[Effect of substance P on survival of rats after cerebral ischemia: the effect depends on behavior type]. / Vliianie substantsii P na vyzhivaemost' krys posle ishemii mozga: éffekt zavisit ot tipo o povedeniia.

In rats with different behaviour types in tests of "open field" and "forced swimming", influence of intraperitoneal administration of P-substance (PC) neuropeptide to survival and structural-metabolic changes in brain after double-sided ligating of carotid arteries. It was established that PC exerts different influence on stability to circulating cerebral hypoxia according to behaviour types: it increases stability in rats with passive behaviour type, decrease stability in rats with active behaviour type and does not influence on rats with middle behaviour type. Results shows the necessity of individual approach to peptide use with the view to increase stabilization to cerebral ischemia.

Delta sleep-inducing peptide as a factor increasing the content of substance P in the hypothalamus and the resistance of rats to emotional stress.

The influence of delta sleep-inducing peptide (DSIP, 60 and 120 nmole/kg, intraperitoneally) on the content of substance P (SP) in the hypothalamus of rats was studied in male rats of the August line. It was demonstrated that the administration of DSIP significantly increases the average content of SP in the hypothalamus, as well as its content in animals resistant to and predisposed to emotional stress. A daily one-time administration of DSIP before placing the rats in conditions of stress increases the content of SP in the hypothalamus which was decreased during emotional stress. The preliminary one-time administration of DSIP to animals subjected to a stressor influence also increases the SP content in the hypothalamus. It was established that a one-time administration of DSIP in a dose of 60 nmole/kg sharply decreases the classical manifestations of stress such as the hypertrophy of the adrenals and involution of the thymus.

[Effects of C-terminal fragment of substance P-CP 5-11 on the activity of neurons of the dorsal raphe nucleus]. / Vliianie C-kontsevogo fragmenta substantsii P-CP 5-11 na aktivnost' neironov dorsal'nogo iadra shva.

The experiments on Wistar rats showed that microinjection of C-terminal fragment of substance P-CP5-11 (1 microgram) into one of the antinociceptive system structure--dorsal raphe nucleus, caused a prolonged (24 hours of observation) analgetic effect by the hot plate test. Neuronal activity of dorsal raphe nucleus simultaneously enhanced. The CP5-11 antinociceptive activity was higher than the CP1-11 one. The conclusion is that CP1-11 and in particular its C-terminal fragment CP5-11 play a role in activation of antinociceptive system.

[Splenopentin--modulator of immunological and behavioral reactions in secondary immunodeficiency state induced by experimental alcoholism]. / Splenopentin--moduliator immunnykh i povedencheskikh reaktsii pri vtorichnom immunodefitsitnom sostoianii, vyzvannom éksperimental'nym alkogolizmom.

Effect of splenopentin on some patterns of immunity was studied in mice with chronic alcoholic intoxication. Splenopentin was administrated into animals once intraperitoneally (250 micrograms/kg). Administration of splenopentin was found to normalize several immunological patterns in animals with chronic alcoholic intoxication: the immune response to the thymus-dependent antigen sheep red blood cells and phagocytic activity of peritoneal macrophages. Also observations over C57B1/6 mice characterized by high level of alcoholic motivation showed that alcohol consumption in mice decreased after administration of splenopentin at a dose of 250 micrograms/kg during two weeks.

[Use of substance P fragments in experimental treatment of alcoholism]. / Primenenie fragmentov substantsii P dlia éksperimental'noi terapii alkogolizma.

Experiments on unbred male mice demonstrated qualitative differences in the pharmacological effect of substance P fragments (P1-4 and P5-11) injected intraperitoneally in a dose of 250 mcg/kg. Fragments P1-4 and P1-4 dodecylamide on the one hand, had a positive effect on the level of motivation which was displayed by lesser consumption of alcohol by the animals, and, on the other, possessed immunocorrective properties manifested by restoration of macrophage phagocytic activity and immune response to sheep erythrocytes, which were impaired by chronic alcoholic intoxication. Fragment P5-11 had no effect on alcoholic motivation and produced a directly contrary action on the immune system, it inhibited the formation of antibody-forming cells.

[Effects of SP1-11 and its N-terminal fragment SP1-4 on several indices of the microcirculatory system in stress]. / Izuchenie deistviia SP1-11 i ego N-kontsevogo fragmenta SP1-4 na nekotorye pokazateli sistemi mikrotsirkuliatsii pri stresse.

In the experiments on rats it was shown that 5-hour immobilization induced the disturbances of terminal blood flow, degranulation of mast cells, increase of venular permeability and contractile activity of lymphaticus. I/p injection SP1-11 (125 micrograms/kg) before stress aggravated the disturbances caused by immobilization. The prophylactic i/p injection SP1-4 induced tranquilizing (100%), sedative (30%) or narcosis (20%) effect. In the rats with sedative or narcosis effects the relative normalization of components of microcirculatory system was observed.

[Effects of substance P and its fragments in physiological and pathological pain]. / Vliianie substantsii P i ee fragmentov na fiziologicheskuiu i patologicheskuiu bol'.

It has been shown that substance P and its fragments can produce under certain conditions an analgetic effect on both physiological and pathological pain (i.e. on pain syndrome of spinal origin). The data obtained give evidence that prolonged hypoalgesia is caused by the injection of substance P and its fragments to nucleus raphe dorsal--a structure of the antinociceptive system. This analgetic effect can be initiated by the activation of the antinociceptive system influenced by substance P and or its fragments.

[Effect of fusaric acid on phosphoinositide metabolism in the erythrocyte membranes of rats with spontaneous hypertension]. / Vliianie fuzarovoi kisloty na metabolizm fosfoinozitidov membran éritrotsitov krys so spontannoi gipertoniei.

2- and 4-month-old male spontaneously hypertensive rats (SHR) were injected fusaric acid at a dose of 50 mg/kg body weight. Fusaric acid increased diphosphoinositide (DPI) and triphosphoinositide (TPI) levels in erythrocyte membranes of 4-month-old SHR by 41% and 20%, respectively. 32P incorporation into TPI decreased by 24% in 2- and by 20% in 4-month-old SHR. Phosphatidylinositol metabolism remained unchanged. The results also suggest that fusaric acid normalized DPI and TPI metabolism in erythrocyte membranes of SHR.

[Peptide therapy of sleep disorders in neurotic rats]. / Peptidnaia terapiia rasstroistv sna u nevrotizirovannykh krys.

As a result of chronic stress, anxiety appeared in the rats behaviour, motor activity increased, heart rate quickened, blood pressure raised, conditioned instrumental alimentary reflexes missed, the duration of deep phases of sleep lowered, time of falling asleep became longer, the number of awakening increased. The change in quantitative characteristics of sleep was accompanied by its worsening, especially of rapid sleep. Administration of substance P (SP) eledoisin hexopeptide (EH) (250 mcg/kg), 100-200 mcg/kg of delta sleep peptide and 10 mcg/kg of ethylcrotyl barbiturate improved the rats behaviour and sleep parameters. Calipnon accelerated falling asleep. Delta sleep peptide increased sleep duration. SP and EH restored not only the quantitative characteristics of deep phases of sleep but greatly improved their quality: lowered the blood pressure disrupted tachycardia, normalized the conditioned activity.

[Hemodynamic characteristics of polypeptide substance P compared to bradykinin and prostaglandin E1]. / Gemodinamicheskaia kharakteristika polipeptidnoi substantsii P v sravnenii s bradikininom i prostaglandinom E1.

The effective doses of substance P, bradykinin and prostaglandin E1 that induced depressor responses in rats and rabbits were compared. On molar conversion substance P showed the most pronounced activity. There was an essential difference in doses that evoked standard responses in rabbits (the preparations were administered into the right or left heart ventricle). For bradykinin the dose difference was fivefold and prostaglandin E1 twenty-twofold. Substance P did not undergo inactivation in the lungs.