Argipressin (BioDeep_00001028386)

Main id: BioDeep_00000009494

 


代谢物信息卡片


8-L-Arginine vasopressin

化学式: C46H65N15O12S2 (1083.437833)
中文名称: 精氨酸加压素
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1CC(N(C1)C(=O)C2CSSCC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2)CC(=O)N)CCC(=O)N)CC3=CC=CC=C3)CC4=CC=C(C=C4)O)N)C(=O)NC(CCCN=C(N)N)C(=O)NCC(=O)N
InChI: InChI=1S/C46H65N15O12S2/c47-27-22-74-75-23-33(45(73)61-17-5-9-34(61)44(72)56-28(8-4-16-53-46(51)52)39(67)54-21-37(50)65)60-43(71)32(20-36(49)64)59-40(68)29(14-15-35(48)63)55-41(69)31(18-24-6-2-1-3-7-24)58-42(70)30(57-38(27)66)19-25-10-12-26(62)13-11-25/h1-3,6-7,10-13,27-34,62H,4-5,8-9,14-23,47H2,(H2,48,63)(H2,49,64)(H2,50,65)(H,54,67)(H,55,69)(H,56,72)(H,57,66)(H,58,70)(H,59,68)(H,60,71)(H4,51,52,53)/t27-,28-,29-,30-,31-,32-,33-,34-/m0/s1

描述信息

C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C80212 - Antidiuretic Hormone Analogue
D002317 - Cardiovascular Agents > D014662 - Vasoconstrictor Agents > D014667 - Vasopressins
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
D006401 - Hematologic Agents > D003029 - Coagulants > D006490 - Hemostatics
D002317 - Cardiovascular Agents > D045283 - Natriuretic Agents
D045283 - Natriuretic Agents > D050034 - Antidiuretic Agents
Same as: D00101
Argipressin (Arg8-vasopressin) binds to the V1, V2, V3-vascular arginine vasopressin receptor, with a Kd value of 1.31 nM in A7r5 rat aortic smooth muscle cells for V1.

同义名列表

6 个代谢物同义名

8-L-Arginine vasopressin; Arg-vasopressin; Argipressin; ADH; AVP; Arg8-vasopressin



数据库引用编号

10 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

0 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。



文献列表

  • Yexiu Sun, Ying Guo, He Xu, Ji Zhao, Di Wu, Jianwei Hu, Dandan Wang, Lei Wu, Hao Peng, Hongmei Li. The relationship between arginine vasopressin gene polymorphisms and plasma copeptin and hypertensive disorders of pregnancy: a nested case-control study. Journal of hypertension. 2023 04; 41(4):608-617. doi: 10.1097/hjh.0000000000003376. [PMID: 36723473]
  • Kota Kakeshita, Tsutomu Koike, Teruhiko Imamura, Hayato Fujioka, Hidenori Yamazaki, Koichiro Kinugawa. Altered arginine vasopressin-cyclic AMP-aquaporin 2 pathway in patients with chronic kidney disease. Clinical and experimental nephrology. 2022 Aug; 26(8):788-796. doi: 10.1007/s10157-022-02220-1. [PMID: 35503490]
  • Xinqi Jiang, Tao Lu, Yihang Dong, Jiaru Shi, Mengyao Duan, Xiaoqing Zhang. Effectiveness and safety of moxibustion for vascular dementia: A systematic review and meta-analysis. Medicine. 2022 Jul; 101(26):e29804. doi: 10.1097/md.0000000000029804. [PMID: 35777054]
  • Ana Lavedán Santamaría, Olga Masot, Olga Canet Velez, Teresa Botigué, Tània Cemeli Sánchez, Judith Roca. Diagnostic Concordance between the Visual Analogue Anxiety Scale (VAS-A) and the State-Trait Anxiety Inventory (STAI) in Nursing Students during the COVID-19 Pandemic. International journal of environmental research and public health. 2022 Jun; 19(12):. doi: 10.3390/ijerph19127053. [PMID: 35742303]
  • Ye-Ji Kim, Jei Ha Lee, Seung-Hyun Jung, Ki Hyun Kim, Chang-Hoon Choi, Seonmi Jo, Dong Ho Woo. An Octopus-Derived Peptide with Antidiuretic Activity in Rats. Marine drugs. 2022 May; 20(5):. doi: 10.3390/md20050328. [PMID: 35621979]
  • Hiroyuki Arakawa, Yuki Higuchi. Exocrine scent marking: Coordinative role of arginine vasopressin in the systemic regulation of social signaling behaviors. Neuroscience and biobehavioral reviews. 2022 05; 136(?):104597. doi: 10.1016/j.neubiorev.2022.104597. [PMID: 35248677]
  • Pedro Alves Soares Vaz de Castro, Letícia Bitencourt, Juliana Lacerda de Oliveira Campos, Bruna Luisa Fischer, Stephanie Bruna Camilo Soares de Brito, Beatriz Santana Soares, Juliana Beaudette Drummond, Ana Cristina Simões E Silva. Nephrogenic diabetes insipidus: a comprehensive overview. Journal of pediatric endocrinology & metabolism : JPEM. 2022 Apr; 35(4):421-434. doi: 10.1515/jpem-2021-0566. [PMID: 35146976]
  • Danni Mu, Chaochao Ma, Jin Cheng, Yutong Zou, Ling Qiu, Xinqi Cheng. Copeptin in fluid disorders and stress. Clinica chimica acta; international journal of clinical chemistry. 2022 Apr; 529(?):46-60. doi: 10.1016/j.cca.2022.02.002. [PMID: 35143773]
  • Kenya Sanada, Hiromichi Ueno, Tetsu Miyamoto, Kazuhiko Baba, Kentaro Tanaka, Haruki Nishimura, Kazuaki Nishimura, Satomi Sonoda, Mitsuhiro Yoshimura, Takashi Maruyama, Tatsushi Onaka, Yutaka Otsuji, Masaharu Kataoka, Yoichi Ueta. AVP-eGFP was significantly upregulated by hypovolemia in the parvocellular division of the paraventricular nucleus in the transgenic rats. American journal of physiology. Regulatory, integrative and comparative physiology. 2022 03; 322(3):R161-R169. doi: 10.1152/ajpregu.00107.2021. [PMID: 35018823]
  • Sapna Ramdin, Thajasvarie Naicker, Virushka Pillay, Sanil D Singh, Sooraj Baijnath, Blessing N Mkhwanazi, Nalini Govender. Physiological characterization of an arginine vasopressin rat model of preeclampsia. Systems biology in reproductive medicine. 2022 Feb; 68(1):55-69. doi: 10.1080/19396368.2021.1981486. [PMID: 34743622]
  • Lucia Sugawara, Takaaki Nakamura, Yoshitaka Ishizuka, Hiroshi Maegawa. A case of central diabetes insipidus due to neurophysin II gene abnormality diagnosed based on a family history of nocturnal enuresis. Endocrine journal. 2022 Jan; 69(1):95-100. doi: 10.1507/endocrj.ej21-0187. [PMID: 34544934]
  • Arno Téblick, Lauren De Bruyn, Tim Van Oudenhove, Sarah Vander Perre, Lies Pauwels, Sarah Derde, Lies Langouche, Greet Van den Berghe. Impact of Hydrocortisone and of CRH Infusion on the Hypothalamus-Pituitary-Adrenocortical Axis of Septic Male Mice. Endocrinology. 2022 01; 163(1):. doi: 10.1210/endocr/bqab222. [PMID: 34698826]
  • R C Dos-Santos, T Vilhena-Franco, L C Reis, L L K Elias, J Antunes-Rodrigues, A S Mecawi. AMPA and angiotensin type 1 receptors are necessary for hemorrhage-induced vasopressin secretion. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas. 2022; 55(?):e11635. doi: 10.1590/1414-431x2021e11635. [PMID: 35137852]
  • Jinshan Wang, Shizhen Jin, Wenshuang Fu, Yufeng Liang, Yani Yang, Xiaohong Xu. Pubertal exposure to bisphenol-A affects social recognition and arginine vasopressin in the brain of male mice. Ecotoxicology and environmental safety. 2021 Dec; 226(?):112843. doi: 10.1016/j.ecoenv.2021.112843. [PMID: 34601267]
  • Masanori Nakata, Parmila Kumari, Rika Kita, Nanako Katsui, Yuriko Takeuchi, Tomoki Kawaguchi, Toshiya Yamazaki, Boyang Zhang, Shigeki Shimba, Toshihiko Yada. Circadian Clock Component BMAL1 in the Paraventricular Nucleus Regulates Glucose Metabolism. Nutrients. 2021 Dec; 13(12):. doi: 10.3390/nu13124487. [PMID: 34960038]
  • Angela Kim, Jakob G Knudsen, Joseph C Madara, Anna Benrick, Thomas G Hill, Lina Abdul Kadir, Joely A Kellard, Lisa Mellander, Caroline Miranda, Haopeng Lin, Timothy James, Kinga Suba, Aliya F Spigelman, Yanling Wu, Patrick E MacDonald, Ingrid Wernstedt Asterholm, Tore Magnussen, Mikkel Christensen, Tina Vilsbøll, Victoria Salem, Filip K Knop, Patrik Rorsman, Bradford B Lowell, Linford Jb Briant. Arginine-vasopressin mediates counter-regulatory glucagon release and is diminished in type 1 diabetes. eLife. 2021 11; 10(?):. doi: 10.7554/elife.72919. [PMID: 34787082]
  • Hayder M Al-Kuraishy, Ali I Al-Gareeb, Safaa Qusti, Eida M Alshammari, Francis O Atanu, Gaber El-Saber Batiha. Arginine vasopressin and pathophysiology of COVID-19: An innovative perspective. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2021 Nov; 143(?):112193. doi: 10.1016/j.biopha.2021.112193. [PMID: 34543987]
  • Shruti Mohan, Peter R Flatt, Nigel Irwin, R Charlotte Moffett. Weight-reducing, lipid-lowering and antidiabetic activities of a novel arginine vasopressin analogue acting at the V1a and V1b receptors in high-fat-fed mice. Diabetes, obesity & metabolism. 2021 10; 23(10):2215-2225. doi: 10.1111/dom.14462. [PMID: 34105240]
  • Shigeki Yokoyama, Teruhiko Imamura, Shigeyuki Yamashita, Toshio Doi, Kazuaki Fukahara, Naoki Yoshimura, Koichiro Kinugawa. Peak Lag Between Plasma Vasopressin and Urine Aquaporin-2 Following Cardiac Surgery. International heart journal. 2021 Sep; 62(5):1057-1061. doi: 10.1536/ihj.21-301. [PMID: 34544990]
  • Daniele T Alves, Luiz Felipe Mendes, Walkyria O Sampaio, Leda M C Coimbra-Campos, Maria Aparecida R Vieira, Anderson J Ferreira, Almir S Martins, Elena Popova, Mihail Todiras, Fatimunnisa Qadri, Natalia Alenina, Michael Bader, Robson A S Santos, Maria Jose Campagnole-Santos. Hemodynamic phenotyping of transgenic rats with ubiquitous expression of an angiotensin-(1-7)-producing fusion protein. Clinical science (London, England : 1979). 2021 09; 135(18):2197-2216. doi: 10.1042/cs20210599. [PMID: 34494083]
  • Angela Kim, Joseph C Madara, Chen Wu, Mark L Andermann, Bradford B Lowell. Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality. eLife. 2021 09; 10(?):. doi: 10.7554/elife.66609. [PMID: 34585668]
  • Masaki Takiwaki, Fumio Nomura, Mamoru Satoh, Sachio Tsuchida, Kazuo Otake, Junko Takagi. Development of a sensitive liquid chromatography-tandem mass spectrometry method for quantification of human plasma arginine vasopressin. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2021 Sep; 1181(?):122903. doi: 10.1016/j.jchromb.2021.122903. [PMID: 34455342]
  • Annette Hus-Citharel, Nadine Bouby, Maithé Corbani, Julie Mion, Christiane Mendre, Judit Darusi, Csaba Tomboly, Miguel Trueba, Claudine Serradeil-Le Gal, Catherine Llorens-Cortes, Gilles Guillon. Characterization of a functional V1B vasopressin receptor in the male rat kidney: evidence for cross talk between V1B and V2 receptor signaling pathways. American journal of physiology. Renal physiology. 2021 09; 321(3):F305-F321. doi: 10.1152/ajprenal.00081.2021. [PMID: 34282956]
  • Xiangyan Jin, Woong Bin Kim, Mi-Na Kim, Won Woo Jung, Hyung Kyung Kang, Eun-Hwa Hong, Yoon Sik Kim, Wan Joo Shim, Hee Chul Han, Christopher S Colwell, Young-Beom Kim, Yang In Kim. Oestrogen inhibits salt-dependent hypertension by suppressing GABAergic excitation in magnocellular AVP neurons. Cardiovascular research. 2021 08; 117(10):2263-2274. doi: 10.1093/cvr/cvaa271. [PMID: 32960965]
  • Mitsuhiro Yoshimura, Becky Conway-Campbell, Yoichi Ueta. Arginine vasopressin: Direct and indirect action on metabolism. Peptides. 2021 08; 142(?):170555. doi: 10.1016/j.peptides.2021.170555. [PMID: 33905792]
  • Jack Whylings, Nicole Rigney, Geert J de Vries, Aras Petrulis. Reduction in vasopressin cells in the suprachiasmatic nucleus in mice increases anxiety and alters fluid intake. Hormones and behavior. 2021 07; 133(?):104997. doi: 10.1016/j.yhbeh.2021.104997. [PMID: 34062279]
  • Johannes Leierer, Paul Perco, Benedikt Hofer, Susanne Eder, Alexander Dzien, Julia Kerschbaum, Michael Rudnicki, Gert Mayer. Coregulation Analysis of Mechanistic Biomarkers in Autosomal Dominant Polycystic Kidney Disease. International journal of molecular sciences. 2021 Jun; 22(13):. doi: 10.3390/ijms22136885. [PMID: 34206927]
  • Daisuke Hagiwara, Masayoshi Tochiya, Yoshinori Azuma, Tetsuro Tsumura, Yuichi Hodai, Yohei Kawaguchi, Takashi Miyata, Tomoko Kobayashi, Mariko Sugiyama, Takeshi Onoue, Hiroshi Takagi, Yoshihiro Ito, Shintaro Iwama, Hidetaka Suga, Ryoichi Banno, Hiroshi Arima. Arginine vasopressin-Venus reporter mice as a tool for studying magnocellular arginine vasopressin neurons. Peptides. 2021 05; 139(?):170517. doi: 10.1016/j.peptides.2021.170517. [PMID: 33647312]
  • Balázs Mayer, Krisztián Németh, Miklós Krepuska, Vamsee D Myneni, Dragan Maric, John F Tisdale, Matthew M Hsieh, Naoya Uchida, Heon-Jin Lee, Michael J Nemeth, Kenn Holmbeck, Constance Tom Noguchi, Heather Rogers, Soumyadeep Dey, Arne Hansen, Jeffrey Hong, Ian Chow, Sharon Key, Ildikó Szalayova, Jerome Pagani, Károly Markó, Ian MacClain-Caldwell, Lynn Vitale-Cross, W Scott Young, Michael J Brownstein, Éva Mezey. Commentary on Winzeler et al 'Low arginine vasopressin levels in patients with diabetes insipidus are not associated with anaemia'. Clinical endocrinology. 2021 05; 94(5):888-890. doi: 10.1111/cen.14377. [PMID: 33314284]
  • Raj Makwana, John Loy, Miriam Adebibe, Kalpana Devalia, Paul Lr Andrews, Gareth J Sanger. Copeptin, a surrogate marker of arginine8 vasopressin, has no ability to modulate human and mouse gastric motility. European journal of pharmacology. 2021 Feb; 892(?):173740. doi: 10.1016/j.ejphar.2020.173740. [PMID: 33220268]
  • Adrien Flahault, Pierre-Emmanuel Girault-Sotias, Mathilde Keck, Rodrigo Alvear-Perez, Nadia De Mota, Lucie Estéoulle, Sridévi M Ramanoudjame, Xavier Iturrioz, Dominique Bonnet, Catherine Llorens-Cortes. A metabolically stable apelin-17 analog decreases AVP-induced antidiuresis and improves hyponatremia. Nature communications. 2021 01; 12(1):305. doi: 10.1038/s41467-020-20560-y. [PMID: 33436646]
  • Konstantinos Kamperis. Nocturnal enuresis in children: The role of arginine-vasopressin. Handbook of clinical neurology. 2021; 181(?):289-297. doi: 10.1016/b978-0-12-820683-6.00021-x. [PMID: 34238464]
  • Martín Muñoz-Ortega, Noé Macías-Segura, Javier Ventura-Juárez, Manuel Enrique Ávila-Blanco, Leonardo D Ponce-Damian, Daniel González-Blas, Esperanza Sánchez-Alemán, Andrés Quintanar-Stephano. Recovery from Liver Failure and Fibrosis in a Rat Portacaval Anastomosis Model after Neurointermediate Pituitary Lobectomy. Journal of immunology research. 2021; 2021(?):5529784. doi: 10.1155/2021/5529784. [PMID: 34926704]
  • Dong Hee Kim, Kwang Kon Kim, Tae Hwan Lee, Hyejin Eom, Jin Woo Kim, Jeong Woo Park, Jin Kwon Jeong, Byung Ju Lee. Transcription Factor TonEBP Stimulates Hyperosmolality-Dependent Arginine Vasopressin Gene Expression in the Mouse Hypothalamus. Frontiers in endocrinology. 2021; 12(?):627343. doi: 10.3389/fendo.2021.627343. [PMID: 33796071]
  • Hanna Szmygin, Joanna Szydełko, Beata Matyjaszek-Matuszek. Copeptin as a novel biomarker of cardiometabolic syndrome. Endokrynologia Polska. 2021; 72(5):566-571. doi: 10.5603/ep.a2021.0072. [PMID: 34378786]
  • Vallari Kothari, Zulma Cardona, Yuval Eisenberg. Adipsic diabetes insipidus. Handbook of clinical neurology. 2021; 181(?):261-273. doi: 10.1016/b978-0-12-820683-6.00019-1. [PMID: 34238462]
  • Kirthikaa Balapattabi, Joel T Little, Martha E Bachelor, Rebecca L Cunningham, J Thomas Cunningham. Sex Differences in the Regulation of Vasopressin and Oxytocin Secretion in Bile Duct-Ligated Rats. Neuroendocrinology. 2021; 111(3):237-248. doi: 10.1159/000508104. [PMID: 32335554]
  • Pierre-Emmanuel Girault-Sotias, Nadia De Mota, Catherine Llorens-Cortès. [Physiological role of the apelin receptor: implication in body fluid homeostasis and hyponatremia]. Biologie aujourd'hui. 2021; 215(3-4):119-132. doi: 10.1051/jbio/2021012. [PMID: 35275056]
  • Jernej Jorgačevski, Robert Zorec, Maja Potokar. Insights into Cell Surface Expression, Supramolecular Organization, and Functions of Aquaporin 4 Isoforms in Astrocytes. Cells. 2020 12; 9(12):. doi: 10.3390/cells9122622. [PMID: 33297299]
  • Christopher A Lear, Michi Kasai, Paul P Drury, Joanne O Davidson, Etsuko Miyagi, Laura Bennet, Alistair J Gunn. Plasma vasopressin levels are closely associated with fetal hypotension and neuronal injury after hypoxia-ischemia in near-term fetal sheep. Pediatric research. 2020 12; 88(6):857-864. doi: 10.1038/s41390-020-0845-2. [PMID: 32179873]
  • Juliana B Drummond, Beatriz S Soares, William Pedrosa, Erica L M Vieira, Antonio L Teixeira, Mirjam Christ-Crain, Antonio Ribeiro-Oliveira. Copeptin response to hypoglycemic stress is linked to prolactin activation in children. Pituitary. 2020 Dec; 23(6):681-690. doi: 10.1007/s11102-020-01076-6. [PMID: 32851504]
  • Yue Song, Liang-Xiao Ma, Ying-Ying Gan, Jun-Xiang Wang, Jie-Dan Mu, Meng-Wei Guo, Xiao-Xuan Ren, Wen-Yan Yu, Yuan Tian, Xu Qian, Tian-Yi Sun. [Perpendicular and transverse needling of "Sanyinjiao" (SP6) relieves abdominal pain by regulating arginine vasopressin and its receptor expression levels in uterus and hypothalamus in cold-stasis type dysmenorrhea rats]. Zhen ci yan jiu = Acupuncture research. 2020 Nov; 45(11):895-901. doi: 10.13702/j.1000-0607.200184. [PMID: 33269833]
  • Yohei Kawaguchi, Daisuke Hagiwara, Takashi Miyata, Yuichi Hodai, Junki Kurimoto, Hiroshi Takagi, Hidetaka Suga, Tomoko Kobayashi, Mariko Sugiyama, Takeshi Onoue, Yoshihiro Ito, Shintaro Iwama, Ryoichi Banno, Valery Grinevich, Hiroshi Arima. Endoplasmic reticulum chaperone BiP/GRP78 knockdown leads to autophagy and cell death of arginine vasopressin neurons in mice. Scientific reports. 2020 11; 10(1):19730. doi: 10.1038/s41598-020-76839-z. [PMID: 33184425]
  • Marie-Anne Burckhardt, Verena Gotta, Svetlana Beglinger, Luzia Renggli, Sara Bachmann, Melanie Hess, Katharina Rentsch, Marc Pfister, Gilbert Koch, Elizabeth A Davis, Urs Zumsteg, Timothy W Jones, Gabor Szinnai. Copeptin Kinetics and Its Relationship to Osmolality During Rehydration for Diabetic Ketoacidosis in Children. The Journal of clinical endocrinology and metabolism. 2020 11; 105(11):. doi: 10.1210/clinem/dgaa568. [PMID: 32835363]
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  • Yi-Kyeong Jeong, Ye-In Oh, Kun-Ho Song, Kyoung Won Seo. Evaluation of salivary vasopressin as an acute stress biomarker in healthy dogs with stress due to noise and environmental challenges. BMC veterinary research. 2020 Sep; 16(1):331. doi: 10.1186/s12917-020-02555-5. [PMID: 32917190]
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  • Chunyan Hu, Jayalakshmi Lakshmipathi, Deborah Stuart, Janos Peti-Peterdi, Georgina Gyarmati, Chuan-Ming Hao, Peter Hansell, Donald E Kohan. Renomedullary Interstitial Cell Endothelin A Receptors Regulate BP and Renal Function. Journal of the American Society of Nephrology : JASN. 2020 07; 31(7):1555-1568. doi: 10.1681/asn.2020020232. [PMID: 32487560]
  • Kentaro Tanaka, Reiko Saito, Kenya Sanada, Haruki Nishimura, Kazuaki Nishimura, Satomi Sonoda, Hiromichi Ueno, Yasuhito Motojima, Takanori Matsuura, Mitsuhiro Yoshimura, Takashi Maruyama, Tatsushi Onaka, Yukiyo Yamamoto, Koichi Kusuhara, Yoichi Ueta. Expression of hypothalamic feeding-related peptide genes and neuroendocrine responses in an experimental allergic encephalomyelitis rat model. Peptides. 2020 07; 129(?):170313. doi: 10.1016/j.peptides.2020.170313. [PMID: 32298774]
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  • Xiaoran Zhu, Yaomeng Huang, Shuyu Li, Ning Ge, Tongxin Li, Yu Wang, Kunshen Liu, Chao Liu. Glucocorticoids Reverse Diluted Hyponatremia Through Inhibiting Arginine Vasopressin Pathway in Heart Failure Rats. Journal of the American Heart Association. 2020 05; 9(10):e014950. doi: 10.1161/jaha.119.014950. [PMID: 32390535]
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