Диссертация (1174246), страница 24
Текст из файла (страница 24)
Res. Int. – 2014. – Vol. 2014. – ID 761264. – doi:10.1155/2014/761264.219. Panuganti, S. D. Enhanced xenobiotic-induced hepatotoxicity and Kupffercell activation by restraint-induced stress / S. D. Panuganti, F. D. Khan, C. K. Svensson// J. Pharmacol.
Exp. Ther. – 2006. – Vol. 318, Iss. 1. – P. 26–34.220. Physical and psychological stress in rats enhances colonic epithelial permeability via peripheral CRH / P. R. Saunders[et al.] // Dig. Dis. Sci. – 2002. – Vol. 47,Iss. 1. – P. 208–215.221. Psychosocial stress and liver disease status / C. C.
Vere [et al.] // World JGastroenterol. – 2009. – Vol. 15, Iss. 24. – P. 2980-2986.222. Psychosocial stress, personality and the severity of chronic hepatitis C /J. Nagano [et al.] // Psychosomatics. – 2004. – Vol. 45, Iss. 2. – P. 100–106.223. Powers, S. K. Exercise-Induced Oxidative Stress: Cellular Mechanisms andImpact on Muscle Force Production / S. K. Powers, M. J. Jackson // Physiol. Rev. –2008.
– Vol. 88, Iss. 4. – Р. 1243–1276.224. Rapid induction of neurotrophin mRNAs in rat glial cell cultures by Semax, an adrenocorticotropic hormone analog / M. I. Shadrina [et al.] // Neurosci. Lett. –2001. – Vol. 308, Iss. 2. – P. 115–118.225. Redox Control of Antioxidant and Antihepatotoxic Activities of Cassia surattensis Seed Extract against Paracetamol Intoxication in Mice: In Vitro and In Vivo155Studies of Herbal Green Antioxidant / U. S. Uthaya Kumar [et al.] // Oxid. Med. CellLongev.
– 2016. – Vol. 2016. – ID 6841348. – doi: 10.1155/2016/6841348.226. Reduced expression of the melanocortin-1 receptor in human liver duringbrain death / S. Gatti [et al.] // Neuroimmunomodulation. – 2006. – Vol. 13, Iss. 1. –Р. 51–55.227. Regulation of Cu/Zn-superoxide dismutase expression via the phosphatidylinositol 3 kinase/Akt pathway and nuclear factor-κB / A. I. Rojo [et al.] // J. Neurosci. – 2004.
– Vol. 24, Iss. 33. – P. 7324–7334.228. Response of liver antioxidant defense system to acute and chronic physicaland psychological stresses in male rats / M. Jafari [et al.] // EXCLI J. – 2014. – Vol. 13.– P. 161–171.229. Rodrigues, A. R. Intracellular signaling mechanisms of the melanocortinreceptors: current state of the art / A. R. Rodrigues, H.
Almeida, A. M. Gouveia // Cell.Mol. Life Sci. – 2015. – Vol. 72, Iss. 7. – P. 1331–1345.230. Role of corticosterone in TNF and IL-6 production in isolated perfused ratliver / J. Liao [et al.] // Am. J. Physiol. – 1995. – Vol. 268, Iss. 3. – P. 699–706.231.Role of oxidative stress and molecular changes in liver fibrosis: a review /V.
Sánchez-Valle [et al.] // Curr. Med. Chem. – 2012. – Vol. 19, Iss. 28. –P. 4850–4860.232. Role of the Kupffer cell in mediating hepatic toxicity and carcinogenesis /R. A. Roberts [et al.] // Toxicol. Sci. – 2007. – Vol. 96, Iss. 1. – P. 2–15.233. Sadri, A.-R. Advances in Liver Regeneration: Revisiting HepaticStem/Progenitor Cells and Their Origin / A.-R. Sadri, M. G. Jeschke, A.-N. Saeid //Stem Cells Int. – 2016.
– Vol. 2016. – Article ID 7920897, 9 pages. – doi:10.1155/2016/7920897.234. Sahin, E., Gümüşlü S. Stress -dependent induction of protein oxidation, lipid peroxidation and antioxidants in peripheral tissues of rats: comparison of threestress models (immobilization, cold and immobilization-cold) / E.
Sahin, S. Gümüşlü //Clin. Exp. Pharmacol. Physiol. – 2007. – Vol. 34, Iss. 5–6. – P. 425–431.156235. Salas, M. Liver ultrastructure during acute stress / M. Salas, B. Tuchweber,P. Kourounakis // Pathol Res Pract. – 1980. – Vol. 167, Iss. 2–4. – P. 217-233.236. Sapolsky, R. The neuroendocrinology of stress and aging: the glucocorticoid cascade hypothesis / R. Sapolsky, L. Krey, B.
S. McEwen // Endocr. Rev. – 1986.– Vol. 7, Iss. 3. – P. 284–301.237. Selye, H. Stress in Health and Disease / H. Selye. – Boston : Butterrworths-Heinemann, 2013. – 1300 p.238. Semax, an ACTH(4-10) Analogue with Nootropic Properties, ActivatesDopamine- and Serotonergic Brain Systems in Animals / K. O. Eremin [et al.] // Neurochem. Res. – 2005. – Vol. 30, Iss. 12. – P.
1493–1500.239. Semax, an analog of ACTH(4-10) with cognitive effects, regulates BDNFand trkB expression in the rat hippocampus / O. V. Dolotov [et al.] // Brain. Res. –2006. – Vol. 1117, Iss. 1. – P. 54-60.240. Sharma, R. K. Morphological and morphometric studies on Liver in ratssubjected to repetetive heat stress / R. K. Sharma // Indian J. Med. Res. – 1997. –Vol. 106.
– P. 20–26.241. Shipston, M. J. Mechanism(s) of early glucocorticoid inhibition of ACTHsecretion from anterior pituitary corticotropes / M. J. Shipston // Trends Endocrinol.Metab. – 1995. – Vol. 6, Iss. 8. – P. 261–266.242. Singer, A. J. The temporal profile of increased transaminase levels in patients with acetaminophen-induced liver dysfunction / A.
J. Singer, T. R. Carracio,H. C. Mofenson // Ann. Emerg. Med. – 1995. – Vol. 26, Iss. 1. – P. 49–53.243. Skaper, S. D. The neurotrophin family of neurotrophic factors: an overview// Methods Mol. Biol. – 2012. – Vol. 846. – P. 1–12.244. Sterling, P. Allostasis: a new paradigm to explain arousal pathology / P.Sterling, J. Eyer // Handbook of Life Stress, Cognition and Health / ed.: S. Fisher,J. Reason. – New York : Wiley, 1988. – P. 629–649.245. Stratakis, C.
A. Neuroendocrinology and pathophysiology of the stress system / C. A. Stratakis, G. P. Chrousos // Ann. NY Acad. Sci. – 1995. – Vol. 771. –P. 1–18.157246. Superoxide anions and hydrogen peroxide induce hepatocyte death by different mechanisms: Involvement of JNK and ERK MAP kinases / L. Conde de la Rosa[et al.] // J.
Hepatology. – 2006. – Vol. 44, Iss. 5. – Р. 918–929.247. Sympathoadrenal system in stress. Interaction with the hypothalamicpituitaryadrenocortical system / R. Kvetnansky [et al.] // Ann. NY Acad. Sci. – 1995. –Vol. 771. – P. 131–158.248. Swain, M. G. I. Stress and hepatic inflammation / M. G. Swain // Am.
J.Physiol. Gastrointest. Liver Physiol. – 2000. – Vol. 279, Iss. 6. – P. 1135-1138.249. Synthetic ACTH analogue semax displays nootropic-like activity in human/ A. Ya Kaplan [et al.] // Neuroscie. Res. Comm. – 1996. – Vol. 19, Iss.2. –P. 115–123.250. Targeting melanocortin receptors as a novel strategy to control inflammation / A. Catania [et al.] // Pharmacol. Rev.
– 2004. – Vol. 56, Iss. 1. – P. 1–29.251. The Effect of Semax and Its C-End Peptide PGP on the Morphology andProliferative Activity of Rat Brain Cells During Experimental Ischemia: A Pilot Study /V. V. Stavchansky [et al.] // J. Mol. Neurosci. – 2011. – Vol. 45, Iss.
2. – P. 177–185.252. The inhibition of lipid autoxidation by human serum and its relation to serum proteins and alpha-tocopherol / J. Stocks [et al.] // Clin. Sci. Mol. Med. – 1974. –Vol. 47, Iss. 3. – P. 223–233.253. The lighter side of BDNF / E.
E. Noble [et al.] // Am. J. Physiol. Regul. Integr. Comp. Physiol. – 2011. – Vol. 300, Iss. 5. – P. R1053–R1069.254. The Liver: Biology and Pathobiology / I. M. Arias [et al.]. – 5th ed. –Wiley, 2009. – 1216 p.255. The melanocortin system in control of inflammation / A. Catania [et al.] //Scientific World Journal. – 2010. – Vol. 10. – P.
1840–1853. – URL:http://dx.doi.org/10.1100/tsw.2010.173.256. The peptide semax affects the expression of genes related to the immuneand vascular systems in rat brain focal ischemia: genome-wide transcriptional analysis /E. V. Medvedeva [et al.] // BMC Genomics. – 2014. – N 15. – P. 228.
– doi:10.1186/1471-2164-15-228.158257. The restraint stress-induced elevation in plasma interleukin-6 negativelyregulates the plasma TNF-alpha level / H. Nukina [et al.] // Neuroimmunomodulation. –1998. – Vol. 5, Iss. 6. – P. 323–327.258. The Role of Alpha-1 and Alpha-2 adrenoceptors in restraint stress-inducedliver Injury in Mice / Q. Zhu [et al.] // PLoS ONE.
– 2014. – Vol. 9, Iss. 3. – e92125.259. Upregulation of hepatic melanocortin 4 receptor during rat liver regeneration / M. Xu [et al.] // J. Surg. Res. – 2016. – Vol. 203, Iss. 1. – P. 222–230.260. Wang, S. W. Effects of restraint stress and serotonin on macronutrient selection: a rat model of stress-induced anorexia // Eat. Weight.
Disord. – 2002. – Vol. 7,Iss. 1. – P. 23–31.261. Wang, X. Malondialdehyde regulates glucose-stimulated insulin secretionin murine islets via TCF7L2-dependent Wnt signaling pathway / X. Wang, X.G. Lei,J. Wang // Mol. Cell. Endocrinol. – 2014. – Vol.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
