Antihistaminic activity of Ethanolic extract of Capparis moonii W. fruit.

Author(s):  
Priya Gupta ◽  
Vanita Kanase

The purpose of the present work were intended to determine the antihistaminic activity of ethanolic extract of Capparis moonii W. fruits (EECM). Capparis moonii W. had been historically used in the diagnosis of cough and asthma and so we undertook this study to validate scientifically using appropriate animal models. Antihistamine is considered to be helpful for the treatment of allergic, thus, the antihistamine activity of an ethanolic extract of Capparis moonii W. in the current work was evaluated. To determine the doses, acute oral toxicity tests were conducted. Clonidine and haloperidol that induced cataleptic effect in Swiss albino mice were evaluated for antihistaminic activity at the different doses of 50mg/kg, 100mg/kg and 200mg/kg, p.o. and the evaluation is also done on guinea pig ileum tissue. The ethanolic extract of Capparis moonii W. fruits (50, 100, 200mg/kg, p.o.) and chlorpheniramine maleate (i.p.,10mg/kg) significantly inhibited (****P<0.0001) clonidine induced catalepsy but the extract donot inhibit haloperidol-induced catalepsy and histamine-induced contraction in guinea pig ileum tissue preparation shows that ethanolic extract of Capparis moonii W. inhibited the contractile activity of histamine. The result of our work shows that the ethanolic extract possesses antihistaminic activity. It can be reported that flavonoid present in the extract may be important for an antihistaminic effect and therefore may have a role in the asthma treatment.

1969 ◽  
Vol 47 (9) ◽  
pp. 755-762 ◽  
Author(s):  
M. Lefcort ◽  
L. E. Francis ◽  
K. I. Melville

Extracts of rat tissues (ear and abdominal skin, heart, cerebrum, spleen, kidney, lung, liver, stomach, and jejunum) were tested for their ability to antagonize histamine on the guinea pig ileum preparation. Antihistamine activity varied considerably between tissues; it was found to be highest in the ear skin and lowest in the jejunum and stomach. After pretreatment with semicarbazide (plus a pyridoxine-free diet) or reserpine, or after adrenalectomy, the antihistamine activity was reduced in some tissues but was increased in others. The variation in the behavior of the different tissues with these treatments made it impossible to interpret the distribution of antihistamine activity in terms of known sites of amine formation. After treatment with compound 48/80, however, there was an apparent parallelism between loss of antihistamine activity and depletion of mast cell histamine.


1990 ◽  
Vol 10 (1) ◽  
pp. 113-119 ◽  
Author(s):  
L. F. Alguacil ◽  
M. P. Lopez-Ruiz ◽  
J. C. Prieto ◽  
C. Alamo ◽  
E. Cuenca

Neither acute nor prolonged exposure to morphine altered cAMP content or spontaneous movements of longitudinal muscle-myenteric plexus strips of the guinea-pig ileum. By contrast, exogenous acetylcholine or electrical stimulation of the strips elicited both a decrease of cAMP concentration and a twitch response. Atropine blocked the effects of stimulation on these parameters. Addition of morphine to electrically stimulated strips inhibited the twitch response but did not affect cAMP levels. Incubation with morphine led to the development of tolerance to the inhibitory effect on twitch activity and prevented the fall in cAMP normally elicited by electrical stimulation. These results suggest that muscarinic activation is associated with a reduction of cAMP content, an effect which would be impaired in opiate-tolerant tissues.


2020 ◽  
Vol 11 ◽  
Author(s):  
Joedna Cavalcante Pereira ◽  
Indyra Alencar Duarte Figueiredo ◽  
Filipe Rodolfo Moreira Borges de Oliveira ◽  
Sarah Rebeca Dantas Ferreira ◽  
Giulyane Targino Aires Moreno ◽  
...  

Oceanapia magna Santos-Neto, Nascimento, Cavalcanti and Pinheiro sponges are distributed across tropical worldwide seas. Some studies of marine products have shown interesting activities in smooth muscle models. Hence, we assessed the effect of the ethanolic extract of Oceanapia magna. (OC-EtOH) on acute toxicity and gastrointestinal motility (in vitro and in vivo) in rodent models. On guinea pig ileum, OC-EtOH induced a concentration dependent contraction on basal tonus, which was not inhibited by atropine, but in the presence of pyrilamine or verapamil, the effect was antagonized. Contrastingly, on KCl- or histamine-induced contractions, OC-EtOH presented a transient contraction followed by a concentration-dependent relaxation. Moreover, OC-EtOH presented a relaxant profile on cumulative curves to CaCl2 and tonic contraction induced by S-(-)-BayK8644, through Cav blockade. The acute toxicity assay showed that OC-EtOH (2,000 mg/kg, p.o.) did not present any sign of toxicity in female mice. Additionally, OC-EtOH presented antidiarrheal effect in mice, increased the intestinal normal transit and reduced the castor oil-induced intestinal transit. Thus, OC-EtOH presented a dual effect on guinea pig ileum promoting contraction through activation of H1 and CaV, and relaxation through CaV blockade, besides the effect on upper gastrointestinal transit in mice, showing a potential medicinal use of this sponge in intestinal diseases such as diarrhea.


1992 ◽  
Vol 26 ◽  
pp. 321
Author(s):  
Corrado Blandizzi ◽  
Gianfranco Natale ◽  
Mario Del Tacca

2012 ◽  
Vol 10 (4) ◽  
pp. 49-53
Author(s):  
Kirill Leonidovich Kryshen ◽  
Dmitriy Valentinovich Demchenko ◽  
Olga Nikolayevna Pozharitskaya ◽  
Marina Nikolayevna Makarova ◽  
Yaroslav Aleksandrovich Gushchin ◽  
...  

The effect of the peptide substance on the induced production of histamine by culture of basophile, interaction of the preparation with the H1-histamine receptors and possible sedative effect on animal models were studied. The introduction of the peptide substance in cell culture of basophile didn’t have a significant effect on the histamine release. Study of the interaction of the polypeptide substance with H1-histamine receptors of guinea pig ileum showed that the preparation inhibits the response of unstriated muscles to histamine. The effect was similar to antihistamine drug - ketotifen. In the models of “open field” and “elevated criss-cross labyrinth” it was found that the peptide preparation hasn’t a sedative effect.


2019 ◽  
Vol 5 (1) ◽  
pp. 13
Author(s):  
Cholis Abrori ◽  
Khana Nurfadhila ◽  
Elly Nurus Sakinah

Basil leaves are widely used as herbal remedies and have proven many benefits because the content of phytonutrients includes antioxidants, but at certain doses a compound retains a probability of causing toxicity in the body. This study aims to determine the acute toxicity of ethanolic extract of basil leaves seen from the value of LD50 range and renal histopathology which is the vital organ of the target of toxicity in the body. The method of acute oral toxicity test was OECD 420 fix dose procedure method with a group of 5 Balb/c female mice given a multilevel dosage. The initial dose is 2000 mg/Kg.b.w selected on a sighting study as a dose that may cause mild toxicity symptoms but does not cause death. There are 2 groups consist of treatment with dose at LD50 value and control. The result of this research showed that LD50 value of ethanol extract of Ocimum sanctum > 2000 mg/Kg.b.w. The mean renal histopathologyc scores between the control and the treatment were significantly different by The Mann-Whitney test with significance value of p=0.018. Ocimum sanctum ethanolic extract is classified as non-toxic compounds but there was a change in renal histopathology of mice in the form of focal lesions after acute exposure at highest dose of OECD 420 method. Keywords: acute toxicity test, renal histopathology, basil leaves


1977 ◽  
Vol 29 (1) ◽  
pp. 57-58 ◽  
Author(s):  
T. Segawa ◽  
M. Hosokawa ◽  
K. Kitagawa ◽  
H. Yajima

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