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Biomedical subjects

G D Cain

Publications and source records attributed to G D Cain.

At least 37 records · Page 2Linked to original sources

Natural history of benign esophageal stricture treated by dilatation.

Although bougienage is widely used to treat benign esophageal stricture, the rate of stricture recurrence and the long-term effectiveness of bougienage are unknown. We studied the natural history of esophageal stricture in 154 patients in whom bougienage was used as primary therapy. Dilatations were considered successful in terms of relief or major improvement of dysphagia in 84.5% of 103 patients followed 6 mo or longer (median, 26 mo). The risk of requiring esophageal dilatation after the initial episode was greatest in the first year of follow-up; thereafter, a smaller fraction of patients required dilatation each year. Forty-three percent of patients required no further dilatations, and a life-table analysis showed that 36% of patients would require no further dilatation during a projected 4-yr follow-up. The median frequency of subsequent dilatation was less than once a year. We were unable to identify any significant factors, such as initial severity of stricture, cause of stricture, presence of active esophagitis, or initial caliber of dilatation, that could predict the need for subsequent dilatation. Our results suggest that patients with benign strictures fall into two groups. In one group, the natural history was to improve or become asymptomatic after an initial series of dilatations, and only a small proportion eventually developed recurrent symptoms. The second group (46% of patients) required further dilatations to treat dysphagia during the first year of follow-up. Two-thirds of these patients needed regular dilatations in subsequent years. We conclude that bougienage is effective treatment for benign esophageal strictures, and should be utilized as primary therapy for most strictures.

Adult↗

Enzyme polymorphism in Ascaris suum (Nematoda).

The potential of multilocus electrophoretic studies for providing insight into the population biology of parasitic organisms was studied using the swine parasite Ascaris suum suum. Thirty-eight loci encoding enzymatic or nonenzymatic proteins have been resolved in extracts of adult worms by starch-gel electrophoresis. A preliminary study of variation in Ascaris from eastern Iowa revealed an average heterozygosity of 6.6%. Allele frequencies at six polymorphic loci were similar in males and females and genotypic frequencies were in accord with those expected in a single, randomly mating population; however, the significant linkage disequilibrium between Pep-2 and Es-3 suggested that there may be some genetic substructuring within Ascaris from Iowa. Genetic comparisons of Ascaris from Iowa with Ascaris from New Jersey and Maryland indicated slight differences between eastern and midwestern populations, as well as between the east coast localities. Larger samples from more locations are needed before any statistical significance can be attached to these differences; however, qualitative comparisons suggest that the differentiation is a biological reality. Knowledge of the population biology of this and other parasites may contribute to planning effective control programs.

Animals↗

Gastric radiotherapy as treatment of hereditary hemorrhagic telangiectasia.

A patient with hereditary hemorrhagic telangiectasia and von Willebrand's disease is described. He suffered recurrent episodes of gastrointestinal bleeding endoscopically localized to the cardia and body of the stomach. A cobalt 60 source was used to deliver 1600 rad to the patient's stomach. The effect of the radiation was remarkable in that he remained free of bleeding for more than 11 months. Radiotherapy should be considered for control of gastric bleeding in hereditary hemorrhagic telangiectasia.

Gastrointestinal Hemorrhage↗

Prospective evaluation of biopsy number in the diagnosis of esophageal and gastric carcinoma.

A prospective trial was performed in which biopsy and cytology specimens were obtained on 202 consecutive patients including 47 with esophageal or gastric carcinomas. The first biopsy specimen yielded a correct diagnosis in the majority of instances: 70% of gastric carcinomas and 93% of esophageal carcinomas. Three additional biopsy specimens increased the yield to greater than 95%, a total of seven biopsy specimens yielded greater than 98%. Seven biopsy and cytology specimens yielded the correct diagnosis in all patients. Seventeen percent of all lesions subsequently proven to be malignant were thought to be benign, endoscopically. This reinforces the belief that all lesions seen at endoscopy should have biopsies performed and at least seven specimens should be obtained.

Biopsy↗

Subcellular fractions and the refringent granules of the spermatozoa of Ascaris suum (Nematoda).

Six subcellular fractions were isolated by differential centrifugation of the homogenate of spermatozoa of Ascaris suum. The cellular constituents of pelleted fractions, as identified by electron microscopy, were membranes and membranous organelles (fraction A1), microsomal (A2), cytoplasmic (A3), large refringent granules (B1), small refringent granules (B2) and a detergent-soluble fraction (B3). Polypeptide analysis of SDS-PAGE showed that the 18,400-dalton band, one of the major spermatozoan proteins, is detectable in all of the fractions. However, the cytoplasmic (A1) and refringent-granule (B1) fractions contained the highest level. The isolated refringent granules consisted of 2-6% lipid while the nonlipid fraction formed an insoluble matrix with a fibrillar network morphology. This fibrillar matrix contained three polypeptides of small molecular weight (7,000-14,000) in addition to the 18,400-dalton polypeptide. These small polypeptides (7,000--14,000 MW) are detectable only in fractions of the refringent granules and are therefore called the refringent-granule proteins (RGP). These RGP are sensitive to tryptic hydrolysis and have solubility properties similar to the protein, ascaridine.

Animals↗

Surface receptors: are they involved in transformation of spermatozoa of Ascaris?

Exposure of the spheroidal spermatozoa of Ascaris suum to an extract of the male accessory gland causes their transformation into ameboid cells. We have investigated the mechanism of this transformation, also termed activation, by labeling the proteins of accessory gland extracts with fluorescein isothiocyanate (FITC) or [125I], followed by qualitative localization of the sperm activating substances (SAS) and quantitative measurements of [125I]-SAS binding. Fluorescent patches of FITC-conjugated SAS were localized at the spermatozoan surface and were concentrated primarily at the posterior region. Few fluorescent patches were detectable in the region of the newly formed pseudopodia following transformation. Although spermatozoan transformation occurs within 2-5 min after exposure to SAS, the fluorescent patches became more distinct after a minimum of 8 min and reached maximum density at 15-30 min. Spermatozoa activated with [125I]-SAS became radioactively labeled in direct proportion to the amount of available [125I]-SAS until a saturation level was reached. SDS-polyacrylamide gel electrophoresis combined with autoradiography indicated that the cells bind two SAS components, of small (9,000 MW) and large (56,000 MW) sizes. These same two components were also detectable in a membrane fraction, obtained by differential centrifugation, of the spermatozoa after incubation with [125I]-SAS. binding of the two SAS components was not inhibited by preincubation of the spermatozoa with trypsin or Concanavalin A; however, the 56,000 MW component of SAS was not detectable in autoradiograms of spermatozoa incubated with periodic acid (1.6-10 mM) treated SAS. Such cells also failed to transform into ameboid spermatozoa. These results indicate that the two components of SAS that bind to the spermatozoan surface are possibly responsible for inducing the cell transformations associated with activation.

Animals↗

Karyotype evolution and sex chromosome differentiation in Schistosomes (Trematoda, Schistosomatidae).

The morphology of C-banded metaphase chromosomes has been studied in two hermaphroditic and ten gonochoristic digenetic trematodes (schistosomes). Comparison of numbers and morphology of chromosomes indicates that the karyotype of primitive trematodes probably was composed of 10 (or 11) pairs of telocentric or subtelocentric chromosomes, and reduction of chromosome numbers in advanced species resulted from centromeric fusion rather than elimination of chromosomes. Observation of heteromorphic chromosomes in a hermaphroditic trematode (Spirorchis) suggested a differentiation of "pre-sex" chromosomes in species ancestral to dioecious trematodes which possess distinctly differentiated sex chromosomes. Our results indicate that differentiation of Z and W chromosomes in the gonochoristic trematodes resulted from: (a) partial constitutive heterochromatinization of the W chromosome (Schistosoma mansoni and S. haematobium complexes, African schistosomes), (b) deletion of part of the W (S. japonicum and S. mekongi, Asian schistosomes), and (c) translocation of part of one sex chromosome onto another (Schistosomatium douthitti and Heterobilharzia americana, American schistosomes) with subsequent heterochromatinization of the W in H. americana.

Animals↗

Disruption and removal of the tegument from Schistosoma mansoni with triton X-100.

Tegumental membranes of Schistosoma mansoni were disrupted by 0.2% Triton X-100 in Tris-maleate buffered/Kreb-Ringer's solution. Subsequent differential centrifugation of the disruption solution at 2,500 g and 30,000 g produced two pellets which contained membrane components. Examination of the carcass by scanning electron microscopy revealed that most of the exposed tegument of both male and female worms was removed, while surface membrane protected by close apposition of another surface (i.e., in the gynecophoral canal) remained intact. The parenchymal tissue (e.g., subtegumental muscle and tegumental perikarya), excretory and gut epithelia, and the tegument's basement membrane also remained intact. The selectivity of the disruption suggests that membrane in both pellets originated almost exclusively from the tegument. Although larger morphological features (i.e., surface crypts) present in the intact tegument did not maintain their form in the 2,500 g pellet, the high specific activity of 3H-concanavalin A retained by this fraction, and the presence of numerous spines and large pieces of membrane, suggest that the 2,500 g pellet contained most of the worm's disrupted surface membrane. Transmission electron microscopy demonstrated the presence of dense spinelike material and vesicles of various sizes and densities, as well as some mitochondria in the 30,000 g pellet. Low specific activity of 3H-concanavalin A in the post-30,000 g supernatant suggests that relatively few externally oriented, saccharide-containing molecules were solubilized from tegumental membranes by Triton X-100.

Animals↗

In vitro activation and behavior of the ameboid sperm of Ascaris suum (Nematoda).

A system is described for the study of activation and motility of Ascaris spermatozoa in vitro. Activation was accomplished by addition of the sperm-activating substances (SAS), extracted from the male accessory gland, to cells incubated in phosphate-buffered saline (pH 7.4) at 37-39 degrees C under anaerobic conditions (95% N2, 5% CO2). Activation is characterized by a change from spherical to ameboid shape with coalescence of the refringent granules. The normal ameboid spermatozoa bear several stubby and needle-like filopodia at the lamellipodial margin. Within the lamellipodium are bundles of microfilament-like structures extending toward the pseudopodial membrane and concentrating within the needle-like filopodia. These filopodia exhibit a pendulous, sweeping motion with subsequent retraction and disappearence within the main lamellipodium. Membranes of the ameboid cells interact at the pseudopodial regions with partial fusion, as suggested by apparent membrane breakdown between interdigitating portions of the pseudopodia. Activation is complete in 5-15 min, is totally inhibited at 4 degrees C and/or by an atmospheric environment, but can be reinitiated by transfer to anaerobic conditions at 22-39 degrees C. Activation also requires favorable pH (6.8-8.7) and continual exposure to sufficiently high sodium concentrations (134-154 mM), i.e., lowering of sodium concentration to 10 mM causes irreversible inactivation. Sodium may be replaced by potassium or lithium but not by Tris or sucrose. Proteinases (10 microgram/ml) can act as activators even though SAS lack detectable proteolytic activity against azoalbumin, azocasein, TAME and BTEE and SAS activation was not inhibited by TLCK or soybean trypsin inhibitor.

Animals↗

Methoxyflurane hepatitis.

A veterinarian's assistant who sniffed methoxyflurane as a euphoriant developed fulminant hepatitis and died of hepatic failure. The abuse of fluorinated anesthetics has been reported and may be more frequent than is commonly believed. It is suggested that fluorinated anesthetics should be considered as a causative agent in a case of fulminant hepatitis, especially in patients who have easy access to such drugs.

Adult↗

A simple method of obtaining an enriched fraction of tegumental brush border from Hymenolepis diminuta.

A method for isolating an enriched preparation of tegumental brush border from the tapeworm, Hymenolepis diminuta, is described. Combining incubation of whole tapeworms in Krebs-Ringer/tris-maleate solution containing a hemolytic saponin, low shear-force agitation, and differential centrifugation, a pellet is obtained at 2,500 g which contains a significant concentration of surface brush border. The content of brush border in this fraction is identified by the presence of numerous microvilli, increased specific radioactivity after surface tagging with 3H-Concanavalin A, and relatively little mitochondrial contamination (succinic dehydrogenase). Based on morphological criteria, fractions sedimenting with greater force contain dense vesicles and mitochondria from the outer portion of the tegument.

Cestoda↗