Mast cell degranulation in hemorrhagic shock in rats and the effects of vasoactive intestinal peptide, aprotinin and H1 and H2-receptor blockers on degranulation.

Abstract:

:Various stressful stimuli cause mast cell degranulation. Hemorrhagic shock is one such stressful stimulus which may cause mast cell degranulation and histamine release. Histamine may be involved in the pathophysiology of hemorrhage. It was reported that there are large amounts of histamine in the anterior and posterior lobes of the pituitary and the adjacent median eminence of the hypothalamus. Most of the histamine in the posterior pituitary is in mast cells. In addition, both vasoactive intestinal peptide (VIP) and histamine-containing neurons are available in the hypothalamus. It therefore seems reasonable to suppose that these three systems (i.e., mast cells, VIP-containing neurons, and histamine-containing neurons) may play an important role in the progression of hemorrhagic shock. 66 albino rats (200-250 g) of either sex were used. The presence of mast cells was examined by light microscopy. Hemorrhage caused mast cell degranulation in a correlation with the amount of blood loss. In all cases, the most intense degranulation was observed in the hypothalamus, especially the nucleus arcuatus, and in the subcutaneous tissue. The intensity of degranulation gradually decreased in the peripheral blood vessel, peritoneum and omentum, in this order. VIP prevented degranulation, but aprotinin and H1 and H2 receptor blockers did not.

journal_name

Pharmacology

journal_title

Pharmacology

authors

Tikiz H,Tunçel N,Gürer F,Baycu C

doi

10.1159/000138826

subject

Has Abstract

pub_date

1991-01-01 00:00:00

pages

47-52

issue

1

eissn

0031-7012

issn

1423-0313

journal_volume

43

pub_type

杂志文章
  • Protective effect of the serotonin receptor antagonist cinanserin in two canine models of pacing-induced myocardial ischemia.

    abstract::Previous studies have indicated that structurally dissimilar serotonin2 (5HT2) antagonists can protect globally ischemic/reperfused reperfused rat hearts. We therefore determined if the 5HT2 antagonist cinanserin can protect the ischemic myocardium in two models of pacing-induced ischemia in anesthetized dogs. In one ...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000139294

    authors: Grover GJ,Parham CS,Youssef S,Ogletree ML

    更新日期:1995-05-01 00:00:00

  • Cardiac gap junction channels are upregulated by metoprolol: an unexpected effect of beta-blockers.

    abstract:BACKGROUND/AIMS:Since beta-adrenoceptors have been shown to affect cardiac gap junction channels, we wanted to elucidate the possible effect of metoprolol on the gap junction protein connexin-43, using racemic RS-metoprolol or the isomer R-metoprolol (no beta-adrenoceptor blockade) or S-metoprolol (beta(1)-adrenoceptor...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000276982

    authors: Salameh A,Blanke K,Dhein S,Janousek J

    更新日期:2010-01-01 00:00:00

  • Is the growth of brown adipocytes necessary for cold acclimation in mice?

    abstract::Chronic exposure to cold increases the growth of brown adipose tissue and the resistance to more severe cold, thus improving thermogenesis. The present study examined the possibility that dietary compounds can modify cold acclimation. Adenosine (ADO) or adenine (ADE) were administered in drinking water (0.05%, w/v) fo...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000028315

    authors: Nishimura M,Moriya M,Saitoh M,Murakoshi N,Shimizu Y

    更新日期:1999-09-01 00:00:00

  • Antidiarrheal activity of wood creosote: inhibition of muscle contraction and enterotoxin-induced fluid secretion in rabbit small intestine.

    abstract::Wood creosote has long been used as an antidiarrheal agent, but its mechanism of action is not well understood. To elucidate the mechanism of its antidiarrheal activity, we have addressed questions whether it inhibits fluid secretion induced by Escherichia coli heat-stable enterotoxin (STa) in rabbit jejunum in vivo, ...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000056092

    authors: Ogata N,Shibata T

    更新日期:2001-01-01 00:00:00

  • Direct Interaction of Daxx and Androgen Receptor Is Required for Their Regulatory Activity in Cholesterol Biosynthesis.

    abstract:INTRODUCTION:Homeostasis of cholesterol is crucial for cellular function, and dysregulated cholesterol biosynthesis is a metabolic event that can lead to hepatic and cardiovascular abnormalities. OBJECTIVE:The aim of this study was to investigate the effects and mechanisms of domain-associated protein (Daxx) and andro...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000506488

    authors: Li TP,Sun SW,Xiong GZ,Qiu F,Yang DM,Sun SY,Xie XJ,Liao DF,Chen JX,Tuo QH

    更新日期:2020-07-21 00:00:00

  • Monophosphoryl lipid A preserves myocardial contractile function following multiple, brief periods of coronary occlusion in dogs.

    abstract::The effects of a 1- or 24-hour pretreatment regimen with monophosphoryl lipid A (MLA, 35 micrograms/kg i.v.) on myocardial stunning produced by repetitive coronary occlusions were studied in barbital-anesthetized dogs. Regional segment function (%SS) and myocardial blood flow were measured by sonomicrometry and the ra...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000139329

    authors: Yao Z,Elliott GT,Gross GJ

    更新日期:1995-09-01 00:00:00

  • Honokiol and magnolol selectively interact with GABAA receptor subtypes in vitro.

    abstract::Honokiol and magnolol have been identified as modulators of the GABAA receptors in vitro. Our previous study suggested a possible selectivity of honokiol and magnolol on GABAA receptor subtypes. This possibility was examined in the current study by 3H-muscimol and 3H-flunitrazepam binding assays on various rat brain m...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000056110

    authors: Ai J,Wang X,Nielsen M

    更新日期:2001-07-01 00:00:00

  • Adrenergic activity of ortho-, meta-, and para-octopamine.

    abstract::DL-o-, and p-octopamine were tested for beta- and alpha-adrenergic activity in rats. When compared to DL-isoproterenol, a beta-adrenergic agonist, all three isomers failed to show significant beta-adrenergic activity as assessed by intiation of thirst and by increase in tail skin temperature. All three isomers increas...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000137250

    authors: Fregly MJ,Kelleher DL,Williams CM

    更新日期:1979-01-01 00:00:00

  • Effect of vasoactive intestinal peptide and naloxone combination on urinary N-acetyl-beta-D-glucosaminidase level and kidney histology of rats exposed to severe hemorrhage.

    abstract::Renal hypoperfusion which occurs in hemorrhagic shock creates an environment in which cellular injury and organ dysfunction can occur during the episode of shock as well as reoxygenation and reperfusion. At the same time, mast cell degranulation which is observed during hemorrhage may have an additional deleterious ef...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000139097

    authors: Akin MZ,Tunçel N,Gürer F,Kural N,Uslu S

    更新日期:1993-09-01 00:00:00

  • Additional antilipoperoxidant activities of alpha-tocopherol and ascorbic acid on membrane-like systems are potentiated by rutin.

    abstract::The effects of alpha-tocopherol, ascorbic acid and rutin on peroxidative processes were studied in xanthine-xanthine oxidase system, linoleic acid ufasomes and human erythrocyte membranes. In these three systems, tested compounds scavenge superoxide anion radicals or inhibit lipid peroxidation in a concentration-depen...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000138807

    authors: Nègre-Salvayre A,Affany A,Hariton C,Salvayre R

    更新日期:1991-01-01 00:00:00

  • Tissue distribution of primaquine in the rat.

    abstract::The distribution of primaquine was measured in seven rat tissues at 15-180 min after the intraperitoneal injection of the antimalarial 8-aminoquinoline. The half-life of unmetabolized primaquine was 4.0 h in lung, 1.7-1.9 h in blood, spleen, kidney and heart, and 1.2 h in liver. At each interval, the concentrations of...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000137508

    authors: Holbrook DJ Jr,Griffin JB,Fowler L,Gibson BR

    更新日期:1981-01-01 00:00:00

  • Effect of (+)-cyanidanol-3 on the changes in liver glutathione content and lipoperoxidation induced by acute ethanol administration in the rat.

    abstract::Acute ethanol administration to rats fasted overnight resulted in a significant decrease in the content of glutathione (GSH) of the liver concomitantly with a partial increase in oxidized glutathione levels, representing a net 38% decrease in total GSH equivalents. In these conditions, liver lipoperoxidation is signif...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000137514

    authors: Videla LA,Fernández V,Valenzuela A,Ugarte G

    更新日期:1981-01-01 00:00:00

  • Evidence of nonlinear pharmacokinetics of methotrexate in the rat.

    abstract::Three doses (0.31, 3.1 and 31 mg/kg) of methotrexate (MTX) were given intravenously to rats. The resulting concentration-time curves in plasma (normalized by dividing the plasma concentration by a multiple of the dose) were not superimposable, indicating nonlinear plasma pharmacokinetics. In liver, kidney, bone marrow...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000137723

    authors: Scheufler E

    更新日期:1982-01-01 00:00:00

  • Effects of 2(3)-tert-butyl-4-hydroxyanisole pretreatment on cefpiramide binding to mouse glutathione S-transferases.

    abstract::Binding of cefpiramide (CPM) and other beta-lactam antimicrobial agents to 2(3)-tert-butyl-4-hydroxyanisole (BHA)-induced liver glutathione (GSH) S-transferases (EC 2.5.1.18) from CD-1 mice was studied. A marked induction of hepatic GSH S-transferase from mice fed BHA was observed. Gel chromatography of liver cytosol ...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000138600

    authors: Nishiya H,Haga T,Nozue N,Komatsu T,Baba M,Ueda Y,Ono Y,Kunii O

    更新日期:1989-01-01 00:00:00

  • Actions of mibefradil, efonidipine and nifedipine block of recombinant T- and L-type Ca channels with distinct inhibitory mechanisms.

    abstract::We compared detailed efficacy of efonidipine and nifedipine, dihydropyridine analogues, and mibefradil using recombinant T- and L-type Ca2+ channels expressed separately in mammalian cells. All these Ca2+ channel antagonists blocked T-type Ca2+ channel currents (I(Ca(T))) with distinct blocking manners: I(Ca(T)) was b...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000094900

    authors: Lee TS,Kaku T,Takebayashi S,Uchino T,Miyamoto S,Hadama T,Perez-Reyes E,Ono K

    更新日期:2006-01-01 00:00:00

  • Mechanism of the antihypertensive effect of FCE 22716, a new ergoline derivative, in the spontaneously hypertensive rat.

    abstract::Both acute and chronic oral administration (1-20 mg/kg) of FCE 22716, a new ergoline derivative, resulted in a dose-related fall of arterial blood pressure lasting for more than 6 h. Tachycardia was observed only at high dosages. Yohimbine, propranolol and indometacin did not modify its antihypertensive effect; on the...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000138523

    authors: Salvati P,Bondiolotti GP,Caccia C,Vaghi F,Bianchi G

    更新日期:1989-01-01 00:00:00

  • Histamine H(3) receptors are involved in the protective effect of ghrelin against HCl-induced gastric damage in rats.

    abstract::In the present study, the effects of ghrelin against the gastric damage induced by intragastric administration of 0.6 N HCl and the involvement of histamine H₃ receptors (H₃Rs) were investigated in conscious rats with selective H₃R ligands. Intraperitoneal (i.p.) injection of ghrelin (40 μg/kg) significantly reduced (...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000320110

    authors: Adami M,Pozzoli C,Leurs R,Stark H,Coruzzi G

    更新日期:2010-01-01 00:00:00

  • Effect of YM-44781, YM-44778 and YM-49598, novel tachykinin antagonists, in a drug-induced bladder contraction model.

    abstract::The radioligand binding profiles and in vivo pharmacological characteristics of YM-44781, YM-44778 and YM-49598, novel non-peptide tachykinin receptor antagonists, were examined and compared to those of FK-888 and GR-159897. Since no functional NK(3) receptors were found in the rat bladder, the emphasis will be on the...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000056193

    authors: Choppin A,Groke G,Bringas A,Stepan G,Dillon MP

    更新日期:2002-05-01 00:00:00

  • Metabolism of sennosides--an overview.

    abstract::The metabolism of sennosides is discussed in view of the results obtained during the last years. Rhein anthrone is to be considered as the ultimate active form produced by microorganisms in the colon. Several contributions of this senna symposium bring complementary information of utmost interest. ...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000138431

    authors: Lemli J

    更新日期:1988-01-01 00:00:00

  • Subcellular distribution of SERCA and calcium-activated ATPase in rabbit and human urinary bladder smooth muscle.

    abstract::Previous studies have demonstrated that calcium storage and release from IP3-dependent sites in the sarcoplasmic reticulum play an important role in the contractile response of the rabbit urinary bladder to both field stimulation (mediated via neurotransmitter release) and bethanechol (direct muscarinic stimulation). ...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000139543

    authors: Levin RM,Nicholas TJ,Snitkoff GG,Mandell J,Russell D,Wilbur HJ,Mogavero LJ

    更新日期:1997-12-01 00:00:00

  • Study of the vasodilating activity of salbutamol on dog coronary arteries. Unexpected effects of methylene blue.

    abstract::The vascular relaxant effect of salbutamol and its dependence on the endothelium were studied in the isolated dog coronary artery, precontracted with prostaglandin F2 alpha. Salbutamol induced a concentration-dependent relaxation which was partially inhibited by removal of endothelial cells. Atenolol 10(-6) mol/l, a b...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000138804

    authors: Bernard F,Jouquey S,Hamon G

    更新日期:1991-01-01 00:00:00

  • Pitavastatin inhibits upregulation of intermediate conductance calcium-activated potassium channels and coronary arteriolar remodeling induced by long-term blockade of nitric oxide synthesis.

    abstract:UNLABELLED:We have reported that intermediate conductance Ca(2+)-activated K(+) channels (ImK) showed augmented expression in angiotensin II (AII) type 1 receptor-dependent manner in post-ischemic rat heart. ImK has tyrosine phosphorylation sequence in the C-terminus and motifs for NFkappaB and AP1 in the promoter. Whi...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000070455

    authors: Terata Y,Saito T,Fujiwara Y,Hasegawa H,Miura H,Watanabe H,Chiba Y,Kibira S,Miura M

    更新日期:2003-08-01 00:00:00

  • Effects of acetaldehyde on action potentials and Ca2+ currents in single atrial myocytes from the bullfrog.

    abstract:AIM:The purpose of the present study was to examine the effects of acetaldehyde on the contractile force and membrane potentials and currents in the bullfrog heart. METHODS:Contractile force was recorded using right atrial tissues, and membrane potentials and currents were measured by using whole cell patch clamp meth...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000342388

    authors: Chen FS,Satoh Y,Ide Y,Sugano T,Iimura M,Momose Y,Tsuchida K,Tagami M

    更新日期:2012-01-01 00:00:00

  • Involvement of the nitric oxide/cyclic guanylate monophosphate pathway in the pilocarpine-induced seizure model in mice.

    abstract::The present study was designed to investigate the involvement of the nitric oxide (NO)/cyclic guanylate monophosphate pathway in pilocarpine-induced seizures in mice. Male Swiss mice (26-32 g) were used as the in vivo model. The following pharmacological tools were utilized: the non-selective NO synthase (NOS) inhibit...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000346268

    authors: Vasconcelos Rios ER,Moura Rocha NF,Rodrigues Carvalho AM,Freire Vasconcelos L,Leite Dias M,de Carvalho Lima CN,Soares Lopes K,Cavalcante Melo FH,de França Fonteles MM

    更新日期:2013-01-01 00:00:00

  • Alterations in myocardial adenylate cyclase in spontaneously hypertensive rats.

    abstract::Particulate fractions of myocardium taken from spontaneously hypertensive rats (SHR) contained an adenylate cyclase system that was less responsive than normotensive Wistar Kyoto rats to norepinephrine, isoproterenol (mixed beta-agonist), salbutamol (beta 2-agonist), dobutamine (beta 1-agonist), dopamine, histamine, a...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000137303

    authors: Palmer GC,Greenberg S

    更新日期:1979-01-01 00:00:00

  • Effect of repeated administration of U-50,488H, a kappa opioid receptor agonist, on central 5-HT1 and 5-HT2 receptors in the rat.

    abstract::The effect of repeated administration of U-50,488H, a kappa-opioid receptor agonist, on the development of tolerance to its analgesic effect and on the 5-HT1 and 5-HT2 receptors in the cerebral cortex and spinal cord of the rat were determined. Male Sprague-Dawley rats were injected twice daily with U-50,488H, (25 mg/...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000138591

    authors: Gulati A,Ramarao P,Bhargava HN

    更新日期:1989-01-01 00:00:00

  • Lack of effect of intravenous hypertonic glucose on the intensity of alcohol intoxication induced experimentally and observed in patients of an emergency room.

    abstract::In the present paper, two experiments are performed to test the efficacy of the intravenous administration of hypertonic glucose (25 or 50%) in alcoholic intoxication. In a first experiment, 10 healthy, nonstarved volunteers, received 15 min after the ingestion of 1.0 g/kg alcohol, 40 ml of 25% glucose i.v., the same ...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000137769

    authors: Masur J,de Souza ML,Laranjeira RR,Zwicker AP,Formigoni GG

    更新日期:1983-01-01 00:00:00

  • Prolonged analgesia induced by cathinone. The role of stress and opioid and nonopioid mechanisms.

    abstract::Cathinone, the active principle of Catha edulis (khat), shows long-lasting analgesic effects when the tail-flick test is used in rats. The involvement of monoamines, endogenous opioids and stress in this analgesic effect was tested. Both early (30 min) and late (24 h) analgesic effects of cathinone were prevented by r...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000138023

    authors: Nencini P,Ahmed AM,Anania MC,Moscucci M,Paroli E

    更新日期:1984-01-01 00:00:00

  • Hepatic cytochrome P-450-dependent metabolism and enzymatic conjugation of foreign compounds in vitamin A-deficient rats.

    abstract::The temporal effects of vitamin A deficiency on hepatic cytochrome P-450-dependent and conjugation reactions were studied in the rat. Cytochrome P-450 levels and N-methyl-p-chloroaniline N-demethylase activity were significantly reduced in the deficient animals. No other changes in parameters dependent on cytochrome P...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000137457

    authors: Siddik ZH,Drew R,Litterst CL,Mimnaugh EG,Sikic BI,Gram TE

    更新日期:1980-01-01 00:00:00

  • Influence of tetanus and typhoid vaccines on hepatic drug metabolism.

    abstract::Several experiments suggested that vaccines might inhibit liver drug-metabolizing enzymes, an assumption in agreement with other findings obtained with most immuno-enhancing agents. A direct, non-specific activation of macrophages with subsequent release of interleukin 1 may account for this inhibition. The purpose of...

    journal_title:Pharmacology

    pub_type: 杂志文章

    doi:10.1159/000138370

    authors: Descotes J,Guillermin A,Evreux JC

    更新日期:1988-01-01 00:00:00