SNShinichiro Nakamura

Shinichiro Nakamura

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article

Previous Organizations / Institutes

The organizations / institutes from the scholar's other articles in the past ten years


Shinichiro Nakamura has a total of 40 co-authors. Here are the top co-authors by number of shared publications:

  • Hideaki Tsuchiya

    Research Center for Animal Life Science, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Shiga 520-2192, Japan

    2 shared publications
  • Takahiro Nakagawa

    Research Center for Animal Life Science, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Shiga 520-2192, Japan

    2 shared publications
  • Akatsuki Saito

    University of Miyazaki

    1 shared publication
  • Daichi Arakawa

    Research Center for Animal Life Science, Shiga University of Medical Science, Seta Tsukinowa-cho, Otsu, Shiga 520-2192, Japan

    1 shared publication
  • F. Ono

    The Corporation for Production and Research of Laboratory Primates, Tsukuba, Ibaraki, Japan

    1 shared publication
  • H. Koie

    Department of Veterinary Medicine, College of Bioscience, Nihon University, Fujisawa, Kanagawa, Japan

    1 shared publication

Latest Publications

  • Establishment of an in vitro cytotoxicity assay platform using primary monkey cardiomyocytes

    by Takuma Iguchi, Kazunori Fujimoto, Shinichiro Nakamura, Hiroyuki Kishino, Noriyo Niino, Kazuhiko Mori


  • Open Access

    Paromomycin sulfate is an effective treatment for balantidiasis in captive cynomolgus monkeys.

    by Shinichiro Nakamura, Iori Itagaki, Takahiro Nakagawa, Ikuo Kawamoto, Takahiro Asano, Daichi Arakawa, Hideaki Tsuchiya

    There are few effective antimicrobial agents against Balantidium coli infection. The effect of paromomycin sulfate (PS) against B. coli was confirmed in this study of 596 captive cynomolgus monkeys. In several trials, the minimum dose and duration of oral administration of PS were 25 mg/day for 5 + 5 days, with a 2-day withdrawal interval. To facilitate daily PS administration, pumpkin cakes supplemented with PS were made, which not only resulted in precise effects but also increased the efficiency of preparation and administration of PS by the animal care staff. No cysts or trophozoites were detected at 14 or 16 days after the last treatments. There were no obvious differences in blood and biochemical parameters between before and after administration of PS. These results indicate that PS is effective for elimination of B. coli without hematological side effects. These data could contribute to the control of microbiological pathogens during veterinary care and colony management in primate facilities.


  • Open Access

    Presence of Viral Genome in Urine and Development of Hematuria and Pathological Changes in Kidneys in Common Marmoset (Callithrix jacchus) after Inoculation with Dengue Virus

    by Meng Ling Moi, Tsutomu Omatsu, Takanori Hirayama, Shinichiro Nakamura, Yuko Katakai, Tomoyuki Yoshida, Akatsuki Saito, Shigeru Tajima, Mikako Ito, Tomohiko Takasaki, et al.

    Common marmosets (Callithrix jacchus) developed high levels of viremia, clinical signs including fever, weight loss, a decrease in activity and hematuria upon inoculation with dengue virus (DENV). Presence of DENV genome in urine samples and pathological changes in kidneys were examined in the present study. Levels of DENV genome were determined in 228 urine samples from 20 primary DENV-inoculated marmosets and in 56 urine samples from four secondary DENV-inoculated marmosets. DENV genome was detected in 75% (15/20) of marmosets after primary DENV infection. No DENV genome was detected in urine samples from the marmosets with secondary infection with homologous DENV (0%, 0/4). Two marmosets demonstrated hematuria. Pathological analysis of the kidneys demonstrated non-suppressive interstitial nephritis with renal tubular regeneration. DENV antigen-positive cells were detected in kidneys. In human dengue virus infections, some patients present renal symptoms. The results indicate that marmosets recapitulate some aspects of the involvement of kidneys in human DENV infection, and suggest that marmosets are potentially useful for the studies of the pathogenesis of DENV infection, including kidneys.


  • Open Access

    Epidemiology of Hepatitis E Virus in Indoor-Captive Cynomolgus Monkey Colony

    by Shinichiro Nakamura, Hideaki Tsuchiya, Norio Okahara, Takahiro Nakagawa, Naomi Ohara, Hiroshi Yamamoto, Tian-Cheng Li, Naokazu Takeda, Kazumasa Ogasawara, Ryuzo Torii

    A serological survey of hepatitis E virus (HEV) antibody was conducted using 202 adult captive cynomolgus monkeys, who did not show any clinical signs of acute hepatitis. Out of these, 44 monkeys were sero-positive for anti-HEV IgG and all monkeys were negative for anti-HEV IgM. All positive monkeys came from either Vietnam or China, but none from the Philippines, Indonesia, or our facility. Selected 12 monkeys out of positive monkeys from Vietnum, including 9 positive and 3 negative, revealed mostly within the reference ranges for alanine aminotransferase (ALT) and asparatate aminotransferase (AST) by serum biochemistries. Their titers of anti-HEV IgG did not correlate with the concentrations of ALT and AST. Moreover, HEV-RNA could not be detected from any fecal specimens of the 12 monkeys. Thus, monkeys with anti-HEV IgG sero-positive did not seem to be source of the HEV-pollution, because 1) sero-positive monkeys did not excrete HEV-RNA from their feces, and 2) monkeys from the Philippines and Indonesia have remained to be sero-negative for anti-HEV IgG, even if the monkeys were kept in same animal room of our facility. From these results, it could be inferred that primary infection of HEV occurred in the exported countries, but not in our colony. The contamination of HEV in indoor-captive monkeys could be prevented by precise quarantine tests, including ELISA for detecting anti-HEV and RT-PCR for HEV RNA.


  • Open Access

    Transthyretin Amyloidosis in Aged Vervet Monkeys, as a Candidate for the Spontaneous Animal Model of Senile Systemic Amyloidosis

    by Shinichiro Nakamura, Mitsuharu Ueda, Naohide Ageyama, Yukio Ando, Ryuzo Torii

  • Open Access

    Transthyretin Amyloidosis and Two Other Aging-Related Amyloidoses in an Aged Vervet Monkey

    by S. Nakamura, S. Okabayashi, N. Ageyama, H. Koie, T. Sankai, F. Ono, K. Fujimoto, K. Terao

    An aged male vervet monkey showed severe cardiac arrhythmia for more than 3 years. A multifocal amyloid consisting of transthyretin was deposited in all areas of the heart wall, especially in the extracellular stroma among muscle fibers and external tunica of arterioles. Moreover, the amyloid was deposited in the stroma and arterioles of other systemic organs except the liver and spleen. These characteristics are consistent with senile systemic amyloidosis in humans. A second amyloid consisting of amyloid β protein was in senile plaques and cerebral amyloid angiopathy in the cerebral cortex. A third amyloid consisting of islet amyloid polypeptide was deposited in islets of the pancreas. Apolipoprotein E and amyloid P component colocalized with the 3 amyloids. Thus, 3 different aging-related amyloids were found in an aged vervet monkey. In particular, to our knowledge, this is the first report on spontaneous transthyretin amyloidosis in animals.