By Armen A. Galoyan
From the reviews:
"Brain Neurosecretory Cytokines is a superb booklet, a veritable goldmine of knowledge, on the innovative of neuroscience. it may stimulate rules for destiny instructions in neuroscience for years yet to come. This quantity can be hugely beneficial for scientific libraries, neuroscientists, endocrinologists and graduate scholars in those fields." (Arthur S. Brecher, developments in Endocrinology & Metabolism, Vol. sixteen (6), 2005)
Read Online or Download Brain Neurosecretory Cytokines: Immune Response and Neuronal Survival PDF
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Extra resources for Brain Neurosecretory Cytokines: Immune Response and Neuronal Survival
500 III of each sample dilution was injected i/p into mice. Portions of suitable dilutions were also inoculated onto agar plates for precise enumeration of bacterial cells (colony-forming unit, CFU). Identification ofCFU of microorganisms was observed with different type-specific agglutination standard sera. Female pathogen-free BALB/c, C57BLl6J, C3H/HeJ, (CBAxC57BL/6J) F 1 strains of mice at the age of 6-8 weeks (Laboratory of Animals "Stolbovaya" of the RAMS, Moscow) were used in the experiments IIS-119.
White column, control without PRP-J. The black one, PRP-l treatment. - -- - -- - - ----- ----.. .... . - - - -_ - - - _ ... , 15 c 0 :w ~ C Ql o 10 c 0 u :I: C) 5 o A B c Figure 29. Dependence of GH production on the concentration of fibroblasts in culture under different PRP-I doses. Ordinate, GH concentrations (ug/ml) . 8,3 _10. 5 g/ml. 001). 001). Thus, the investigations carried out revealed the ability of PRP-1 to increase human GH production in transfected mouse fibroblast cultures. PRP-l increased the total and daily production of the hormone at the stage of monolayer formation, as well as at the stage of mature monolayer of fibroblasts.
Diluuon of GN, ~ -, OO~I IIIlI -50 ~1 • ·25~1 ~ . , Dill Figure 22. Effect ofNGN lysate on the expression ofTNF-a by LPS-stimulated macrophages . : ;; s. ~ IIIs Control with out ~ . 7 :'f) • 7 ~ -PRP. 7 ~I) Figure 23. Effect ofNGN and polypeptides on the secretion ofTNF-a by LPS-stimulated astrocytes. insignificant (Fig. 23-3, 6, 7). At the same time, PRP-1 doubled TNF-a secretion (Fig. 23-4). When PRP-1 and the NGH lysate were added simultaneously, the TNF-a activity increased almost 3 times (Fig.
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