Results 161 to 170 of about 7,687 (206)

Histamine H₁-receptor-mediated modulation of NMDA receptors signaling responses. [PDF]

Pharmacol Res Perspect
Arrang JM, Armand V.
europepmc   +1 more source

Histamine-induced cytosolic calcium mobilization in human bronchial smooth muscle cells. [PDF]

J Smooth Muscle Res
Choi KJ, Jeon WY, Lee MY, Kim SH, Park HS.   +4 more
europepmc   +1 more source

The relationship between serum eosinophil peroxidase and major basic protein levels in relation to severity and response to H1 antihistamines in chronic spontaneous Urticaria. [PDF]

PLoS One
Nguyen CTK, Pham LT, Le MH, Le DH, Vu MN.   +4 more
europepmc   +1 more source

Neurotransmitters and Immunity: Molecular Mechanisms, Biological Functions, Diseases, and Potential Therapeutic Targets. [PDF]

MedComm (2020)
Li G, Li F, Tang Y, Guo S, Yao Y, Fang Y, Zhang B, Jiang Y, Wang J, Wu D, Cheng J, Huang Z, Xin Z, Zhang T.   +13 more
europepmc   +1 more source

Comparing the effectiveness of four antihistamines with olopatadine in healthy Thoroughbred horses.

J Vet Med Sci
Ikeda Y, Kuroda T, Mita H, Tamura N, Ohta M.   +4 more
europepmc   +1 more source

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Pharmacokinetic Optimisation of Histamine H1-Receptor Antagonist Therapy

Clinical Pharmacokinetics, 1991
Second-generation, relatively nonsedating histamine H1-receptor antagonists (H1-RA) are extensively used worldwide for the symptomatic treatment of allergic rhinoconjunctivitis and chronic urticaria. Information about the pharmacokinetics and pharmacodynamics of these medications, while still incomplete, is now sufficient to permit optimisation of ...
F. Estelle, R. Simons, Keith J. Simons
openaire   +2 more sources

Histamine H1-receptor antagonist activity assessed in conscious dogs

Journal of Pharmacological Methods, 1987
A simple, minimally invasive technique is described which allows assessment of histamine H1-receptor antagonist activity in conscious dogs. The technique is based on the inhibition of the tachycardia caused by intravenous administration of the H1-receptor agonist, 2-pyridylethylamine.
A, Wright, P, Raval, R J, Eden, D A, Owen   +3 more
openaire   +2 more sources