoactive intestinal peptide (VIP) and neuronal nitric oxide synthase (NOS). The latter, was also studied with NADPH-diaphorase. Vascular associated fibers exhibited NOS-, CPON-, GAL-, CGRP-, SP- and VIP-immunoreactivity. Only the vessels of the rostral segment showed VIP-immunoreactive fibers. Each wall of the venous sinus exhibited different types of nerve fibers. CPON-, GAL-, CGRP- and SP-immunoreactive fibers concentrated in the medial wall, whereas NOS-immunoreactive ones concentrated in the lateral wall. This distribution of vascular fibers, plus the presence of sensory fibers exhibiting CGRP-, SP- and GAL-immunoreactivity within the pseudostratified epithelium of the VN tube, would be relevant to understand the operation of the pumping mechanism regulating influx and efflux from the VN tube.

Supporting tissue and vasculature of the mammalian vomeronasal organ: the rat as a model.

The blood supply and osseocartilaginous support structures of the vomeronasal organ of the rat were studied. The study focused on adults, though 3- to 18-day-old animals were also examined. The techniques used included dissection and microdissection, injection of the vascular system with Araldite or with Indian ink in agar or gelatine, conventional histology, and scanning and transmission electron microscopy. The results indicated that blood reaches the vomeronasal organ via a branch of the sphenopalatine artery, and drains into an associated vein. Within the organ, one vein stood out by virtue of its size; this vein is accompanied by lesser veins, together with arterioles, capillaries, and lymphatic vessels. Connective tissue was readily apparent, though its distribution was heterogeneous. Analysis of series of transverse sections indicates that, in adults, the capsule that encases the vomeronasal organ is bony; in younger animals, the capsule is bony externally and cartilaginous internally; in very young animals, the capsule is entirely cartilaginous. However, it was noted that the change from cartilage to bone was due not to ossification of the existing cartilage, but to physical displacement of that cartilage by an extension of the vomer and incisive bones. Taken together, these results confirm the importance of considering the morphology of the vomeronasal organ as a whole, since there are major changes from rostral to caudal ends. Secondly, our findings regarding blood supply and the nature of the capsule support the view that the vomeronasal organ acts as a pump.

Origin and regional distribution of the arterial vessels of the vomeronasal organ in the sheep. A methodological investigation with scanning electron microscopy and cutting-grinding technique.

The origin and location of the arteries of the vomeronasal organ (VNO) in the sheep were studied by means of dissection, scanning electron microscopy of corrosion casts, and the cutting-grinding technique after injection with Araldite CY23-HY2967 via one of the carotid arteries. Dissection revealed that the most ventral of the three main branches of the sphenopalatine artery is responsible for the blood supply to the VNO. Scanning electron microscopy of corrosion casts revealed that the arterioles of the vomeronasal organ form a microvascular network. Cross sections of the region of the nasal cavity containing the VNO, obtained by the cutting-grinding technique, showed that the arterioles of the vomeronasal plexus are located medial and ventral to the vomeronasal duct. These results confirm the usefulness of the cutting-grinding technique as a complementary procedure in morphological studies of structures containing hard tissues.

The soft-tissue components of the vomeronasal organ in pigs, cows and horses.

The soft-tissue components of the vomeronasal organ of the pig, the cow and the horse were studied with the aid of dissection, microdissection, and light microscopy and immunohistochemistry of series of transverse sections. In horses, the rostral end of the incisive duct was blind: thus, unlike in pigs and cows, there was no communication between the vomeronasal organ and the oral cavity. In all three species, the central part of the vomeronasal duct bore the 'typical' respiratory/ receptor epithelium lining on its lateral and medical walls. The rostral part of the duct was characterized by stratified columnar epithelium, while more caudal parts bore simple columnar type. The patterns of distribution of glands, blood vessels and nerves were closely associated with the patterns of distribution of duct linings. The distribution of soft-tissue components in pigs was less clearly defined than in cows and horses. Of the three species, nerves were detected in the rostral half of the vomeronasal parenchyma only in the horse.

Distribution of the arterial supply to the vomeronasal organ in the cat.

BACKGROUND: The main goal of this work was to investigate the general distribution of arterial blood around and inside the vomeronasal organ (VNO) of the cat. METHODS: Macro- and microdissection methods together with light and scanning electron microscopy were used. Heads were injected with an India ink/agar mixture (the VNO subsequently being cut in transverse, sagittal and horizontal sections), with clear latex (the VNO subsequently being cut in transverse sections), or with an epoxy resin to obtain casts for examination by scanning electron microscopy. RESULTS: Dissection and microdissection show that the infraorbital, minor palatine, and descending palatine arteries have a common origin, rostral to the Rete mirabile arteria maxillaris. In transverse series and in the rostral half of the VNO, an arteriole is consistently observed between the vomeronasal duct and the lateral sheet of the vomeronasal cartilage. In this same segment, arterial branches with different orientations (perpendicular, horizontal, or transverse with respect to the main axis of the organ) are observed. Scanning electron microscopy of arterial casts shows that arterial vessels of the mucosa of the nasal septum have a direct relationship with the VNO. CONCLUSIONS: Branches of the sphenopalatine artery are the chief route of blood supply to the VNO. The vomeronasal parenchyma has few arterial vessels, and these are usually situated in the same position. Differences observed between the arteries inside and outside the VNO and the dilation of both by isoproterenol support the idea that the VNO is similar to erectile tissue organs and that it may act as a physiological pump.