LEGUMINOSAE (FABACEAE ) - PAPILIONOIDEAE Arachis hypogaea  L.

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 Thai / English name

  • ถั่วลิสง*

[1-1] of 1 article(s) found

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[1] DICLOFENAC ENHANCES ALLERGIC RESPONSES IN A MOUSE PEANUT ALLERGY MODEL.
BOL-SCHOENMAKERS,M.;BLEUMINK,R.;REZENDE,M.MARCONDES;ET AL.
CLIN EXP ALLERGY 2011 Vol.41(3),424-33  $62172 [Full]

Part Used : เมล็ด
Activity : DRUG INTERACTION
Solvent/Active Compound : Peanut extract
Type of experiment : in vivo
Type of animal : mouse
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Intraperitoneal
Dose/Conc.(herb) : 6 mg peanut extract + 15 microgram cholera toxin for 3 consecutive days/week
Duration : 3 weeks
Type of interaction : Pharmacokinetics
Interaction with drug : Diclofenac
Dose/Conc.(drug) : 1 mg/kg
Result : Positive
Remark : Administration of diclofenac before peanut extract (PE) + cholera toxin (CT) expsosure resulted in significant increases of serum levels of PE-specific lgG1 and lgE. Furthermore, mMCP-1, a measure for mast cell degranulation in vivo, was enhanced by diclofenac upon an oral chanllenge with PE. When mice were treated with 0 or 25 mg/kg diclofenac and PE in the absence of CT, no PE- specific antibodied could be detected, indicating that diclofenac at this dose is not able to elicit an allergic response in the absence of the adjuvant CT.

Part Used : เมล็ด
Activity : DRUG INTERACTION
Solvent/Active Compound : Peanut extract
Type of experiment : in vivo
Type of animal : mouse
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Intraperitoneal
Dose/Conc.(herb) : 6 mg peanut extract + 15 microgram cholera toxin for 3 consecutive days/week
Duration : 3 weeks
Type of interaction : Pharmacokinetics
Interaction with drug : Diclofenac
Dose/Conc.(drug) : 10 mg/kg
Result : Positive
Remark : Administration of diclofenac before peanut extract (PE) + cholera toxin (CT) expsosure resulted in significant increases of serum levels of PE-specific lgG1 and lgE. Furthermore, mMCP-1, a measure for mast cell degranulation in vivo, was enhanced by diclofenac upon an oral chanllenge with PE. When mice were treated with 0 or 25 mg/kg diclofenac and PE in the absence of CT, no PE- specific antibodied could be detected, indicating that diclofenac at this dose is not able to elicit an allergic response in the absence of the adjuvant CT.

Part Used : เมล็ด
Activity : DRUG INTERACTION
Solvent/Active Compound : Peanut extract
Type of experiment : in vivo
Type of animal : mouse
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Intraperitoneal
Dose/Conc.(herb) : 6 mg peanut extract + 15 microgram cholera toxin for 3 consecutive days/week
Duration : 3 weeks
Type of interaction : Pharmacokinetics
Interaction with drug : Diclofenac
Dose/Conc.(drug) : 25 mg/kg
Result : Positive
Remark : Administration of diclofenac before peanut extract (PE) + cholera toxin (CT) expsosure resulted in significant increases of serum levels of PE-specific lgG1 and lgE. Furthermore, mMCP-1, a measure for mast cell degranulation in vivo, was enhanced by diclofenac upon an oral chanllenge with PE. When mice were treated with 0 or 25 mg/kg diclofenac and PE in the absence of CT, no PE- specific antibodied could be detected, indicating that diclofenac at this dose is not able to elicit an allergic response in the absence of the adjuvant CT.

Part Used : เมล็ด
Activity : DRUG INTERACTION
Solvent/Active Compound : Peanut extract
Type of experiment : in vivo
Type of animal : mouse
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Intraperitoneal
Dose/Conc.(herb) : 6 mg peanut extract for 3 consecutive/week
Duration : 3 weeks
Type of interaction : Pharmacokinetics
Interaction with drug : Diclofenac
Dose/Conc.(drug) : 1 mg/kg
Result : Negative
Remark : Administration of diclofenac before peanut extract (PE) + cholera toxin (CT) expsosure resulted in significant increases of serum levels of PE-specific lgG1 and lgE. Furthermore, mMCP-1, a measure for mast cell degranulation in vivo, was enhanced by diclofenac upon an oral chanllenge with PE. When mice were treated with 0 or 25 mg/kg diclofenac and PE in the absence of CT, no PE- specific antibodied could be detected, indicating that diclofenac at this dose is not able to elicit an allergic response in the absence of the adjuvant CT.

Part Used : เมล็ด
Activity : DRUG INTERACTION
Solvent/Active Compound : Peanut extract
Type of experiment : in vivo
Type of animal : mouse
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Intraperitoneal
Dose/Conc.(herb) : 6 mg peanut extract for 3 consecutive/week
Duration : 3 weeks
Type of interaction : Pharmacokinetics
Interaction with drug : Diclofenac
Dose/Conc.(drug) : 10 mg/kg
Result : Negative
Remark : Administration of diclofenac before peanut extract (PE) + cholera toxin (CT) expsosure resulted in significant increases of serum levels of PE-specific lgG1 and lgE. Furthermore, mMCP-1, a measure for mast cell degranulation in vivo, was enhanced by diclofenac upon an oral chanllenge with PE. When mice were treated with 0 or 25 mg/kg diclofenac and PE in the absence of CT, no PE- specific antibodied could be detected, indicating that diclofenac at this dose is not able to elicit an allergic response in the absence of the adjuvant CT.

Part Used : เมล็ด
Activity : DRUG INTERACTION
Solvent/Active Compound : Peanut extract
Type of experiment : in vivo
Type of animal : mouse
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Intraperitoneal
Dose/Conc.(herb) : 6 mg peanut extract for 3 consecutive days/week
Duration : 3 weeks
Type of interaction : Pharmacokinetics
Interaction with drug : Diclofenac
Dose/Conc.(drug) : 25 mg/kg
Result : Negative
Remark : Administration of diclofenac before peanut extract (PE) + cholera toxin (CT) expsosure resulted in significant increases of serum levels of PE-specific lgG1 and lgE. Furthermore, mMCP-1, a measure for mast cell degranulation in vivo, was enhanced by diclofenac upon an oral chanllenge with PE. When mice were treated with 0 or 25 mg/kg diclofenac and PE in the absence of CT, no PE- specific antibodied could be detected, indicating that diclofenac at this dose is not able to elicit an allergic response in the absence of the adjuvant CT.

Part Used : เมล็ด
Activity : DRUG INTERACTION
Solvent/Active Compound : Peanut extract
Type of experiment : in vivo
Type of animal : mouse
Type of study : -
N(Total) : -
N(Treatment) : -
Sex : -
Age : -
Route : Intraperitoneal
Dose/Conc.(herb) : 1 mg peanut extract
Duration : 3 days
Type of interaction : Pharmacokinetics
Interaction with drug : Diclofenac
Dose/Conc.(drug) : 1 mg/kg, 2 h before each oral PE exposure
Result : Positive
Remark : Administration of diclofenac before oral exposure to peanut extract (PE) did not abrogate oral tolerance induction, as PE-specific antibodies in serum were comparably low in diclofenac treated and vehicle-treated tolerized mice. In addition, cytokine levels in the supernatant of cultured splenocytes from PE-tolerized, diclofenac-treated mice were significantly lower compared with those in splenocyte cultures of non-tolerized mice. Noticeably, the ex vivo PE specific cytokine levels of diclofenac-treated tolerized mice were significantly higher compared with vehicle-treated tolerized mice, except in the case of lL-4.


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