Anticonvulsant and Precognitive Properties Of Novel Histamine H3 Receptor Antagonists in Male Adult Rats

الموضوعات

طب

الملخص

To determine the potential of histamine H3 receptor (H3R) ligands as new antiepileptic and precognitive drugs, aromatic ether derivatives ( 1-12 ) belonging to the no imidazole class of ligands, with high in-vitro binding affinity at human H3R, were tested for their in-vivo anticonvulsive activity in maximal electroshock (MES)-, Pentylenetetrazole (PTZ)-, and strychnine (STR)-induced seizure models in male adult rats having phenytoin (PHT) and valproic acid (VPA) as the reference antiepileptic drugs, pitolisant (PIT) as the standard H3R antagonist/inverse agonist, and donepezil (DOZ) as a reference precognitive drug. Among the H3R ligands ( 1- 12 ) tested in the current project, H3R antagonist 4 showed significant and dose dependent reduction in the duration of tonic hind limb extension (THLE) subsequent to acute systemic administration (5, 10, and 15 mg/kg, i.p.). Importantly, the protective action observed for H3R antagonist 4 in MES-induced seizure was comparable to that of the reference antiepileptic drug phenytoin (PHT), and was also reversed when rats were pretreated with the CNS penetrant pyrilamine (PYR) (10 mg/kg, i.p.), or with the selective H3R agonist R -(a)-methyl histamine (RAMH) (10 mg/kg, i.p.). Furthermore, the precognitive studies indicate that acute pre-training systemic administration of H3R antagonist 4 (2.5 mg/kg, i.p.) facilitated acquisition, whereas pre-testing acute administration of 4 (5 and 10 mg/kg, i.p.) improved retrieval. Interestingly, the precognitive effect of 4 on retrieval was completely abrogated when rats were pretreated with the centrally-acting H2R antagonist zolantidine (ZOL) but not the centrally acting H1R antagonist PYR, indicating that histaminergic pathways through activation of H2Rs appear to be participating in neuronal circuits involved in the retrieval processes. Taken together, our results show that H3R antagonist 4 demonstrates anticonvulsant properties in the MES-induced seizure model and improves cognitive performance through actions on different memory stages. Therefore, H3Rs may have implications for the treatment of degenerative disorders associated with impaired memory function and may represent a novel therapeutic pharmacological target to tackle cognitive problems associated with the chronic use of antiepileptic drugs.

روابط وملفات

التعريف والنوع

رقم الوثيقة

08e4a1c6-27ba-4e40-bde9-e6c3d4fd916d

رقم العقد

0

نوع الوسائط

Crawler

نوع المحتوى

الرسائل العلمية

صيغة المصدر

رسائل ماجيستير

نوع الملف

pdf text

أسماء الملفات

8175_1.pdf

بيانات النشر

ترجمة العنوان

دراسة فعالية عدد من مثبطات مستقبلات الهستامين-3 المستخلفة حديثا على نماذج بحثية مختلفة للصرع وضعف الذاكرة في فصيلة معينة من القوارض

ألقاب المؤلفين

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اللغة

English

المصدر والدورية

اسم المصدر

Anticonvulsant and Precognitive Properties Of Novel Histamine H3 Receptor Antagonists in Male Adult Rats

المحتوى والصفحات

عدد الصفحات

0

إشراف وإعداد

الإشراف

باسم صديق

الإعداد

علي قاسم سعد

الاقتباسات الببليوغرافية