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Biomedical subjects

Y C Lin

Publications and source records attributed to Y C Lin.

At least 289 records · Page 16Linked to original sources

Seadragon VI: a 7-day saturation dive at 31 ATA. V. Cardiovascular responses to a 90 degree body tilt.

Cardiovascular deconditioning (CD) has been reported to occur in weightlessness, bed rest, and head-out water immersion. An expanded intrathoracic blood volume results, at least initially, in all these diverse conditions. Subjects in hyperbaric environments exhibit cephalad redistribution of blood volume, which also occurs in weightlessness, bed rest, and head-out water immersion. This physiologic similarity led us to suspect that CD may also occur as a consequence of hyperbaric exposure. We examined this possibility in 3 young male subjects during a 7-d dry saturation dive at 31 ATA. Changes in blood pressure, heart rate, and stroke volume were measured before and during 15 min of the 90 degree body tilt. These changes, expressed either singly or in combination, provided indications of CD during and immediately after hyperbaric exposure. One of the principal indicators of CD was the inability to exert adequate vasoconstriction. In addition, 1 subject fainted during hyperbaric exposure, whereas no such episode occurred before or after the exposure. These findings suggest that inappropriate orthostatic reflexes may be evoked by hyperbaria and reduced physical activity over the period of confinement. It should be noted, however, that CD was already evident within 24 h of hyperbaric exposure, suggesting that the initial phase of CD was unrelated to physical confinement. We postulate that CD occurs during hyperbaric exposure as an expression of cardiovascular and neurohumoral adaptation to an expanded central blood volume with a reduced total blood volume.

Adult↗

Taenia taeniaeformis: inhibition of mitogen induced proliferation and interleukin-2 production in rat splenocytes by larval in vitro product.

Splenocytes from rats infected with Taenia taeniaeformis showed an early decreased proliferative response to the mitogen concanavalin A with larval growth. When larvae culture supernatant (in vitro product) was added to normal rat splenocytes, there was a decrease in the proliferative response to concanavalin A and phytohemagglutinin. The ability of infected rat splenocytes to produce interleukin-2 was decreased with larval growth. Addition of in vitro product to culture medium significantly depressed interleukin-2 production by normal as well as infected rat spleen cells. Culturing normal rat splenocytes with in vitro product for 3 days induced a suppressor cell population. When these cultured cells were admixed with fresh normal rat splenocytes plus concanavalin A, the proliferative response of the fresh cells was significantly reduced. The present results suggest that in vitro product secreted by larvae in hepatic cysts causes subversion of the cellular immune response in the host. Induction of a suppressor cell population could suppress interleukin-2 production which may lead to the inhibition of differentiation and proliferation of specific cytotoxic T lymphocytes.

Animals↗

Taenia taeniaeformis: inhibition of metacestode development in the rat by gossypol.

The effect of gossypol, a polyphenolic compound, on developing Taenia taeniaeformis larvae in the rat liver was examined. Five groups of rats were used. In group 1, subcutaneous injection of gossypol at 10 mg/kg was started 5 days prior to administration of tapeworm eggs. In group 2, gossypol injections were started 5 days after administration of eggs. Groups 3 and 4 were infected and noninfected rats, respectively, which received the vehicle (10% ethyl alcohol in 0.85% NaCl) only. Group 5 rats were noninfected but received gossypol. From each group, 5 rats were killed on days 7, 12, and 22 of infection, respectively. The number and size of larvae and the size of the livers were much less in rats gossypol injected 5 days before infection than those in the vehicle-treated group. Administration of gossypol 5 days after infection resulted in less inhibition. The size and the thickness of the fibrous capsule around larvae of the gossypol-treated rats were much smaller than those of the control-infected group. The actively developing larvae excrete or secrete a sulfated glycosaminoglycan which is specifically stained with alcian blue. There was much more alcian blue-positive substance around the larvae and the capsule of the control-infected liver compared to the gossypol-treated infected animal. The percentage body weight of the spleen was significantly greater in the gossypol-treated rats in both infected and noninfected groups. These results suggest that gossypol may directly inhibit tapeworm larval development or that elimination of the tapeworm may be resulted from gossypol-induced stimulation of host cell-mediated immunity.

Animals↗

Taenia taeniaeformis: immunoperoxidase localization of metacestode culture product(s) in hyperplastic gastric mucosa.

Rats infected with the hepatic metacestode Taenia taeniaeformis develop an extraordinary gastric hyperplasia. Indirect immunoperoxidase staining localized larval in vitro excretory secretory product specifically in the supranuclear cytoplasm of the epithelial cells lining the pits and glands in the hyperplastic gastric mucosa. The accumulation of this substance in the stomach epithelial cells may be relevant to the gastric hyperplasia induced by tapeworm infection.

Animals↗

Post-treatments with sodium arsenite during G2 enhance the frequency of chromosomal aberrations induced by S-dependent clastogens.

Treatment with sodium arsenite during the G2 phase potentiated the chromatid breaks and chromatid exchanges induced by ultraviolet light or 4-nitroquinoline 1-oxide but not those induced by methyl methanesulfonate, ethyl methanesulfonate, mitomycin C or cisplatin in Chinese hamster ovary cells. A comparison was made between the effects of treatment during G2 with sodium arsenite, cytosine-beta-D-arabinofuranoside, aphidicolin, hydroxyurea, caffeine, 3-aminobenzamide and novobiocin on the frequency of chromosomal aberrations induced by the above-mentioned S-dependent clastogens. It was found that the effects varied considerably, both quantitatively and qualitatively. However, potentiation was more often observed in the chromosomal aberrations induced by ultraviolet light and 4-nitroquinoline 1-oxide than by other S-dependent clastogens, and the frequency of chromatid exchanges was potentiated only in cells pretreated with ultraviolet light or 4-nitroquinoline 1-oxide. Furthermore, for all of the S-dependent clastogens studied, treatment with cytosine-beta-D-arabinofuranoside during the G2 phase potentiated the frequency of chromatid breaks but not the frequency of chromatid exchanges.

Animals↗

Custom-made vaginal balloons for strengthening circumvaginal musculature.

A technique for making individualized silicone rubber intravaginal balloons is described. The method entails investing alginate vaginal impressions in silicone rubber and casting a resin model which is then dipped repeatedly in a Silastic Dispersion (Dow Corning, Q7-2213). The range of forces developed by circumvaginal muscles during maximum contractions was determined to be 0.5-4 lbs. Pressure-volume relationships of the balloons showed that the pressure of filling fluid was an accurate replica of the mean pressure in the vagina.

Female↗

Hypothermia impairs but hyperthermia does not promote inert gas elimination in the rat.

The volume of nitrogen eliminated (VN2) and washout rate constant (k) during a 2-h period of O2 breathing in the rat was altered in response to changes in body temperature. VN2 and cardiac output (Q) were determined simultaneously on 3 groups of unanesthetized but restrained male rats at 3 different body temperatures: normothermic (36 degrees C), hyperthermic (39 degrees C), and hypothermic (33 degrees C). Under normothermic conditions, the rats eliminated 12.8 ml N2/kg in 2 h of O2 breathing while Q, determined by a thermodilution technique, was 430 ml X min-1 X kg-1. A significant reduction in VN2 (33%) and k (44%) was seen during hypothermic exposures in which rectal temperature dropped 3 degrees C and Q decreased to 395 ml X min-1 X kg-1. During hyperthermic exposures, VN2, 11.7 ml N2/kg, and k decreased while Q increased to 468 ml X min-1 X kg-1, however, these changes were not significant when compared to the normothermic conditions. The overall relationship between VN2 and Q is described by: VN2 = 4.44 + 0.019 Q (r = 0.536, P less than 0.01). Under conditions of altered body temperature, Q accounts for only 29% of the VN2 response. Characteristic changes in regional blood flow, such as a decreased adipose tissue blood flow, may account for the observed reduction in VN2 and k during hypo- and hyperthermic conditions. The results of this study indicate that hypothermia prolongs the duration required for desaturation of nitrogen.

Animals↗

Cardiac output by impedance cardiography during head-out water immersion.

This study was undertaken to ascertain the suitability of impedance cardiography for qualifying cardiac output during water immersion where the electrodes were wet. The cardiac output was compared during wet and dry immersion with the head above water by breath holding briefly at 3 lung volumes. For dry immersion, the subjects were protected from contacting water during immersion by enveloping the whole body in a thin plastic bag. For wet immersion, the subject went into the water wearing only trunks. Eleven healthy males served as subjects. Both basal thoracic impedance and the minimum rate of impedance change decreased during wet immersion. These changes were specific, which insignificantly influenced the computation of stroke volume as compared to dry immersion. Our results showed no statistical differences between wet and dry immersions, and between measurements made at total lung capacity functional residual capacity, or residual volume. It is concluded that impedance cardiography is applicable directly in wet conditions without having to protect the subject from getting wet.

Adult↗

Effects of age and luteinizing hormone antiserum on human chorionic gonadotropin-stimulated testosterone secretion in young male rats.

The steroidogenic capacity of young male rats of different ages was studied. Two days prior to sacrifice at 5, 10, 15, 20, 25 and 30 days of age, the rats in treatment groups were given intramuscularly either human chorionic gonadotropin (HCG) at 20 I.U. twice daily/rat or luteinizing hormone (LH) antiserum (AS) at 0.25 ml twice daily/rat. Either saline or normal sheep serum (NSS) was given to control rats. The serum and testicular testosterone concentrations in the control rats averaged 0.85 +/- 0.03 ng/ml and 1.35 +/- 0.06 ng/mg testicular protein, respectively. At day-15 the serum and testicular testosterone concentrations in the HCG-treated rats had significantly increased to 9.30 +/- 0.85 ng/ml and 11.92 ng/mg of testicular protein, respectively. At the same age, the HCG-induced higher levels of serum and testicular testosterone concentrations were significantly reduced to 2.80 +/- 0.70 ng/ml and 6.02 +/- 1.00 ng/mg protein by concomitant administration of LH/AS and HCG. Our results suggest that the testosterone production in response to HCG stimulation is age-related. It was also determined that neutralization of circulating gonadotropin in LH/AS-treated rats decreased the sensitivity of Leydig cells to gonadotropin stimulation. This in vivo model should provide an excellent opportunity for the investigation of the testicular function in developing young males.

Age Factors↗

Gossypol in female fertility control: ovum implantation and early pregnancy inhibited in rats.

Intramuscular administration of gossypol to normally cycling female rats induced an irregularity of the cyclic pattern for as long as the treatment was continued. Furthermore, administration of gossypol from days 0 (day of sperm-positive vaginal smear) to 8 of pregnancy prevented the normal maintenance of pregnancy. Serum values of progesterone and estradiol 17 beta in gossypol-treated normally cycling and pregnant rats were significantly lower than the control levels. The supplement of a combination of exogenous progesterone and estradiol 17 beta eliminated the inhibitory effects of gossypol on ovum implantation and the maintenance of pregnancy. Our results indicate that gossypol may have some usefulness in female fertility control.

Animals↗

Histopathologic changes of uterus following gossypol treatment during early pregnancy in rats.

Intramuscular injections of gossypol acetic acid (25 mg in 10% EtOH/kg/day beginning on day 2 of diestrus) disrupted early pregnancy in rats as determined by light and electron microscopy. As in pregnant controls, in the uteri of treated rats increased glandular secretion, stromal hyperemia, and decidual tissue formation were noted at days 3-5 of pregnancy. At day 6, extreme hyperemia and stromal hemorrhage had occurred around well-developed decidual tissue with foci of denuded mucosal surface. There was extravasation of blood into the uterine lumen, which was absent in controls. At days 5 and 6 of pregnancy, electron microscopy revealed shorter and fewer microvilli on the uterine glandular cells in the treated versus the control uterus. Luminal epithelial cells had not undergone the normal changes of pregnancy. These results imply that gossypol administered under our conditions neither prevented nor delayed implantation and formation of decidual tissue in the rat uterine endometrium but continuing development of the endometrium was disrupted at day 6 of pregnancy. This disruption of pregnancy may have resulted from a luteolytic action by gossypol that would not permit full structural differentiation in the rat uterus after implantation.

Animals↗

Taenia taeniaeformis: inhibition of rat testosterone production by excretory-secretory product of the cultured metacestode.

In 3- to 5-month-old male Sprague-Dawley rats infected with the hepatic metacestode, Taenia taeniaeformis, the serum testosterone level was significantly lower than in comparable uninfected controls. By transmission electron microscopy, testicular Leydig cells of infected rats had less smooth endoplasmic reticulum than control Leydig cells. Cultured metacestodes isolated from the hepatic cysts secreted or excreted substances into the incubation medium. The effect of the excretory-secretory product on testosterone concentration in the sera and testes of 15-day-old rats was examined. Subcutaneous injection of 50-200 micrograms of excretory-secretory product/0.1 ml saline/rat for 2 days significantly reduced human chorionic gonadotropin-stimulated serum and testicular testosterone concentrations. Furthermore, the effect of the excretory-secretory product on isolated rat Leydig cell testosterone production was examined. Rat Leydig cells produced testosterone in vitro and, in the presence of 50 IU human chorionic gonadotropin/ml incubation medium, they responded with approximately 100% increase in testosterone production. Addition of 2-10 micrograms excretory-secretory product protein/ml of culture medium significantly reduced the testosterone production by rat Leydig cells in vitro. These results indicate that excretory-secretory product of cultured T. taeniaeformis metacestodes has a direct inhibitory effect on Leydig cell testosterone production under stimulation with human chorionic gonadotropin.

Animals↗

Diurnal, premating, and postmating testosterone levels in roosters genetically selected for mating frequency.

Circulating testosterone (T) levels were measured in roosters from lines genetically selected for high (HM) and low (LM) mating frequency and the randombred control (AC) base population. Lights were provided from 0600 through 2000 hr. A dirunal profile was determined by sampling at 0600, 1200, 1800, and 2400 hr. Plasma T levels prior to mating, immediately after mating, and 1 and 3 hr after mating were measured. By 1800 hr, AC males had higher T levels than both HM and LM males, which had levels that were similar to each other. Testosterone was at a minimum at 0600 hr and peaked at 2400 hr. Lines differed significantly both before and after mating with AC males highest, HM males intermediate, and LM males lowest. Control males had higher than baseline values prior to and after mating. Testosterone levels of AC males were correlated with their mating frequencies.

Analysis of Variance↗

In vivo and in vitro inhibition of human chorionic gonadotropin-induced testosterone production in rat testis by bursa of fabricius extract.

A bursa of Fabricius homogenate extract (BHE) was used to investigate the endocrine regulation function of this avian organ. In vivo and in vitro results indicated that BHE inhibited human chorionic gonadotropin (HCG)-induced testosterone production by rat testes. Leydig cells from collagenase-dispersed rat testes, when treated with BHE, showed a dose-response related depression of testosterone production under HCG stimulation. Young male rats, injected simultaneously with BHE and HCG, failed to show the marked testosterone production peak observed in rats injected with HCG only. However, in vivo treatments with BHE, in the absence of HCG stimulation, did not inhibit basal testosterone production. These results indicate that the bursa of Fabricius produces an endocrine regulation factor that inhibits HCG-induced testosterone production both in vivo and in vitro. Further investigation is necessary to isolate the active factor and determine its mechanism of action.

Animals↗

Taenia taeniaeformis: increased cell growth and neutral mucus production in the gastric mucosa of the rat with a larval infection.

Gross hyperplasia of the gastric mucosa and excessive mucus production in the stomach occur in rats heavily parasitized with larvae of Taenia taeniaeformis. In this study, a positive correlation between the number of larvae recovered from hepatic cysts and the weight of the stomachs of infected rats was found. By light microscopy, the hyperplasia was restricted to the glandular mucosa. Parietal and chief cells were very rare, and densely PAS-positive mucous cells were the major cell types in the hyperplastic stomach while, in comparison, alcian blue-positive cells were much fewer in number. The isolated gastric mucosa in organ culture had an increased [3H]thymidine incorporation rate in rats infected with T. taeniaeformis. The hexosamine concentration per milligram protein in the hyperplastic stomach mucosa was twice that in the control rat stomach mucosa. By electron microscopy, the apical cytoplasm of the mucous cells was found to be filled with small dark granules. These results indicate that the gastric hyperplasia is caused by stimulation of growth and major differentiation of stem cells to neutral mucus-producing cells.

Animals↗

Influence of blood flow on cutaneous permeability to inert gas.

A thermally regulated Plexiglas chamber was designed for investigation of transcutaneous diffusion of N2 and helium (He) in the human hand. Influence of cutaneous blood flow in this process was studied simultaneously with gas diffusion measurements. Changes in cutaneous blood flow (Q, in ml X min-1 X 100 ml tissue-1) were effected by altering ambient temperature (T) from 20 to 40 degrees C (Q = 0.08 X 100.07T). We found that the rate of inert gas diffusion through human skin, expressed as conductance (G, in ml STPD X h-1 X m-2 X atm-1), increases exponentially as a function of blood flow, and was indistinguishable between He and N2 (G = 21.19 X 100.0124Q). The permeability, diffusion coefficient per unit diffusion distance (D/h, in cm/h), also rose exponentially as a function of blood flow. But permeability for He (D/h = 0.1748 X 100.0203Q) was greater than that for N2 (D/h = 0.1678 X 100.0114Q). As cutaneous blood flow rises, because of increased temperature, the apparent diffusion distance falls linearly for both N2 and He. The change is more prominent for He than for N2 diffusion. Estimated replacement time for the body stores of N2 by transcutaneous diffusion alone was shortened from 26.8 h at 31 degrees C to 15.1 h at 37 degrees C. It is suggested from this study that beneficial results may be derived during decompression procedure 1) by maintaining an appropriate transcutaneous pressure gradient of inert gases, and 2) by elevating ambient temperature.

Capillary Permeability↗