著者

LARRY J. YOUNG QI ZHANG

出版者

THE JAPANESE SOCIETY FOR ANIMAL PSYCHOLOGY

雑誌

動物心理学研究 (ISSN:09168419)

巻号頁・発行日

pp.71.1.4, (Released:2021-05-17)

参考文献数

87

被引用文献数

9

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Here we discuss the origins of diversity in social behavior by highlighting research using the socially monogamous prairie vole. Prairie voles display a rich social behavioral repertoire involving pair bonding and consoling behavior that are not observed in typical laboratory species. Oxytocin and vasopressin play critical roles in regulating pair bonding and consoling behavior. Oxytocin and vasopressin receptors show remarkable diversity in expression patterns both between and within species. Receptor expression patterns are associated with species differences in social behaviors. Variations in receptor genes have been linked to individual variation in expression patterns. We propose that "evolvability" in the oxytocin and vasopressin receptor genes allows for the repurposing of ancient maternal and territorial circuits to give rise to novel social behaviors such as pair bonding, consoling and selective aggression. We further propose that the evolvability of these receptor genes is due to their transcriptional sensitivity to genomic variation. This model provides a foundation for investigating the molecular mechanisms giving rise to the remarkable diversity in social behaviors found in vertebrates.

著者

Bao-Juan Cui Dao-Qing Wang Jian-Qing Qiu Lai-Gang Huang Fan-Shuo Zeng Qi Zhang Min Sun Ben-Ling Liu Qiang-San Sun

出版者

理学療法科学学会

雑誌

Journal of Physical Therapy Science (ISSN:09155287)

巻号頁・発行日

vol.27, no.7, pp.2327-2331, 2015 (Released:2015-07-22)

参考文献数

18

被引用文献数

1 6

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[Purpose] This study investigated the effects of a 12-hour neuromuscular electrical stimulation program in the evening hours on upper extremity function in sub-acute stroke patients. [Subjects and Methods] Forty-five subjects were randomized to one of three groups: 12-hour neuromuscular electrical stimulation group (n=15), which received 12 hours of neuromuscular electrical stimulation and conventional rehabilitation for the affected upper extremity; neuromuscular electrical stimulation group (n=15), which received 30 min of neuromuscular electrical stimulation and conventional rehabilitation; and control group (n=15), which received conventional rehabilitation only. The Fugl-Meyer assessment, Action Research Arm Test, and modified Ashworth scale were used to evaluate the effects before and after intervention, and 4 weeks later. [Results] The improvement in the distal (wrist-hand) components of the Fugl-Meyer assessment and Action Research Arm Test in the 12-hour neuromuscular electrical stimulation group was more significant than that in the neuromuscular electrical stimulation group. No significant difference was found between the two groups in the proximal component (shoulder-elbow) of the Fugl-Meyer assessment. [Conclusion] The 12-hour neuromuscular electrical stimulation group achieved better improvement in upper extremity motor function, especially in the wrist-hand function. This alternative therapeutic approach is easily applicable and can be used in stroke patients during rest or sleep.

著者

Qi Zhang Peizheng Yan Pan Zhao Dongsheng Zhao Heran Cao Jing Lu Beibei Mao

出版者

The Pharmaceutical Society of Japan

雑誌

Chemical and Pharmaceutical Bulletin (ISSN:00092363)

巻号頁・発行日

vol.71, no.2, pp.120-128, 2023-02-01 (Released:2023-02-01)

参考文献数

35

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Mechanistic target of rapamycin (mTOR) is an effective anti-tumor drug target. Several mTOR kinase inhibitors have entered clinical research, but there are still challenges of potential toxicity. As a new type of targeted drug, proteolysis targeting chimeras (PROTACs) have features of low dosage and low toxicity. However, this approach has been rarely reported to involve mTOR degradation. In this study, the mTOR kinase inhibitor MLN0128 was used as the ligand to the protein of interest and conjugated with pomalidomide by diverse intermediate linkage chains. Several potential small molecule PROTACs for the degradation of mTOR were designed and synthesized. PROTAC compounds exhibited mTOR inhibitory activity and suppressed MCF-7 cell proliferation. The representative compound P1 could inhibit the expression of mTOR downstream proteins and the growth of cancer cells by inducing autophagy but not affecting the cell cycle and not inducing apoptosis.

著者

Yu Wei Sun Xin Yu Wang Lu Liu Qi Zhang Yong Jing Xi Pi Wu Wang

出版者

Japanese Society of Breeding

雑誌

Breeding Science (ISSN:13447610)

巻号頁・発行日

vol.73, no.3, pp.290-299, 2023 (Released:2023-07-27)

参考文献数

44

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Light provides energy for photosynthesis and is also an important environmental signal that regulates plant growth and development. Ribose-5-phosphate isomerase plays a crucial role in photosynthesis. However, ribose-5-phosphate isomerase has yet to be studied in soybean photosynthesis. To understand the biological function of GmRPI2, in this study, GmRPI2 was cloned, plant overexpression vectors and gene editing vectors were successfully constructed, and transformed into recipient soybean JN74 using the Agrobacterium-mediated method. Using qRT-PCR, we analyzed that GmRPI2 gene expression was highest in leaves, second highest in roots, and lowest in stems. Promoter analysis revealed the presence of multiple cis-acting elements related to light response in the promoter region of GmRPI2. Compared with the control soybean plants, the net photosynthetic rate and transpiration rate of the overexpression lines were higher than those of the control and gene editing lines, while the intercellular CO2 concentration was significantly lower than that of the control and gene editing lines; the total chlorophyll, chlorophyll a, chlorophyll b contents and soluble sugar contents of the overexpression plants were significantly higher than those of the recipient and editing plants, indicating that the GmRPI2 gene can increase The GmRPI2 gene can increase the photosynthetic capacity of soybean plants, providing a theoretical basis and genetic resources for improving soybean yield by regulating photosynthetic efficiency.

著者

Hangjin SUN Lei WANG Zhaoyang QIU Qi ZHANG

出版者

The Institute of Electronics, Information and Communication Engineers

雑誌

IEICE TRANSACTIONS on Fundamentals of Electronics, Communications and Computer Sciences (ISSN:09168508)

巻号頁・発行日

vol.E105-A, no.12, pp.1616-1620, 2022-12-01

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The Nyquist folding receiver (NYFR) is a novel analog-to-information architecture, which can achieve wideband receiving with a small amount of system resource. The NYFR uses a radio frequency (RF) non-uniform sampling to realize wideband receiving, and the practical RF non-uniform sample pulse train usually contains an aperture. Therefore, it is necessary to investigate the aperture impact on the NYFR output. In this letter, based on the NYFR output signal to noise ratio (SNR), the aperture impact on the NYFR is analyzed. Focusing on the aperture impact, the corresponding NYFR output signal power and noise power are given firstly. Then, the relation between the aperture and the output SNR is analyzed. In addition, the output SNR distribution containing the aperture is investigated. Finally, combing with a parameter estimation method, several simulations are conducted to prove the theoretical aperture impact.

著者

Qi Zhang Peizheng Yan Pan Zhao Dongsheng Zhao Heran Cao Jing Lu Beibei Mao

出版者

The Pharmaceutical Society of Japan

雑誌

Chemical and Pharmaceutical Bulletin (ISSN:00092363)

巻号頁・発行日

pp.c22-00576, (Released:2022-11-26)

参考文献数

35

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mTOR is an effective anti-tumor drug target. Several mTOR kinase inhibitors have entered clinical research, but there are still challenges of potential toxicity. As a new type of targeted drug, proteolysis targeting chimeras (PROTACs) have features of low dosage and low toxicity. However, this approach has been rarely reported to involve mTOR degradation. In this study, the mTOR kinase inhibitor MLN0128 was used as the ligand to the protein of interest and conjugated with pomalidomide by diverse intermediate linkage chains. Several potential small molecule PROTACs for the degradation of mTOR were designed and synthesized. PROTAC compounds exhibited mTOR inhibitory activity and suppressed MCF-7 cell proliferation. The representative compound P1 could inhibit the expression of mTOR downstream proteins and the growth of cancer cells by inducing autophagy but not affecting the cell cycle and not inducing apoptosis.