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Biomedical subjects

Y Gotoh

Publications and source records attributed to Y Gotoh.

At least 289 records · Page 16Linked to original sources
PubMed1981

A simple plaque assay method for antibody-dependent cell-mediated cytotoxicity using Cunningham's chamber.

An improved and simpler plaque assay method for antibody-dependent cell-mediated cytotoxicity using Cunningham's chamber has been developed. Effector lymphocytes, target sheep red blood cells (SRBC) and anti-SRBC serum were incorporated together into a Cunningham's chamber and, immediately after making monolayers, incubated at 37 degrees C for 20 h. A hemolytic plaque of SRBC was formed around a lymphocyte in the presence of anti-SRBC serum, which was inhibited specifically by addition of aggregated IgG or Fc-fragment of human IgG in the culture. A hemolytic plaque formed around a monocyte-like cell was clearly differentiated from those around a lymphocyte (K-cell). The percentage of plaques in the purified lymphocytes from healthy individuals correlated significantly with ADCC activity measured by 51Cr-release. The method is a significant improvement on the earlier plaque assay methods with regard to: (1) making the monolayer, (2) observation and counting of plaques, and (3) shortening the time required for assay. Thus, the method should be valuable for clinical studies of cytotoxic activity in ADCC systems in healthy and diseased persons.

Animals↗
PubMed1981

[Pharmacological study on hydrocortisone 17-butyrate 21-propionate (author's transl)].

The topical and systemic anti-inflammatory activities of hydrocortisone 17-butyrate 21-propionate (HBP) were studied. The systemic anti-inflammatory activities of HBP and reference steroids were examined for their effects on dinitrochlorobenzene dermatitis, carrageenin edema, cotton pellet granuloma and adjuvant arthritis in rats and by the delayed allergic edema test in mice. The topical anti-inflammatory activities of these steroids were examined for their effects on croton oil dermatitis, croton oil ear edema, carrageenin edema and cotton pellet granuloma in rats. Furthermore, effects of these steroids on liver glycogen deposition in mice, thymolysis, and decrease of serum corticosterone level in rats were examined. Systemically administered HBP was less potent than betamethasone 17-valerate (BV), but was almost equal to hydrocortisone 17-butyrate (HB) in anti-inflammatory activity, and its effects on liver glycogen deposition, thymolysis, and the decrease of serum corticosterone level. However, the topical anti-inflammatory activity of HBP was more potent than that of BV and HB, although in the same experiment, thymolytic activity of HBP was less potent than that of BV, but was almost equal to HB. The inhibitory effect of HBP on hypotonic induced hemolysis was weaker than that of BV, but was stronger than that of HB in vitro. The affinity of HBP was higher than that of BV and HB to polymorphonuclear leucocytes used as the inflammatory cells in vitro. On the other hand no marked difference was observed in the affinity to erythrocytes used as the non-inflammatory cells in vitro. These results suggest that HBP is a useful drug which has superior topical anti-inflammatory activity, but has a weak systemic effect.

Animals↗
PubMed1981

[Effects of anti-inflammatory drugs on the arachidonic acid induced erythema in guinea pigs (author's transl)].

The inhibitory effects of anti-inflammatory drugs on th erythema induced by arachidonic acid in guinea pigs were studied. Values of ED50 (mg/kg, p.o.) were; diclofenac sodium (19.9), indomethacin (28.1), naproxen (52.4), phenylbutazone (67.1), ibuprofen (81.3), aspirin (92.6). These drugs, however, were ineffective on the erythema induced by prostaglandin E2. Basic nonsteroidal and steroidal anti-inflammatory drugs and anti-oxidants were negative in the inhibition of arachidonic acid-induced erythema. Cyproheptadine as an anti-histamine and -serotonin agent and morphine as a CNS acting agent were also negative. Erythema did not occur following treatment with linoleic acid, linolenic acid and gamma-linolenic acid. Bishomo-gamma-linolenic acid-induced erythema was inhibited by diclofenac sodium. The inhibition of acidic nonsteroidal anti-inflammatory drugs in this system seemed to be the result of a block of the enzymatic conversion of arachidonic acid to prostaglandins. The arachidonic acid-induced erythema in guinea pigs can serve as a new animal model for evaluating prostaglandins biosynthesis inhibitors such as anti-inflammatory drugs.

Animals↗
PubMed1980

Dietary regulation of hepatic 3-hydroxy-3-methylglutaryl-CoA reductase and cholesterol synthetic activities in fasted-refed rats.

Effects of dietary cholesterol, beta-sitosterol and cholestyramine on hepatic HMG-CoA reductase activity and sterogenesis were examined in male rats refed different types and amounts of fats for 3 days after fasting 2 days. Safflower oil (10%) decreased reductase and sterogenic activities more than saturated fat or low fat. Reductase activity and sterogenesis decreased as dietary cholesterol increased; this was not influenced by the type of dietary fat. Although cholesterol as low as 0.01% depressed these activities, more cholesterol was required to deposit cholesterol in the livcreased cholesterol excretion as neutral steroids but failed to enhance reductase and sterogenic activities. In contrast, cholestyramine increased these activities to approximately the same level irrespective of the type and amount of dietary fat. Hepatic cholesterol decreased only in rats refed saturated fat; neutral or acidic steroid excretion was greatest in this group. Hepatic cholesterol and enterohepatically circulating cholesterol may not be critical factors in regulating HMG-CoA reductase in fasted-refed rats. Rather, the quantity of bile acids fluxed to the liver appears to influence the reductase activity in this situation. However, analyses of fecal acidic steroids provided no evidence for a relationship between HMG-CoA reductase activity, bile acid metabolism and dietary fat.

Animals↗
PubMed1979

Synthesis of procollagen by odontogenic cells of rabbit tooth germ.

Studies were performed to determine whether cultured odontogenic cells from rabbit tooth germ (RP cell) could synthesize dentine-like collagen. When cells were cultured with [14C]proline, 33% of the total incorporated proteins present were collagenous. Cultured RP cells were labeled with [14C]proline in the presence of beta-aminopropionitrile. The resulting fractions, on analysis by CM-cellulose chromatography, contained three radioactive protein peaks, alpha 1(I), [alpha 1(III)]3, alpha 2. From the radioactive measurements, RP cells synthesized a significant amount of type III collagen, comparable to type I collagen. DEAE-cellulose chromatography was used to separate collagen molecules from collagen precursors. The results showed that 60% of total collagen precursor was type III precursor and the remainder was type I precursor. CM-cellulose chromatography of CNBr peptides of collagen from culture medium and cell extract revealed the presence of type I and type III collagen. Thus, the RP cell, which is a diploid cell, is unique in the predominance of type III collagen in culture, differing thereby from the character of collagen in vivo.

Animals↗
PubMed1979

Synthesis of procollagen by dental pulp cells from incisor in vitro.

Fibroblast-like cells were isolated from dental pulp of rabbit incisor, and were shown to synthesize and secrete procollagen. Analysis of the secreted procollagen and their CNBr peptides indicated that the prominent form was type I procollagen. Our results also suggested the presence of type III procollagen as a minor component synthesized by pulp cells in vitro.

Animals↗
PubMed1977

Malignant hyperthermia and althesin.

General anaesthesia with Althesin was administered on two occasions to a patient who was identified as susceptible to malignant hyperthermia, in whom there was identified familial subclinical myopathy and once in another patient suffering from arthrogryposis multiplex congenita with a history of fever associated with two previous anaesthetics. In the first patient halothane was administered by accident in association with the Althesin, but no hyperpyrexia occurred. In the second instance nitrous oxide-oxygen and halothane were associated purposely with Althesin. In none of these cases was there any rise in temperature, muscle rigor or elevation of the serum CPK level. This experience corroborates the experimental evidence of Hall, et al.10 and Harrison, who reported that Althesin prevented the onset of hyperthermia, and the clinical reports of Page and Judelman. Althesin can be assumed to be an effective anaesthetic for malignant hyperthermia susceptible patients.

Alfaxalone Alfadolone Mixture↗