The Tsushima leopard cat exhibits extremely low genetic diversity compared with the Korean Amur leopard cat: Implications for conservation

We examined genetic diversity of the wild Tsushima leopard cat—a regional population of the Amur leopard cat—using microsatellite markers. In addition, we compared genetic diversity of the Tsushima leopard cat with that of the Korean population of Amur leopard cat. Although bias should be considered when applying cross-species amplification, the Tsushima leopard cat showed a lower index of molecular genetic diversity than did the Korean population. These results were consistent with those obtained using other genetic markers, such as mitochondrial DNA and Y chromosome sequences. This low genetic diversity of the wild Tsushima leopard cat may be derived from the founding population. Furthermore, our results suggest that the captive populations held in Japanese zoos may show extremely low genetic diversity, leading to difficulties in genetic management of the Tsushima leopard cat. Moreover, the two regional populations were clearly separated using these marker sets. In the present study, we demonstrated that the genetic diversity of the Tsushima leopard cat is extremely low compared with that of the continental regional population. Importantly, the Japanese captive population for ex situ conservation was derived from a founding population with extremely low genetic diversity; hence, we assume that both the captive and wild populations showed extremely low genetic diversities. Our findings emphasize the need to develop carefully considered management strategies for genetic conservation

Preparation of New Nitrogen-Bridged Heterocycles. 34. Synthesis and Reaction of 2,3-Dihydrooxepino [2,3-b]-indolizines

Article信州大学工学部紀要 74: 31-42 (1994)departmental bulletin pape

Study on networking issues of medium earth orbit satellite communications systems

Two networking issues of communications systems with medium earth orbit (MEO) satellites, namely network architectures and location determination and registration methods for hand-held terminals, are investigated in this paper. For network architecture, five candidate architectures are considered and evaluated in terms of signaling traffic. For location determination and registration, two methods are discussed and evaluated

Preparation of New Nitrogen-bridged Heterocycles. 12. Reaction of 2-(Acylmethoxy)-3-vinylindolizines in the Presence of a Base

Article信州大学工学部紀要 58: 1-8 (1985)departmental bulletin pape

Potential Antitumor Activity of 2-O-α-D-Glucopyranosyl-6-O-(2-Pentylheptanoyl)-L-Ascorbic Acid

Intravenous administration of high-dose ascorbic acid (AA) has been reported as a treatment for cancer patients. However, cancer patients with renal failure cannot receive this therapy because high-dose AA infusion can have side effects. To solve this problem, we evaluated the antitumor activity of a lipophilic stable AA derivative, 2-O-α-D-glucopyranosyl-6-O-(2-pentylheptanoyl)-L-ascorbic acid (6-bOcta-AA-2G). Intravenous administration of 6-bOcta-AA-2G suppressed tumor growth in colon-26 tumor-bearing mice more strongly than did AA, even at 1/10 of the molar amount of AA. Experiments on the biodistribution and clearance of 6-bOcta-AA-2G and its metabolites in tumor-bearing mice showed that 6-bOcta-AA-2G was hydrolyzed to 6-O-(2-propylpentanoyl)-L-ascorbic acid (6-bOcta-AA) slowly to yield AA, and the results suggested that this characteristic metabolic pattern is responsible for making the antitumor activity of 6-bOcta-AA-2G stronger than that of AA and that the active form of 6-bOcta-AA-2G showing antitumor activity is 6-bOcta-AA. In in vitro experiments, the oxidized form of 6-bOcta-AA as well as 6-bOcta-AA showed significant cytotoxicity, while the oxidized forms of ascorbic acid showed no cytotoxicity at all, suggesting that the antitumor activity mechanism of 6-bOcta-AA-2G is different from that of AA and that the antitumor activity is due to the reduced and oxidized form of 6-bOcta-AA. The findings suggest that 6-bOcta-AA-2G is a potent candidate as an alternative drug to intravenous high-dose AA

Effect of 1,2-Dimethylhydrazine and Hydrogen Peroxide for the Duodenal Tumorigenesis in Relation to Blood Catalase Activity in Mice

Three different mouse strains, C3H/C^b_s C3H/HeN and B6C3 (C57BL x C3H) F1, having low, high and moderate catalase activities, were studied for duodenal tumorigenesis by the combined treatment with 1,2-dimethylhydrazine (DMH)* and hydrogen peroxide (HPO). DMH alone rarely induced duodenal tumors. Administration of HPO into 3 different mouse strains induced different frequencies of duodenal tumors ; 91.7% in C3H/C^b_s 9.5% in C3H/HeN and 31.8% in B6C3F1 mice. The incidence of duodenal tumors was significantly increased to 52.6% and 93.8% both in C3H/HeN and B6C3F1 mice by the combined administration of DMH and HPO. These increases in duodenal tumor were inversely correlated with the finding that administration of DMH or HPO alone or combined treatment of DMH and HPO significantly decreased mean blood catalase activities both in C3H and B6C3F1 mice