The lymphatic drainage of the peritoneal cavity with reference to the treatment of ascites by lympho-venous shunt

1976 ◽  
Vol 32 (7) ◽  
pp. 826-827 ◽  
Author(s):  
G. Szabó
1960 ◽  
Vol 199 (6) ◽  
pp. 1021-1024 ◽  
Author(s):  
Harry E. Raybuck ◽  
Lane Allen ◽  
W. S. Harms

The subserous lymphatic plexus on the peritoneal surface of the diaphragm was obliterated to study the removal of protein from the peritoneal cavity in the absence of lymphatic drainage. Cats weighing between 2 and 3 kg were used for this study. Homologous and heterologous serum was injected into the peritoneal cavity of lightly anesthetized animals. In control animals the absorption of 50 ml of homologous serum was complete in 9 hours, and absorption of 50 ml of heterologous serum required 24–36 hours. Cats in which lymphatic peritoneal drainage had been experimentally obstructed showed an increase in time interval for absorption of injection serums. Under this condition 144 hours was required for absorption of heterologous serum and 72 hours for homologous serum.


1993 ◽  
Vol 13 (4) ◽  
pp. 270-279 ◽  
Author(s):  
Lisa Tran ◽  
Helen Rodela ◽  
John B. Hay ◽  
Dimitrios Oreopoulos ◽  
Miles G. Johnston

Objective It has been suggested that lymphatics may contribute to ultrafiltration failure in patients on continuous ambulatory peritoneal dialysis (CAPD) byabsorbing dialysate and ultrafiltrate from the peritoneal cavity. In most studies lymphatic drainage has been estimated from the disappearance of an instilled tracer from the peritoneal cavity or estimated from the appearance of an intraperitoneally administered tracer in the bloodstream. However, in sheep it is possible to cannulate several of the relevant lymphatics that drain the peritoneal cavity and assess lymph drainage parameters directly. The purpose of this study was to estimate lymph drainage from the peritoneal cavity in sheep using the disappearance of tracer from the cavity and the appearance of intraperitoneally instilled tracer in the bloodstream and to compare these results with those obtained from our previous studies using cannulation techniques. Design Experiments were performed in anesthetized and nonanesthetized animals. Volumes of 50 mL/kg of Dianeal 4.25% containing 25 μCi of 1251-albumin were infused into the peritoneal cavity. Results In anesthetized sheep the calculated peritoneal lymph drainage from monitoring the disappearance of tracer from the peritoneal cavity over 6 hours was 1.873±0.364 mL/kg/hour. Monitoring the appearance of tracer in the blood gave significantly lower peritoneal lymph flow rates of 1.094±0.241 mL/kg/hour. Directly measured lymph flow rates from our earlier publication were lower still and ranged from 0.156±0.028 -0.265±0.049 mL/hour/kg, depending on how we estimated the right lymph duct contribution to peritoneal drainage, since we could not cannulate this vessel. We repeated these experiments in conscious sheep. The value for lymph flow estimated from the disappearance of tracer from the peritoneal cavity was 2.398±0.617 mL/hour/kg and from the appearance of tracer in the blood, 1.424±0.113 mL/ hour/kg. The1ymph flow rates monitored from indwelling lymphatic catheters ranged from 1.021 ±0.186 -1.523±0.213 mL/hour/kg (again, depending on our estimates for the right lymph duct). Conclusions Lymph flow rates measured from indwelling lymphatic catheters provided the most conservative values for lymphatic drainage of the peritoneal cavity under dialysis conditions. Estimates of lymphatic drainage based on the appearance of tracer in the blood gave values that were on average higher. The method using the disappearance of tracer from the cavity to estimate lymph flows overestimated peritoneal lymph drainage. Fluid was lost from the peritoneal cavity, and the estimated proportion of liquid lost through lymphatic drainage depended on the technique used to measure lymph flow rates.


1993 ◽  
Vol 74 (2) ◽  
pp. 859-867 ◽  
Author(s):  
L. Tran ◽  
H. Rodela ◽  
N. J. Abernethy ◽  
Z. Y. Yuan ◽  
J. B. Hay ◽  
...  

Lymphatic drainage of the peritoneal cavity may reduce ultrafiltration in continuous ambulatory peritoneal dialysis. We assessed lymphatic drainage of the peritoneal cavity in sheep under dialysis conditions by cannulation of the relevant lymphatic vessels and compared lymphatic drainage in anesthetized and conscious animals. Lymph was collected from the caudal mediastinal lymph node and the thoracic duct, both of which are involved in the lymphatic drainage of the ovine peritoneal cavity. Volumes of a hypertonic dialysis solution (50 ml/kg 4.25% Dianeal) containing 25 microCi 125I-human serum albumin were instilled into the peritoneal cavity, and lymph flows and the appearance of labeled protein in the lymphatic and vascular compartments were monitored for 6 h. Intraperitoneal pressures increased 4–5 cmH2O above resting levels after infusion of dialysate. On the basis of the appearance of tracer in the lymph, drainage of peritoneal fluid into the caudal lymphatic was calculated to be 3.09 +/- 0.69 and 14.14 +/- 2.86 ml/h in anesthetized and conscious sheep, respectively. Drainage of peritoneal fluid into the thoracic duct preparations was calculated to be 1.32 +/- 0.33 and 14.69 +/- 5.73 ml/h in anesthetized and conscious sheep, respectively. Significant radioactivity was found in the bloodstream, and at least a portion of this was likely contributed by the right lymph duct, which was not cannulated in our experiments.(ABSTRACT TRUNCATED AT 250 WORDS)


1986 ◽  
Vol 6 (3) ◽  
pp. 113-121 ◽  
Author(s):  
Ramesh Khanna ◽  
Robert Mactier ◽  
Zbylut J. Twardowski ◽  
Karl D. Nolph

Lymphatic drainage of particulate matters from the peritoneal cavity occurs mainly from lacunae located in the diaphragm. These are a triple-layered structure consisting of mesothelium, a loose network of connective tissue and endothelium. Absorption of particles may occur via gap junctions, through the cells or via vesicles. Whole blood can be removed fairly rapidly from the peritoneal cavity. Respiration plays an important role in the absorption of particles through lymphatics. Intra-abdominal pressure and posture are other factors which influence lymphatic flow rate in the peritoneal cavity. Little is known about the influence of drugs on lymphatic flow rate from the peritoneal cavity.


1989 ◽  
Vol 9 (2) ◽  
pp. 85-90 ◽  
Author(s):  
Andrzej Breborowicz ◽  
Helen Rodela ◽  
D.G. Oreopoulos

Peritoneallymphatic flow in normal and uremic rabbits was measured by estimation of the disappearance of the radiolabelled 1311–albumin from the peritoneal cavity. The results show that lymph flow rate from the peritoneal cavity is not steady and depends on dialysate volume, its tonicity, and protein content. During peritoneal dialysis, peritoneal lymphatic flow is lower at the beginning of an exchange. Peritoneal lymphatic drainage is higher in uremic rabbits compared to normal controls.


1991 ◽  
Vol 260 (3) ◽  
pp. F353-F358 ◽  
Author(s):  
N. J. Abernethy ◽  
W. Chin ◽  
J. B. Hay ◽  
H. Rodela ◽  
D. Oreopoulos ◽  
...  

Lymphatic drainage of the peritoneal cavity has been investigated in anesthetized sheep. Studies involving intraperitoneal administration of a complex of Evans blue dye and bovine serum albumin demonstrated the existence of three anatomically distinct pathways. In the first pathway, dye is removed from the peritoneal cavity by diaphragmatic lymphatics that pass into caudal sternal lymph nodes. Efferent lymphatics from these nodes transport the material to cranial sternal lymph nodes. Efferent cranial sternal lymphatics then convey the material either directly or indirectly, via tracheal lymphatic trunks, to the right lymph duct. In the second pathway, the complex is transported from the peritoneal cavity by diaphragmatic lymphatics that pass into the caudal mediastinal lymph node. Efferent lymphatic ducts from this node transport the material to the thoracic duct. The third pathway appears to involve transport of the dye across the mesothelial lining of the abdominal viscera and removal from the interstitium by afferent visceral lymphatics. Material taken up in this manner is ultimately transported to the thoracic duct by efferent visceral lymphatics. Experiments involving measurements of lymphatic absorption of 125I-labeled human serum albumin from the peritoneal cavity indicated that, over the 6-h period studied, 4.55 +/- 1.20 and 1.43 +/- 0.56% of the injected tracer could be recovered in thoracic duct lymph and caudal mediastinal efferent lymph, respectively, and the sum of these values represented 26% of the recovered radioactivity. On the other hand, 16.95 +/- 6.93% of the injected radioactivity could be found in the blood over the same period.(ABSTRACT TRUNCATED AT 250 WORDS)


1996 ◽  
Vol 16 (2) ◽  
pp. 163-171 ◽  
Author(s):  
Helen Rodela ◽  
Zheng-Yi Yuan ◽  
John B. Hay ◽  
Dimitrios G. Oreopoulos ◽  
Miles G. Johnston

Objectives The purpose of this study was to investigate the effects of acute peritonitis on lymphatic drainage of the peritoneal cavity in conscious sheep Design Peritonitis was induced with the addition of 1% casein or 1% albumin to the dialysis solution. Thirty sheep (5 groups of 6) were used in this study. One group received 50 mL/kg intraperitoneal infusions of Dianeal 4.25% (486 mOsm/L); a second group received 1% casein-DianeaI4.25% (493 mOsm/L); a third group received 1% albumin-Dianeal 4.25% (487 mOsm/L). In the fourth and fifth groups (controls and casein-injected) lymph was collected from the caudal mediastinal lymph node and the thoracic duct, both of which are involved in the lymphatic drainage of the peritoneal cavity (peritonitis induced with casein). 1251-human serum albumin (25 μCi) was added to the dialysate as the lymph flow marker. Lymph drainage was estimated from (1) the appearance of the intraperitoneally administered tracer in the blood; (2) the disappearance of the tracer from the peritoneal cavity; and (3) the recovery of tracer in lymph. Results In noncannulated animals the cumulative volume removed by lymphatics over 6 hours (based on tracer recovery in blood) was 10.5 ±1.0 mL/kg in control animals versus 5.0 ± 0.6 mL/kg and 8.6 ± 1.2 mL/kg in casein and albumin-infused sheep, respectively. The suggestion of decreased lymph drainage in peritonitis was supported by the cannulation experiments. While the cumulative fluid removed from the peritoneal cavity over 6 hours in caudal lymph was unaffected by peritonitis (3.8 ± 0.4 mL/kg in controls vs 3.6 ± 0.5 mL/kg in casein injected animals), peritonitis reduced flow into the thoracic duct from 3.0 ± 0.3 to 1.1 ± 0.3 mL/kg. The sum of the volume removed in lymph in the cannulated preparations was 6.8 ± 0.4 mL/kg in controls versus 4.7 ± 0.5 mL/kg in the peritonitis group. The total volume removed from the cavity (including an estimate of flow based on the residual recovery of tracer in blood) was reduced from 12.6 ±1.4 in controls to 7.8 ± 0.6 mL/kg in the peritonitis sheep. In contrast, estimates of lymph drainage based on the disappearance of tracer from the peritoneal cavity suggested that lymph drainage increased (from 16.6 ±1.6 mL/kg in controls to 17.8 ±1.5 mL/kg and 25.5 ±1.7 mL/kg in the casein and albumin groups, respectively, in noncannulated animals and from 15.3 ± 1.4 mL/kg in controls to 25.0 ± 1.7 mL/kg in the cannulated group). In both noncannulated and cannulated sheep the total recovery of tracer was less in the peritonitis groups. Conclusions These studies demonstrated that lymph drainage of the peritoneal space was decreased in a casein peritonitis model. The decrease in lymph drainage is most obvious in the visceral pathway leading to the thoracic duct; however, diaphragmatic drainage into the right lymph duct may also be inhibited. The disappearance of tracer from the peritoneal cavity was elevated during peritonitis. Tracer disappearance has been used to estimate lymph drainage, but this approach suggested, incorrectly, that lymph flow had increased.


1992 ◽  
Vol 26 (3) ◽  
pp. 200-205 ◽  
Author(s):  
A. J. Marco ◽  
M. Domingo ◽  
J. Ruberte ◽  
A. Carretero ◽  
V. Briones ◽  
...  

The lymphatic drainage of the peritoneal cavity has been investigated by intraperitoneal inoculation of an intracellular bacterium ( Listeria monocytogenes) and an inert marker (Indian ink). The results reveal that both agents are transported, either after phagocytosis by intraperitoneal macro phages or in suspension in the lymph, towards the cranial sternal lymph nodes ( Lymphonodi sternales craniales) of the ventral thoracic Iymphocentrum ( Lymphocentrum thoracicum ventrale) and to the lymph nodes of the mediastinal lymphocentrum ( Lymphocentrum mediastinale), prior to systemic dissemination. This mechanism of peritoneal lymph drainage has relevance on experimental studies involving the inoculation of pathogens, and on the investigation of metastatic diffusion of neoplasms from the peritoneum.


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