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1.
Ethiop J Health Sci ; 30(3): 387-396, 2020 May.
Article in English | MEDLINE | ID: mdl-32874082

ABSTRACT

BACKGROUND: It has been documented that cardiac musculature is present in both venae cavae, and they contract together with the atrium, contributing to the pumping mechanism of the heart. So, in the present study, we measured the relative thicknesses of the three histological layers at formation, termination and intermediate levels of the venae cavae along with their histological characteristics. MATERIALS AND METHODS: Ten foetal and 10 adult cadavers were used. The Superior and Inferior Venae Cavae from all three regions were excised and processed for histology. The qualitative and quantitative features of the vessels were observed and recorded. The data thus obtained was then assessed statistically. RESULTS: In superior vena cava, the tunica intima grows actively especially during late gestation. The tunica media shows active growth. The tunica adventitia growth is significant at the middle and termination levels. In inferior vena cava, the tunica intima grows actively at the level of formation. The tunica media shows the active overall growth during early gestation. The tunica adventitia shows active growth during late gestation. In qualitative analysis the plump, spindle-shaped primitive mesenchymal cells were observed. Muscle and collagen fibers show reciprocal abundance with increasing age, with the former being lesser in amount than the latter in earlier stages. Appearance of vasa vasorum was notable from 2nd trimester. The cardiac myocytes were located in the middle and outer tunics of the superior vena cava. CONCLUSION: Cardiac musculature was absent in the inferior vena; however, the vessel shows advanced rate of overall development.


Subject(s)
Fetus/blood supply , Vena Cava, Inferior/growth & development , Vena Cava, Superior/growth & development , Venae Cavae/growth & development , Adult , Cadaver , Heart/anatomy & histology , Heart/growth & development , Humans , Vena Cava, Inferior/anatomy & histology , Vena Cava, Superior/anatomy & histology , Venae Cavae/anatomy & histology
2.
Elife ; 82019 02 08.
Article in English | MEDLINE | ID: mdl-30735130

ABSTRACT

Developing neurons of the peripheral nervous system reach their targets via cues that support directional growth, a process known as axon guidance. In investigating how sympathetic axons reach the heart in mice, we discovered that a combination of guidance cues are employed in sequence to refine axon outgrowth, a process we term second-order guidance. Specifically, endothelin-1 induces sympathetic neurons expressing the receptor Ednra to project to the vena cavae leading to the heart. Endothelin signaling in turn induces expression of the repulsive receptor Plexin-A4, via induction of the transcription factor MEF2C. In the absence of endothelin or plexin signaling, sympathetic neurons misproject to incorrect competing vascular trajectories (the dorsal aorta and intercostal arteries). The same anatomical and physiological consequences occur in Ednra+/-; Plxna4+/- double heterozygotes, genetically confirming functional interaction. Second-order axon guidance therefore multiplexes a smaller number of guidance cues in sequential fashion, allowing precise refinement of axon trajectories.


Subject(s)
Endothelins/genetics , Heart/growth & development , Nerve Tissue Proteins/genetics , Receptor, Endothelin A/genetics , Receptors, Cell Surface/genetics , Semaphorins/genetics , Animals , Arteries/growth & development , Arteries/metabolism , Axon Guidance/genetics , Axons/metabolism , Gene Expression Regulation, Developmental/genetics , Heterozygote , MEF2 Transcription Factors/genetics , Mice , Mice, Knockout , Neurogenesis/genetics , Neurons/metabolism , Signal Transduction/genetics , Sympathetic Nervous System/growth & development , Sympathetic Nervous System/metabolism , Venae Cavae/growth & development , Venae Cavae/metabolism
3.
Ann Vasc Surg ; 27(7): 947-53, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23993110

ABSTRACT

BACKGROUND: The latest generation in titanium clip application systems, the AnastoClip Vessel Closure System (VCS; LeMaitre Vascular, Burlington, MA), allows surgeons to perform vascular anastomosis more easily and faster than conventional sutures. This system may become the option of choice for vascular reconstruction in pediatric surgery where, as in the case transplant surgery, decreasing vascular occlusion times may influence outcome. The aim of this study was to determine whether VCS metallic clips would allow shorter anastomosis times than conventional interrupted polypropylene or running polyglycolic acid suturing in end-to-end anastomosis performed in the abdominal cava of young pigs. METHODS: Thirty-two domestic swine, 45 days old, were used for this study. All animals were subjected to an end-to-end anastomosis in the abdominal cava. RESULTS: VCS clips are easier to use for the surgeon, significantly decreasing cross-clamping time in caval anastomosis (VCS 10.33 ± 1.75 min vs. interrupted polypropylene sutures 46.00 ± 6.16 min vs. continuous polyglycolic acid sutures 18.16 ± 1.47 min). CONCLUSIONS: VCS clips significantly decrease the time needed for performing an end-to-end anastomosis in the abdominal cava, decreasing cross-clamping time when compared to interrupted polypropylene or running polyglycolic acid sutures.


Subject(s)
Absorbable Implants , Metals , Surgical Instruments , Suture Techniques/instrumentation , Sutures , Vascular Surgical Procedures/instrumentation , Venae Cavae/surgery , Age Factors , Anastomosis, Surgical , Animals , Constriction , Equipment Design , Male , Models, Animal , Polyglycolic Acid , Polypropylenes , Sus scrofa , Suture Techniques/adverse effects , Task Performance and Analysis , Time Factors , Vascular Surgical Procedures/adverse effects , Venae Cavae/growth & development
4.
J Pediatr Surg ; 47(7): 1390-8, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22813802

ABSTRACT

BACKGROUND/PURPOSE: Our aim was to perform a macroscopic and imaging (ultrasonographic and angiographic) evaluation of vascular closure stapler (VCS) metallic clips for renal transplantation in growing piglets to assess their role for transplantation surgery in young children. If these techniques are to be useful, it is necessary to prove that their use avoids one of the main pitfalls of conventional sutures in this setting, namely lack of growth in the suture line. METHODS: Twenty-four piglets were used for this study. Animals were subjected to a heterotopic renal autotransplantation when they were 45 days old. The right kidney was moved from its normal location to the cranial area of the iliac fossa. The end-to-side anastomoses between the renal artery and vein and the aorta and vena cava, respectively, were performed using VCS metallic clips in 6 animals. Continuous polypropylene suturing was used in another 6 piglets, and continuous polyglycolic acid suture was used in 6 additional piglets. A control group of 6 animals without renal autotransplantation was also included in the study. All animals were allowed to grow for 6 months, during which time serial angiographic and ultrasonographic studies were carried out to assess the existence of vascular flow disturbances or stenosis. Similarly, angiographic measurements were obtained to document growth at the anastomotic site. Longitudinal growth was evaluated postmortem after the 6-month growing period. RESULTS: Angiography showed significant (P < .001) transverse growth in both arteries and veins belonging to the VCS clips, running absorbable suture, or control groups. No significant difference was observed among the 3 groups. Vascular growth in the running nonabsorbable suture (polypropylene) group, however, was significantly less than in the other 3 groups and did not significantly differ from baseline. Baseline luminal diameters at the anastomotic site as measured by angiography in the VCS group were 3.64 ± 0.40 mm in the artery and 5.30 ± 1.43 mm in the vein. After growth, these values increased to 6.87 ± 0.90 mm and 11.27 ± 2.53 mm, respectively. Significant longitudinal growth was evidenced macroscopically after 6 months in both aorta and vena cava in all groups. On the other hand, significant longitudinal growth in the renal artery and vein were only observed in the control, VCS, and absorbable suture groups. CONCLUSIONS: In this experimental setting, satisfactory macroscopic and angiographic vascular growth results were obtained using the VCS clips, suggesting that this suture could be the technique of choice in pediatric transplantation surgery.


Subject(s)
Aorta/surgery , Kidney Transplantation/methods , Renal Artery/surgery , Renal Veins/surgery , Surgical Stapling/instrumentation , Transplantation, Heterotopic/methods , Venae Cavae/surgery , Anastomosis, Surgical/instrumentation , Anastomosis, Surgical/methods , Animals , Aorta/diagnostic imaging , Aorta/growth & development , Aortography , Male , Renal Artery/diagnostic imaging , Renal Artery/growth & development , Renal Veins/diagnostic imaging , Renal Veins/growth & development , Surgical Stapling/methods , Suture Techniques/instrumentation , Sutures , Swine , Ultrasonography , Venae Cavae/diagnostic imaging , Venae Cavae/growth & development
5.
Morfologiia ; 126(5): 30-3, 2004.
Article in Russian | MEDLINE | ID: mdl-15847292

ABSTRACT

Using light and electron microscopic methods, the histogenesis and structural organization of the walls of rat venae cavae and pulmonary veins were studied in prenatal and postnatal periods of development. The special attention was paid to the appearance of the striated myocytes in the walls of these vessels during the process of ontogenesis. The time of initial divergent development of myoblastic differon was established, the stages of differentiation of striated myoblasts and the peculiarities of intercellular junctions were characterized, as well as the innervation and vascularization of the walls of venae cavae and pulmonary veins.


Subject(s)
Organogenesis , Pulmonary Veins/embryology , Pulmonary Veins/growth & development , Venae Cavae/embryology , Venae Cavae/growth & development , Animals , Cell Differentiation , Muscle Cells/cytology , Muscle Fibers, Skeletal/cytology , Pulmonary Veins/cytology , Rats , Venae Cavae/cytology
6.
Cytokine ; 8(9): 675-85, 1996 Sep.
Article in English | MEDLINE | ID: mdl-8932978

ABSTRACT

The expression of transforming growth factor beta 1 and beta 2 (TGF-beta 1 and beta 2) in aortic and venous tissue from male New Zealand White rabbits, at selected time intervals after birth, was examined by the reverse transcriptase polymerase chain reaction. Stable levels of TGF-beta 1 were found in all segments derived from the aortic arch and descending aorta at each time interval. However, increasing amounts of TGF-beta 2 transcripts were observed for the aortic arch from day 4, with peaks occurring between 1 and 6 months of age, followed by progressively decreasing levels thereafter. TGF-beta 2 transcripts in the descending aorta generally did not change significantly over time. TGF-beta transcripts manifested a significantly lower expression in the vena cava than in aortic segments. Histological analysis of the vascular tissue showed cellular hyperplasia (2.5-fold greater prevalence of nuclei per field) in the aortic arch media at 1 month of age as compared with nuclei per field at 12 months and increasing thickness of the aortic arch media with time. No significant differences in relative collagen concentrations were observed among the aortic and vena cava segments. These results suggest that these TGF-beta isoforms may participate in the physiological induction and differentiation of arterial and venous tissue during early normal vascular maturation.


Subject(s)
Endothelium, Vascular/metabolism , Transforming Growth Factor beta/biosynthesis , Actins/biosynthesis , Animals , Aorta, Thoracic/cytology , Aorta, Thoracic/growth & development , Aorta, Thoracic/metabolism , Blotting, Northern , Endothelium, Vascular/cytology , Hyperplasia , Male , Oligonucleotide Probes , Polymerase Chain Reaction , RNA/biosynthesis , Rabbits , Transcription, Genetic , Venae Cavae/cytology , Venae Cavae/growth & development , Venae Cavae/metabolism
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