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Biomedical subjects

W P Duguid

Publications and source records attributed to W P Duguid.

At least 37 records · Page 2Linked to original sources

Expression of endothelin-1 in the lungs of patients with pulmonary hypertension.

BACKGROUND: Pulmonary hypertension is characterized by an increase in vascular tone or an abnormal proliferation of muscle cells in the walls of small pulmonary arteries. Endothelin-1 is a potent endothelium-derived vasoconstrictor peptide with important mitogenic properties. It has therefore been suggested that endothelin-1 may contribute to increases in pulmonary arterial tone or smooth-muscle proliferation in patients with pulmonary hypertension. We studied the sites and magnitude of endothelin-1 production in the lungs of patients with various causes of pulmonary hypertension. METHODS: We studied the distribution of endothelin-1-like immunoreactivity (by immunocytochemical analysis) and endothelin-1 messenger RNA (by in situ hybridization) in lung specimens from 15 control subjects, 11 patients with plexogenic pulmonary arteriopathy (grades 4 through 6), and 17 patients with secondary pulmonary hypertension and pulmonary arteriopathy of grades 1 through 3. RESULTS: In the controls, endothelin-1-like immunoreactivity was rarely seen in vascular endothelial cells. In the patients with pulmonary hypertension, endothelin-1-like immunoreactivity was abundant, predominantly in endothelial cells of pulmonary arteries with medial thickening and intimal fibrosis. Likewise, endothelin-1 messenger RNA was increased in the patients with pulmonary hypertension and was expressed primarily at sites of endothelin-1-like immunoreactivity. There was a strong correlation between the intensity of endothelin-1-like immunoreactivity and pulmonary vascular resistance in the patients with plexogenic pulmonary arteriopathy, but not in those with secondary pulmonary hypertension. CONCLUSIONS: Pulmonary hypertension is associated with the increased expression of endothelin-1 in vascular endothelial cells, suggesting that the local production of endothelin-1 may contribute to the vascular abnormalities associated with this disorder.

Adult↗

Neoplastic transformation of propagable cultured rat pancreatic duct epithelial cells by azaserine and streptozotocin.

The role of duct cells in the histogenesis of pancreatic carcinoma was studied using a propagable cultured pancreatic duct epithelial cell line derived from a Fischer-344 rat. Tumorigenic transformation was induced by treatment with two experimental pancreatic carcinogens, azaserine and streptozotocin, or spontaneously using a 'selective' culture condition. Tumors arising from spontaneously transformed cells were anaplastic carcinomas, while those from streptozotocin-transformed cells were well or moderately differentiated ductal adenocarcinomas. Azaserine-treated cells produced moderately to poorly differentiated adenocarcinomas. Ultrastructural evidence of acinar or endocrine differentiation was absent. The biochemical phenotypes of representative tumor cell lines established from these tumors were studied. As compared to the parental cell line which expressed high activity of carbonic anhydrase (CA) and negligible activity of gamma-glutamyl transpeptidase (GGT), the tumor cell lines displayed variably increased levels of GGT, and a diminution or loss of CA activity. The tumor cell lines also showed heterogeneity in proto-oncogene and growth factor/receptor expression. The transforming growth factor-alpha mRNA expression was increased in all tumor cell lines, especially in those induced by azaserine. In contrast, mRNA expression of epidermal growth factor receptor was markedly down-regulated in all tumor cell lines. All chemically induced tumor cell lines showed marked overexpression of the c-myc and c-Ki-ras mRNAs, whereas the spontaneously transformed tumor cell line showed only a significant overexpression of the c-Ki-ras. Point mutation of this proto-oncogene at codons 12, 13 or 61 was absent. The results show that azaserine and streptozotocin are potent carcinogens in vitro for cultured rat pancreatic duct epithelial cells, and the phenotype of the tumors is modulated by the method or agent used for their transformation.

Animals↗

Renal cell carcinoma presenting as nephrotic syndrome complicated by acute renal failure.

A case of minimal change nephropathy occurring in association with a renal cell carcinoma is presented and discussed. The case was unusual in that it was associated with acute renal failure necessitating hemodialysis for five weeks. The renal failure resolved but the nephrotic state persisted in spite of therapy with prednisone then cyclophosphamide. The literature on nephrotic syndrome causing acute renal failure and its association with solid tumors is briefly reviewed.

Acute Kidney Injury↗

Genotoxicity of pancreatic chemical carcinogens to propagable cultured normal pancreatic epithelial cells.

The cytotoxic and DNA-damaging effects of the pancreatic carcinogens azaserine, streptozotocin, and N-nitrosobis(2-oxyopropyl)amine (BOP) on propagable cultured normal rat pancreatic epithelial cells have been studied. All three chemicals in micromolar concentrations produced cytotoxicity to these cells. The concentrations that caused 50% reduction in colony formation (LD50) were approximately 0.3 mM for azaserine, 0.4 mM for BOP, and 2 mM for streptozotocin. Comparatively, the LD50 for N-methyl-N'-nitro-N-nitrosoguanidine was 3 microM. The toxicity of both azaserine and BOP did not require exogenously added S9 microsomal enzymes, indicating that the cells were capable of metabolic activation of these carcinogens. All three compounds induced unscheduled DNA synthesis, thus suggesting their mutagenic and carcinogenic potential in these cultured cells.

Animals↗

Adverse effects of cyclosporine on islet growth and differentiation.

In light of recent evidence that cyclosporine (CsA) inhibits growth of the exocrine pancreas, we decided to examine the effects of cyclosporine in a hamster model of islet cell proliferation and differentiation induced by partial pancreatic duct obstruction (PPDO), in which the growth of pancreatic endocrine tissue is mediated by production of an islet cell growth factor (ICGF) contained in a cytosolic extract of pancreas. In Part I of this study, extract was prepared from PPDO pancreas, from PPDO pancreas in animals treated with CsA (20 mg/kg ip daily for 10 days), and from pancreas in control animals. Data obtained from an in vivo bioassay confirmed that administration of the extract derived from PPDO and PPDO + CsA animals increased pancreatic organ weight significantly by 10 and 17%, respectively, compared to control. Similarly, total pancreatic DNA content was increased significantly by 25 and 41%, respectively. In Part II of the study, the direct effect of CsA on islet cell proliferation and differentiation induced by PPDO was examined. The number of islets per square millimeter and the uptake of tritiated thymidine by islet cells (%) were increased significantly in PPDO animals (2.4 +/- 0.1 and 0.56 +/- 0.06) compared to those in PPDO + CsA animals (1.2 +/- 0.1 and 0.24 +/- 0.01) and to those in controls (1.1 +/- 0.0 and 0.22 +/- 0.07). It is concluded from the data in Part I that CsA does not inhibit ICGF production, but the results of Part II suggest that CsA acts to block ICGF activity.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Trophic stimulation of the ductal/islet cell axis: a new approach to the treatment of diabetes.

The purpose of this study was to demonstrate that the pancreas of the hamster contains a growth factor(s) that can induce cells associated with the ductular epithelium to differentiate along an endocrine pathway and thereby provide a means of regenerating a functioning islet cell mass. We have shown previously that partial obstruction of the pancreatic duct leads to the induction of nesidioblastosis. A cytosol extract prepared from the partially obstructed hamster pancreas was injected at a dose of 4000 microliters intraperitoneally twice a day for 2 days and produced significant increases in pancreatic weight, protein, and deoxyribonucleic acid of 18%, 18% and 42% respectively, over saline-treated control animals. To assess the effects of this extract on morphology, 150 microliters intraperitoneally twice a day was administered for 21 days. Tissue was processed for histologic, morphometric, and autoradiographic analysis. Budding of endocrine cells from cells of the terminal ductules was observed in cytosol-injected animals and the number of islets per square millimeter was determined to be increased by 100% compared with saline-treated controls (p less than 0.01). Tritiated thymidine uptake by ductal and islet cells was increased tenfold and sixfold, respectively, over that of control animals (p less than 0.01). Cytosol extract was also administered to hamsters rendered diabetic by streptozocin. Survival in these animals was 100% compared with only 60% for saline-treated control animals (p less than 0.05). Furthermore, the blood levels of glucose in cytosol-treated animals was significantly less than the levels in saline-treated controls (p less than 0.05). We conclude that the pancreas does indeed contain a growth factor(s) responsible for the induction of nesidioblastosis and the new islet tissue is functionally capable of stabilizing a diabetic state.

Animals↗

The pancreas of Syrian golden hamsters. Age-related autoradiographic observations.

We examined the effects of aging on the uptake of tritiated thymidine (3H-TdR) by the different cell types of the pancreas of the Syrian golden hamster. Animals, 8-22-wk-old, received 3H-TdR (2 microCi/gm) intraperitoneally and were sacrificed 1 h later. Pancreatic tissue from each animal was processed for autoradiography. The percentage of acinar cells labeled with 3H-TdR was 1.17 +/- 0.26 at 8-wk-old and steadily diminished to 0.02 +/- 0.00 at 22 wk. The percentage of ductular and islet cells labeled with 3H-TdR at 8 wk was 0.24 +/- 0.24 and 0.16 +/- 0.01, respectively and at 22 wk was 0.13 +/- 0.09 and 0.18 +/- 0.01, respectively. In contrast with acinar cells, the percentage of ductular and islet cells labeled with 3H-TdR between 10- and 20-wk-old showed considerable variability. In the major ducts in the head of the gland, the number of epithelial cells per mm duct length labeled with 3H-TdR did not change throughout the study; 3.25 +/- 1.5 at 8 wk and 3.35 +/- 1.3 at 22 wk. It is concluded that acinar cell growth is an inverse function of age between 8-22 wk and that differentiated cell types in the pancreas of the Syrian golden hamster are capable of incorporating 3H-TdR during the S-phase of the cell cycle.

Aging↗

The effect of cellophane wrapping of the pancreas in the Syrian golden hamster: autoradiographic observations.

We examined the effects of cellophane wrapping of the pancreas on the age-related uptake of tritiated thymidine (3H-TdR) by the differentiated cell types of the pancreas of the Syrian golden hamster. Fifty-two hamsters were studied. At 7 weeks of age, hamsters underwent cellophane wrapping (n = 32) or were allocated to a control group (n = 20). Animals 8-22 weeks of age (four at each interval) received 3H-TdR (2 microCi/g) intraperitoneally and were killed 1 h later. Pancreatic tissues from each animal was processed for autoradiography. The percent of acinar cells labeled with 3H-TdR at 8 weeks, in control and wrapped animals, was 1.17 +/- 0.26 and 1.51 +/- 0.38 respectively (p = N.S.). In control animals, this steadily diminished to 0.02 +/- 0.00 at 22 weeks. In wrapped animals, there was less of a tendency for acinar cell labeling to decrease with age, and the percent of labeled acinar cells in wrapped animals at 22 weeks was 0.05 +/- 0.00. The percent of ductular cells labeled with 3H-TdR at 8 weeks in control and wrapped animals was 0.24 +/- 0.24 and 0.98 +/- 0.24, respectively (p = N.S.), and at 22 weeks was 0.13 +/- 0.90 and 0.60 +/- 0.03, respectively (p less than 0.01). The percent of islet cells labeled with 3H-TdR at 8 weeks in control and wrapped animals was 0.16 +/- 0.01 and 0.42 +/- 0.01, respectively (p less than 0.05), and at 22 weeks was 0.18 +/- 0.01 and 0.63 +/- 0.05 (p less than 0.05), respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Association of cholecystectomy with pancreatic growth and increased plasma levels of cholecystokinin in the Syrian golden hamster.

This study examined the effect of cholecystectomy on plasma concentrations of cholecystokinin (CCK) and pancreatic growth. Seventy female Syrian golden hamsters were used in the investigation. Half the animals underwent cholecystectomy and half had a sham procedure. Following cholecystectomy, significant increases were observed in pancreatic weight (11-41%), total DNA content (8-16%), total protein content (9-19%), DNA synthesis rate (57-200%), and in random plasma CCK concentrations (12-81%) in comparison to the control group. There was no significant change in protein synthesis rate. We conclude that cholecystectomy may have a significant trophic effect on the pancreas and that this effect may be mediated by an increase in circulating levels of CCK.

Animals↗

Induction of nesidioblastosis will reverse diabetes in Syrian golden hamster.

Nesidioblastosis, which is the formation of new islets and the differentiation of cells within the islets, represents part of the spectrum of hyperfunctioning states of the islets of Langerhans at the clinical level. Nesidioblastosis in the Syrian golden hamster can be induced by wrapping the head of the pancreas with cellophane tape. Ligation of the duct is not involved, and acinar cell atrophy does not occur. The purpose of this study was to determine whether the induction of nesidioblastosis could be used as a means of reversing streptozocin-induced diabetes. Outbred hamsters (n = 32), 8 wk of age, were rendered diabetic by treatment with 40 mg/kg i.p. streptozocin, administered daily for 3 days. Four days later, 16 animals chosen at random underwent laparotomy with cellophane wrapping of the pancreas. Before surgery, the serum glucose and insulin levels (means +/- SE) in the unoperated control animals (389.0 +/- 18.6, 33.9 +/- 3.8) did not differ from those in the animals awaiting the operation (373.2 +/- 18.6, 37.9 +/- 3.8). After 7 wk, 50% of the operated animals had serum glucose and insulin levels that were normal, compared to only 12% of the unoperated control animals (chi2 = 5.53, P less than .05). Islets from normoglycemic operated animals were characterized by increased numbers, including many small islets, positive immunoreactive insulin staining, and minimal vacuolation of cells. Islets from hyperglycemic operated hamsters and from the unoperated control animals were decreased in number and generally larger in size, demonstrated little or no immunoreactive insulin staining, and exhibited marked vacuolation of cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Establishment of propagable epithelial cell lines from normal adult rat pancreas.

A method for establishing propagable epithelial cell lines from normal adult rat pancreas is described. Morphological studies showed that these cells were derived from duct epithelial cells. These cells grew equally well in media containing fetal bovine (FBS) or horse serum (HS). Preliminary studies suggested that propagable cultured pancreatic ductal cells during early passages retained some capacity to differentiate into acinar-like cells with the formation of granules resembling zymogen, especially when these cells were cultured on mixed ester cellulose membrane. This supports the concept that pancreatic ductal lining cells represent the 'stem' cells on pancreatic epithelial cells. Propagable pancreatic epithelial cells in long-term cultures will be useful in the histogenetic and mechanistic studies of pancreatic carcinogenesis.

Animals↗

Neurotropic malignant melanoma of right temple with orbital metastasis: a clinicopathological case report.

A case is reported of neurotropic melanoma developed from a superficial spreading melanoma with minimal cytological deviation, situated in the right temple. The nine-year course was clinically characterised by local recurrences, involvement of the orbit and the parotid region via neurogenic invasion, and systemic metastases to lung, seventh rib, and the brain. The histopathology was characterised by fascicles of dysplastic spindle cells, neuroid arrangement in loose fibrillary matrix, and peri- and intraneural permeation of the nerve trunks. Despite minimal atypism the neoplasm metastasised and had a fatal outcome. The spindle cell component of the neurotropic melanoma lacked melanogenesis; Fontana stains were negative. As previously demonstrated, the histogenesis of the neurotropic melanoma is possibly a Schwann cell differentiation of the dysplastic atypical melanocytes, as shown by the positive reactions to Bodian's stain.

Bone Neoplasms↗

Elemental diet as prophylaxis against radiation injury. Histological and ultrastructural studies.

We investigated whether elemental diet feeding would protect the intestine from radiation injury. Five dogs were fed an elemental diet for three days before receiving pelvic irradiation (500 rad/day for four days) and were maintained on the diet during the days of irradiation. These dogs were compared with five dogs that were fed normal kennel ration, but were treated similarly otherwise. One day and five days following completion of the radiation treatment, the dogs were anesthetized and a biopsy specimen of terminal ileum was taken for histologic and electron microscopic studies. In the dogs fed the elemental diet, there was no significant damage to the intestine seen on histological examination, and electron microscopy disclosed elongated microvilli and no organelle damage. However, both histological and electron microscopic examination of the intestine from dogs maintained on normal kennel ration showed that severe damage had occurred from the irradiation procedure. It seems, therefore, that the feeding of an elemental diet to dogs as a prophylaxis can afford protection to the intestine from the acute phase of radiation injury.

Animals↗

Development of experimental cancer in the head of the pancreas by surgical induction of tissue injury.

The majority of carcinomas of the pancreas in humans are of ductal origin and are located in the head of the gland. These clinical characteristics however, are not affected in traditional animal models of the disease. Partial pancreatic duct obstruction with ductal epithelial hyperplasia was produced in the Syrian golden hamster by wrapping the head of the pancreas with cellophane tape. Wrapped and unwrapped animals were then exposed to an exogenous carcinogen (N-nitrosobis[2-oxopropyl]amine). Assay of serum ribonuclease activity was used as a marker of disease. Invasive lesions developed in both groups of animals. Fifty percent of the tumors in the Group II (cellophane wrap and N-nitrosobis [2-oxopropyl] amine) hamsters were located in the head of the gland and were of ductal origin. All tumors in animals receiving N-nitrosobis [2-oxopropyl]amine alone (Group I) occurred peripherally and were derived from ductular or acinar tissue. Elevation of serum ribonuclease activity was noted early in the course of carcinogenesis, thereafter returning to normal, which may explain the clinical controversy regarding this marker. This new model should enhance our knowledge of the interrelationships between etiologic factors, precursor lesions, and pancreatic cancer.

Animals↗

Cholecystectomy stimulates hypertrophy and hyperplasia in the hamster pancreas.

Cholecystectomy may be a risk factor for carcinoma of the pancreas. In this study the morphometric and autoradiographic changes in the hamster pancreas following cholecystectomy (chole) were compared with changes observed in sham-operated controls. After operation significant increases were observed in percent acinar cell labeling with [3H]thymidine from 0.29 +/- 0.07 (controls) to 0.57 +/- 0.06 (chole) at 2 weeks and from 0.05 +/- 0.00 (controls) to 0.75 +/- 0.18 (chole) at 4 weeks. The number of labeled duct epithelial cells/mm duct length increased from 0.00 +/- 0.00 (controls) to 4.64 +/- 1.89 (chole) at 2 weeks and from 1.19 +/- 0.97 (controls) to 3.00 +/- 0.75 (chole) at 4 weeks. Duct epithelial cell height (micrometers) increased from 13.90 +/- 1.06 (controls) to 26.98 +/- 1.32 (chole) at 2 weeks and from 13.20 +/- 1.06 (controls) to 23.90 +/- 0.86 (chole) at 4 weeks. It was concluded that cholecystectomy results in hyperplasia and hypertrophy of pancreatic cell populations in the hamster. These data extend previous observations that cholecystectomy has a significant trophic effect on the pancreas.

Animals↗

Rational management of malignant colon polyps based on long-term follow-up.

We reviewed the long-term results of management of 38 patients with carcinoma in colorectal polyps. Of these, 16 patients demonstrated malignant invasion of the lamina propria but not the muscularis mucosa (group I), and 22 patients showed malignant invasion of the muscularis mucosa (group II). Primary therapy for group I patients consisted of polypectomy in 12, local excision in one, and colonic resection in three. One patient had a subsequent abdominal-perineal resection and was found to have no residual disease and no lymph node involvement. Follow-up of the group I patients showed that 11 were alive and well (mean 5.8 years) and five died of unrelated causes (mean 5.2 years). Of group II patients, 12 underwent polypectomy, six local excision, and four colectomy. Of these 22 patients, 11 underwent further operation, including nine major bowel resections and two local re-excisions. None of these 11 patients had either residual tumor or lymph node metastases. One patient died of complications after abdominal-perineal resection. Follow-up showed that 18/22 group II patients were alive and well 5 to 15 years later (mean 7.5 years); four died of unrelated causes (mean 3.2 years). We then reviewed another group of 220 patients who had undergone resection for invasive colon cancer to relate the presence or absence of lymph node metastases to the depth of malignant invasion in the bowel wall. We found that 44% of this entire group had lymph node involvement. Of 36 patients with tumor confined to the bowel wall, nodal metastases occurred in only 22%. Of eight patients with malignancy superficial to the muscularis propria, only one had nodal involvement. We conclude that colon cancer tends to progress in an orderly fashion and the risk of nodal metastases increases with the depth of invasion. Carcinoma in a polyp represents a very early stage of colon cancer. We therefore recommend polypectomy as primary treatment for pedunculated polyps containing carcinoma either superficial to or invading muscularis mucosa. If histologic review demonstrates incomplete excision, lymphatic invasion, or poor differentiation, patients with lesions invading the muscularis mucosa should undergo formal colonic resection.

Adenocarcinoma↗