
| JaLCDOI | 10.18926/AMO/32222 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Yoshida, Toshiko| Itoh, Yoshinori| Gomita, Yutaka| Oishi, Ryozo| |
| 抄録 | The release of indomethacin from fatty-base suppositories, which had been stored at a low (4 degrees C) and a high (25-30 degrees C) temperature for about one month, was examined in vitro and in vivo. In the in vivo experiments, the plasma indomethacin levels after administration of suppositories stored at different temperatures were measured in conscious and anesthetized rats. In the in vitro release test using a dialysis cell method, much lower amounts of indomethacin were released from the suppositories stored at a high temperature than from those stored at a low temperature. The melting point of suppositories stored at a high temperature was higher by approximately 2 degrees C than those stored at a low temperature. In conscious rats, the plasma indomethacin levels attained after the intrarectal administration of suppositories stored at a high temperature were slightly lower than those after the animals were given suppositories stored at a low temperature, but the difference was significant only 30 min after administration. In anesthetized rats, the plasma indomethacin levels were markedly lower than those in conscious rats, and the influence of the storage temperature on the plasma indomethacin levels was clearly observed. These results suggest that in conscious rats many factors such as a locomotor hyperactivity and enhancement of gastrointestinal motility caused by the rectal administration mask the real character of suppositories. The in vitro and in vivo results show that the release of indomethacin from fatty-base suppositories stored at a high temperature is less than the release from those stored at a low temperature. |
| キーワード | indomethacin suppository quality contyol bioavailability in vitro release test |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 37 |
| 終了ページ | 42 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 2063694 |
| Web of Science KeyUT | A1991FA75000005 |
| JaLCDOI | 10.18926/AMO/32221 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Suemaru, Shuso| Kageyama, Jingo| Ota, Zenske| Ohnoshi, Taisuke| Sakamoto, Kenji| Kamura, Junta| |
| 抄録 | A patient with a diffuse, small cleaved cell, non-Hodgkin's lymphoma associated with marked hypecalcemia was described. Antibody to the adult T-cell leukemia-lymphoma virus was absent. Although bone marrow was infiltrated by lymphoma cells, destructive or lytic bone lesions could not be detected. The serum level of immunoreactive parathyroid hormone C-terminal (PTH-C) was normal. The serum level of 1, 25-dihydroxyvitamin D was lower than normal. This case suggests that other humoral substances produced by lymphoma cells may be responsible for hypercalcemia.</P> |
| キーワード | hypercalcemia non-Hodgkin7s lymphoma bone resorption parathyroid hormone(PTH) 1 25-dihydroxyvitamin D |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 55 |
| 終了ページ | 59 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 2063696 |
| Web of Science KeyUT | A1991FA75000008 |
| JaLCDOI | 10.18926/AMO/32220 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Yoshida, Iwao| Takamizawa, Akihisa| Fujita, Hiyoyuki| Manabe, Sadao| Okabe, Akinobu| |
| 抄録 | We constructed a plasmid, pBH103-ME5, in which the region encoding the 10 preS2 amino acid residues and the S domain of the hepatitis B surface antigen (HBsAg) were regulated by the promoter of the yeast repressible acid phosphatase gene. Saccharomyces cerevisiae carrying pBH103-ME5 produced the HBs antigen (yHBsAg), when it was cultured in a medium containing a low concentration of phosphate. The antigen was purified to homogeneity. Its molecular weight was determined by Western blotting to be 24,000, and its amino acid composition agreed well with that deduced from the nucleotide sequence. The C-terminal amino acid sequence of yHBsAg was exactly the same as that predicted from the nucleotide sequence, while the N-terminal amino acid acetylserine, which was followed by 8 amino acid residues coded by the preS2 region. These results indicate that the recombinant yeast produced a single polypeptide consisting of the preS2 region and the subsequent S domain after being processed at the N-terminus |
| キーワード | hepatitis B surface antigen preS2 region plasmid yeast Saccharomyces cerevisiae |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 1 |
| 終了ページ | 10 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 2063691 |
| Web of Science KeyUT | A1991FA75000001 |
| JaLCDOI | 10.18926/AMO/32219 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Meguro, Tadamichi| Ogata, Masana| |
| 抄録 | Pulmonary function tests were performed on 252 healthy young subjects free from respiratory and allergic symptoms, and 80 young subjects with past history of nasal allergy (PNA) and 10 subjects with past history of bronchial asthma (PBA). All the subjects were non-smokers. Maximal expiratory flow-volume (MEFV) curves were visually classified into five types (A-E). The percent distribution of type A in healthy subjects was significantly higher than in the PNA group, while the total sum of percentage of types B, C, and D in the PNA group was significantly higher than in the healthy subjects. The percent distribution of type E in the PNA group was similar to that in the healthy subjects. The percent distribution of MEFV types were significantly different between healthy males and healthy females. The percent distribution of types A, B and E were the highest in healthy subjects, PNA and PBA groups, respectively. Conclusively, the difference in the percent distributions of MEFV types was recognized among healthy subjects, PNA and PBA groups. |
| キーワード | maximal expiratory flow-volme type non-smoking bronchial asthma nasal allergy |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 29 |
| 終了ページ | 35 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 2063693 |
| Web of Science KeyUT | A1991FA75000004 |
| JaLCDOI | 10.18926/AMO/32218 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Matsuo, Shinji| Neya, Toshiaki| Yamasato, Teruhiro| |
| 抄録 | Antroduodenal contractions were studied in rat preparations. Augmented duodenal contractions occurred spontaneously in coordination with antral contractions in normal and saline-pretreated preparations. The coordination did not occur when muscle layers and the myenteric plexus were transversely cut at the duodenum just anal to the gastroduodenal junction. In silent preparations, the coordinated contractions were produced by neostigmine or domperidone. When the antroduodenal junctional zone was pretreated with benzalkonium chloride, the augmented duodenal contractions did not occur spontaneously, and even after administration of neostigmine and domperidone although antral contractions occurred spontaneously. In these preparations, there were notably few myenteric neurons in the junctional zone, but the neurons were distributed normally in the areas where motility was recorded. The results suggest that myenteric neurons mediate antroduodenal coordinated contractions and that the coordination is modified by myenteric cholinergic excitatory and dopaminergic inhibitory pathways. |
| キーワード | gastroduodenal motility coordinated contraction myenteric plexus rat |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 21 |
| 終了ページ | 27 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 2063692 |
| Web of Science KeyUT | A1991FA75000003 |
| JaLCDOI | 10.18926/AMO/32217 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Usai, Yoshiyuki| Sasaki, Sumiji| Hirai, Ryuji| Kishi, Atsuhiko| |
| 抄録 | Post-traumatic colonic stenosis (obstruction) is rare. We experienced a case of sigmoid obstruction due to blunt abdominal trauma. A 75-year-old man was hit on the lower abdomen 3 days before admission and gradually developed abdominal pain and distension. Laboratory data showed severe inflammation and a barium enema disclosed obstruction of the sigmoid colon. Conservative treatment was carefully carried out, because there was no sign of peritoneal irritation and there were passages of normal stool and flatus. The sigmoid obstruction gradually improved and the stenosis was almost undetectable on a barium enema on the 51st hospital day. An abdominal contusion is the most likely causal factor in this case. Compression of the sigmoid colon between the abdominal wall and the promontory of the pelvis is the most possible explanation.</P> |
| キーワード | blunt abdominal trauma colon obstruction |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 61 |
| 終了ページ | 66 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 2063697 |
| Web of Science KeyUT | A1991FA75000009 |
| JaLCDOI | 10.18926/AMO/32216 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Konobe, Takeo| Ishikawa, Nobuyoshi| Gohda, Hideo| Fukai, Konosuke| Okabe, Akinobu| |
| 抄録 | The hepatitis B virus surface antigen containing the preS2 nine amino acid sequence produced by a recombinant Saccharomyces cerevisiae (yHBsAg) was purified and its physicochemical properties were determined. Ultrastructurally, the yHBsAg was found to be a homogeneous spherical particle with a diameter of 24 +/- 4 nm. The homogeneity of the yHBsAg particles was also demonstrated by analyses of their buoyant density and isoelectric point. They consisted of protein (53%), lipid (36%) and carbohydrate (11%), and the alpha-helix content was estimated to be 32%, differing from the reported values for human plasma-derived HBsAg (hHBsAg). Immunodiffusion analysis showed that the antigenic specificity of yHBsAg was identical to that of hHBsAg. Immunization of mice demonstrated that the immunogenicity of the yHBsAg was significantly higher than that of hHBsAg. |
| キーワード | hepatitis B surface antigen yeast Pre S2 immunogenicity recombinant yeast |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 11 |
| 終了ページ | 19 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 1712147 |
| Web of Science KeyUT | A1991FA75000002 |
| JaLCDOI | 10.18926/AMO/32215 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Hayashi, Kazuhiko| Ohtsuki, Yuji| Sonobe, Hiroshi| Iwata, Jun| Furihata, Matsuo| Hikita, Tomonori| Kishino, Tatsushi| Akagi, Tadaatsu| |
| 抄録 | <p>We present a case of pre-elastofibroma-like lesion, a kind of elastic-producing fibrous tumor. The small colonic polyp, which was found in a 49-year-old asymptomatic man in association with a large colonic adenoma, showed submucosal nodular deposits of fine granular or fibrillar eosinophilic materials with interspersed fibroblastic cells. Elastic stain revealed these deposits to consist mainly of dark gray granular or partially fibrillar dense elastinophilic materials, most of which were digested with elastase. This stromal lesion somewhat resembled a pre-elastofibroma. Therefore, pre-elastofibroma-like lesions should be kept in mind as a possible origin of colonic polyp.</p> |
| キーワード | pre-elastofibroma elastic tissue colon polyp |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 49 |
| 終了ページ | 53 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 2063695 |
| Web of Science KeyUT | A1991FA75000007 |
| JaLCDOI | 10.18926/AMO/32214 |
|---|---|
| フルテキストURL | fulltext.pdf |
| 著者 | Arao, Yujiro| Hatano, Atsushi| Yamada, Masao| Uno, Fumio| Nii, Shiro| |
| 抄録 | In order to elucidate the mechanism of latent infection of herpes simplex virus (HSV), reactivatable latency of three avirulent strains (SKO-1B, -GCr Miyama, SKa) of HSV type 1 was comparatively examined in a mouse latency model. The SKO-1B strain showed high rate of virus reactivation from explanted trigeminal ganglia without n-butyrate enhancement, while the other two strains showed a very low rate of virus reactivation in the absence of n-butyrate. In the presence of n-butyrate, however, the rate of the -GCr Miyama strain jumped to a comparable level with that of SKO-1B, although the rate of SKa remained at a low level. A more precise follow-up experiment changing the virus dose highlighted the difference of the ability to reactivate from the latent state between SKO-1B and -GCr Miyama. Virus titer in trigeminal ganglia during acute phase, infectivity to cell lines of neural origin, and susceptibility to acyclovir and phosphonoacetate were assayed to know the reasons for the variation in the ability of reactivatable latency among these strains. It was concluded that the reduced infectivity to neural cells, and limited ability of reactivatable latency shown by the SKa strain could mainly be attributed to the deficiency of thymidine kinase activity.</P> |
| キーワード | herpes simplex virus type 1 neurovirulence latency reactivation n-butyrate |
| Amo Type | Article |
| 出版物タイトル | Acta Medica Okayama |
| 発行日 | 1991-02 |
| 巻 | 45巻 |
| 号 | 1号 |
| 出版者 | Okayama University Medical School |
| 開始ページ | 43 |
| 終了ページ | 47 |
| ISSN | 0386-300X |
| NCID | AA00508441 |
| 資料タイプ | 学術雑誌論文 |
| 言語 | 英語 |
| 論文のバージョン | publisher |
| 査読 | 有り |
| PubMed ID | 1648298 |
| Web of Science KeyUT | A1991FA75000006 |