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Biomedical subjects

C T Liu

Publications and source records attributed to C T Liu.

At least 55 records · Page 3Linked to original sources

From san gu liu po to 'caring scholar': the Chinese nurse in perspective.

This study presents a re-evaluation of the origins of Chinese nursing from the earliest traditional carers to the mature, professionalized institution of the republican period. The influence of traditional cultural values on the nature of the modern profession is discussed and its emergence considered in historical context with particular attention to the role of missionaries, philanthropic institutions and other aspects of foreign intervention, both European and Japanese. The Chinese anti-imperialist response, as stimulated by the 'May 4th Movement' and later the Sino-Japanese war, is shown to be an important ingredient in the transition from foreign to national control of the profession and in its achieving respect. Some doubt is cast on the assumption that Chinese nursing has followed a process of rapid convergence to the Western model.

China↗

Technique for repeated collection of cerebrospinal fluid from cisterna magna of anesthetized strain 13 guinea pigs.

To study biochemical changes in cerebrospinal fluid (CSF), we developed a reliable technique for repeated collection of CSF in anesthetized strain 13 guinea pigs. The animal's head was mounted in a stereotaxic instrument with ventral tilt at 30 degrees, and cisternal puncture was made with an L-shaped, 23-gauge needle through the shaved skin. Clear CSF was collected in a 1-ml syringe surrounded by crushed ice. Each collection procedure lasted for 3 min, and three consecutive collections produced about 0.2 ml of CSF. Sampling was repeated at 3-hr intervals. With intravenous saline infusion (10 ml/kg.hr), a total volume of 0.6-1.0 ml of CSF was collected over 6 to 12 hr. Animals maintained a mean blood pressure, heart rate, and minute volume, with few changes during CSF sampling for the entire collection.

Animals↗

Pulmonary responses of conscious strain 13 guinea pigs to Pichinde viral infection.

A laboratory animal model for studying pulmonary responses to arenaviral infection was established with advanced technologies. Tidal volume (TV), respiratory rate (RR), minute volume (MV), expiratory time (TE), inspiratory time (TI), peak expiratory flow (PEF), and specific pulmonary airway resistance (RES) were measured with a double plethysmograph and a computer data-acquisition system in six conscious, strain 13 guinea pigs. Using the same animal, experiments were conducted before and after subcutaneous inoculation with 10(4) plaque-forming units of Pichinde virus. Pulmonary functions were determined for 1 minute every 10 minutes for 2 hours before and at postinoculation days (PID) 3, 6, 8, and daily thereafter until shortly before death. The mean time to death was 18 +/- 0.7 days. Tidal volume, RR, MV, PEF, RES, and rectal temperature increased slightly on PID 3 and reached peak values at the midpoint of disease. At 95% of the mean time to death (16.5 +/- 0.5 days), RR, MV, and rectal temperatures suddenly decreased to lower than baseline values; while TV, RES, and PEF values remained high. When TE decreased with the increase in RR, TI did not change. When RR decreased at the terminal stage, both TE and TI increased. Hyperventilation, increased specific pulmonary airway resistance, terminal hypoventilation, and respiratory arrest were noted in strain 13 guinea pigs infected with Pichinde virus.

Airway Resistance↗

[A preliminary study on the role of interleukin-1 in chronic lung disease].

Pulmonary alveolar macrophages (PAM) obtained by bronchoalveolar lavage in 13 normal individuals, 17 lung cancer patients and 10 patients with chronic obstructive pulmonary disease (COPD) were incubated in vitro for 24 hours. Every specimen was divided into two portions and lipopolysaccharides were used to stimulate PAMs to produce interleukin-1 (1L-1) in one. The levels of 1L-1 in normal subjects were 5547.65 +/- 2420.42 cpm/10(6) cells (stimulated) and 718.46 +/- 472.25 (unstimulated), which were higher than the 2733.20 +/- 1611.17 (stimulated, P less than 0.01) and 327.57 +/- 226.86 (unstimulated, P less than 0.05) in lung cancer patients, but lower than that of 8716.26 +/- 2977.66 (stimulated, P less than 0.05) in COPD patients. The enhanced 1L-1 activity in COPD patients might contributed to the active inflammatory process and tissue destruction of COPD. Our findings that 1L-1 activity in patients with bronchogenic carcinoma was decreased may reflect the local immune deficiency in malignant disease. The release of 1L-1 by PAMs stimulated by smoking was suggested to be associated with the development of COPD, but its role in immune response has to be determined.

Aged↗

Changes in body weight and body surface area in strain 13 guinea pigs infected with Pichinde virus.

In studying pathogenetic mechanisms of Pichinde virus-induced disease in strain 13 guinea pigs, a large decrease of body weight (approximately 28%) observed within 14 days postinoculation raises a question concerning the validity of standardizing body or organ functions in terms of body weight. This study was to examine changes in body weight and body surface area of Pichinde virus-infected strain 13 guinea pigs after various days postinoculation. Control guinea pigs were also subjected to the same experimental procedures and experimental days. While body weights and body surface areas increased progressively in controls, I observed only slight decreases in body surface areas (4-6%) in the infected guinea pigs, despite large decreases of body weights throughout the 14-day experimental period. In conclusion, Pichinde virus-infected strain 13 guinea pigs demonstrated a small reduction of body surface area within 14 days postinoculation, suggesting that body surface area, rather than body weight, should be used for standardizing body or organ functions for comparison with their own baseline values.

Animals↗

Effect of ethanol on natural killer cell activity in vitro.

The effect of ethanol on kinetic stages of natural killer (NK) cell activity was studied in vitro. Peripheral blood mononuclear cells (MNC) were either co-cultured or pre-incubated with various ethanol concentrations and assayed for NK cell activity with a "4-hour chromium release assay" and a "single cell cytotoxicity assay in agarose" simultaneously. Direct addition of ethanol to the assay system resulted in a dose-dependent inhibition of NK cell activity. The percentage of lysed conjugated target cells was suppressed from a control value of 21.2% to 17.0%, 15.1%, 11.8% and 10.0% with an ethanol concentration of 0.125%, 0.25%, 0.5% and 1.0%, respectively. NK cell recycling was also inhibited. A 24-hour pre-incubation with ethanol, however, resulted in NK cell activity enhancement. The enhancement was around 20% with a 0.25% ethanol concentration and around 45% with a 0.5% and a 1.0% ethanol concentrations. The enhancing effect was noted mainly at the cytolysis stage after binding of effector cell with target cells.

Cells, Cultured↗

Body surface areas and K values in strain 13 guinea pigs with different body weights and ages.

Body surface areas (BSA) were determined for strain 13 guinea pigs with body weights ranging from 191 to 1011 g. For this determination, the entire skin of each animal was removed immediately after death and flattened on a wax film with a homogeneous paper. The skin outlines on the paper were cut and weighed for determining BSA. The K value was calculated for each guinea pig as the ratio of BSA (cm2)/body weight (g)2/3. Significantly different K values of 11.31 +/- 0.11, 9.66 +/- 0.09, 9.22 +/- 0.05, and 9.17 +/- 0.05 were determined for average body weights of 218 +/- 24, 527 +/- 33, 706 +/- 60, and 943 +/- 30 g, respectively. By plotting these K values on semilog paper and determining the best fit curve of the slope, it was possible to extrapolate exponentially the K values for different body weights. The relationship between age and body weight was also established for guinea pigs, and a series of K values were determined from birth to 35 weeks of life. We conclude that a different K value should be used for calculating BSA for various ages and body weights of strain 13 guinea pigs.

Aging↗

Transforming genes in duck hepatic carcinoma--mht(raf) and Ha-ras.

The transfection of NIH 3T3 cells was performed with DNAs from 2 duck primary hepatic carcinomas (DHC 40K, 9K) and 1 tumor-adjacent liver tissue (TAL, 9N). Transfectants were found from 40K, 9K and 9N DNAs. The secondary transfectants were obtained after transfection of RAT-1 cells with DNAs from primary transfectants. After hybridization with Ha-ras, Ki-ras, N-ras and mht oncogenes, it was found that duck mht (5.2 and 3.2 kb EcoRI fragments) and duck Ha-ras (3.4 kb EcoRI fragments) were present in all these transformants. This is the first report on transforming genes in duck primary hepatic cancer as well as tumor-adjacent liver tissue.

Animals↗

Energy balance and growth rate of outbred and inbred male guinea pigs.

Water intake, food consumption, growth rate, and rectal temperature were measured daily for 14 days and oxygen uptake was determined weekly for 3 weeks in healthy outbred (Hartley stock) and inbred (strains 2 and 13) male guinea pigs. Body weights ranged from 300 to 465 g, and ages were approximately 6 to 10 weeks. Strain-13 guinea pigs had the lowest daily body weight gain (3.27 +/- 0.33 g), when compared with strain-2 (4.04 +/- 1.21 g) and Hartley guinea pigs (5.72 +/- 1.08 g). Outbred guinea pigs also had highest values of water intake and water/food intake ratio(s), and had significantly (P less than 0.05 and 0.01) lower oxygen uptake values than did inbred guinea pigs. The ratio of daily average body weight gain to the corresponding daily retained calories, with or without corrections of body surface area (0.05 m2), was higher in Hartley stock than in the strain-13 guinea pigs. Rectal temperatures and food consumption were similar in all guinea pigs. Data indicated that the outbred Hartley guinea pig had a faster growth rate and appeared stronger physiologically, compared with inbred strains.

Animals↗

Observation of the in situ contracting heart of guinea pigs infected with Pichinde virus.

The in situ beating hearts from anesthetized control and Pichinde virus-infected strain 13 guinea pigs, between days 7 and 19 postinoculation, were directly observed and video recorded. Although some hearts from Pichinde virus-infected animals were visually depressed and had altered contraction patterns, such a pronounced cardiac dysfunction was not associated with any marked histopathological changes in the cardiac tissue. The manifestations of cardiac dysfunction were limited mainly to the right side of the heart and occurred only from days 11 to 19 postinoculation. We suggest that certain biochemical "lesions" in the heart after lethal Pichinde virus infection may be present, which may have been caused by the actions of endogenous pathogenic mediators and an overall metabolic deficiency of the infected body.

Animals↗

Evidence for the involvement of sulfidopeptide leukotrienes in the pathogenesis of Pichinde virus infection in strain 13 guinea pigs.

Strain 13 guinea pigs inoculated subcutaneously with Pichinde virus developed fever, lost body weight, decreased water and food consumption, and died at 14 +/- 0.6 days. After FPL-55712, a leukotriene D4 antagonist, was administered beginning on PID (post-inoculation day) 3 for 18 days, the magnitude of body weight loss decreased and food intake increased, despite a persistent fever. The treated guinea pigs also survived significantly longer than infected animals receiving placebo injection (21 vs 14 days). Using guinea pig ileum bioassay and radioimmunoassay, we detected significant levels of plasma leukotrienes in Pichinde virus-infected guinea pigs on PID 11 and possibly PID 14. These findings strongly suggest that leukotrienes play a role in the pathogenesis of arenavirus infection and may account in part for the observed cardiac depression, pulmonary edema, and eventual death.

Animals↗

Inhibition of overall protein and RNA synthesis as a mechanism for the tunicamycin induced decrease in cytochrome P-450 in rat hepatocytes.

In rat hepatocytes maintained in culture, cytochrome P-450 and NADPH cytochrome c reductase activities were decreased by tunicamycin in a dose and time dependent fashion. The effect of tunicamycin was mainly due to inhibition of protein synthesis. Tunicamycin decreased L-[35S] methionine incorporation into many proteins, including a 52 kDa cytochrome P-450 isozyme. Tunicamycin also reduced RNA synthesis. These results indicate that tunicamycin decreased cytochrome P-450 levels in hepatocytes by inhibiting protein and RNA synthesis.

Animals↗

Techniques for isolation and performance of the perfused guinea pig working heart.

This study demonstrated new approaches which enabled evaluating the work performance in both ventricles of an isolated guinea pig heart. By changing the right atrial filling pressure (RAFP, preload) from 6 to 20 mm of Hg at a constant aortic pressure (Pa, 20 mm of Hg), cardiac output, stroke volume, aortic flow, coronary flow, cardiac work, O2 consumption, CO2 output, as well as end-diastolic ventricular, and pulmonary arterial pressures increased. Cardiac contractility and both ventricular systolic pressures reached peak values between 12 and 14 mm of Hg of RAFP and then gradually decreased. With graded increases of Pa (afterload) from 10 to 45 mm of Hg at a fixed RAFP (8 mm of Hg), coronary flow, cardiac contractility, cardiac work, cardiac O2 consumption, glucose utilization rate, and pulmonary arterial and both ventricular systolic pressures increased. Although aortic flow decreased with an increase in Pa, cardiac output, stroke volume, and coronary resistance did not show significant changes. Furthermore, cardiac mechanical efficiency decreased with an increase of pre- or afterload of the perfused isolated heart. These findings indicate that the total working heart model is suitable for studying cardiac functions.

Animals↗

Inhibition of protein synthesis: a basis for tunicamycin-induced decrease in rat liver cytochrome P-450.

Tunicamycin caused a dose and time dependent decrease in cytochrome P-450 in rat liver. A dose of 50 micrograms/kg caused a decrease of about 50% in 72 hours. A similar decrease in the activities of rat liver microsomal aniline hydroxylase, aminopyrine N-demethylase and ethoxycoumarin O-deethylase were also seen after the tunicamycin treatment. Tunicamycin also suppressed food and water intake but the decrease in cytochrome P-450 was not related to these effects. NADPH cytochrome c reductase was not markedly decreased by tunicamycin. A decrease in cytochrome P-450 was also observed in cultured rat hepatocytes treated with tunicamycin. It decreased incorporation of [35S]-methionine into total proteins as well as into various cytochrome P-450 isozymes of rat hepatocytes. This indicates that a decrease in protein synthesis may be responsible for the tunicamycin-induced decrease in cytochrome P-450 and drug metabolism.

Animals↗