Affiliations 

  • 1 Department of Physiology, School of Medical Sciences, Universiti Sains Malaysia Health Campus, 16150 Kubang Kerian, Malaysia
  • 2 Department of Physiology, School of Medical Sciences, Universiti Sains Malaysia Health Campus, 16150 Kubang Kerian, Malaysia. Electronic address: rahimah@kck.usm.my
  • 3 Department of Psychiatry, School of Medical Sciences, Universiti Sains Malaysia Health Campus, 16150 Kubang Kerian, Malaysia
  • 4 Department of Anatomy, School of Medical Sciences, Universiti Sains Malaysia Health Campus, 16150 Kubang Kerian, Malaysia
  • 5 Department of Neuroscience, School of Medical Sciences, Universiti Sains Malaysia Health Campus, 16150 Kubang Kerian, Malaysia
Acta Histochem, 2014 Jan;116(1):79-88.
PMID: 23810156 DOI: 10.1016/j.acthis.2013.05.004

Abstract

Recently, our research team has reported that Tualang honey was able to improve immediate memory in postmenopausal women comparable with that of estrogen progestin therapy. Therefore the aim of the present study was to examine the effects of Tualang honey supplement on hippocampal morphology and memory performance in ovariectomized (OVX) rats exposed to social instability stress. Female Sprague-Dawley rats were divided into six groups: (i) sham-operated controls, (ii) stressed sham-operated controls, (iii) OVX rats, (iv) stressed OVX rats, (v) stressed OVX rats treated with 17β-estradiol (E2), and (vi) stressed OVX rats treated with Tualang honey. These rats were subjected to social instability stress procedure followed by novel object recognition (NOR) test. Right brain hemispheres were subjected to Nissl staining. The number and arrangement of pyramidal neurons in regions of CA1, CA2, CA3 and the dentate gyrus (DG) were recorded. Two-way ANOVA analyses showed significant interactions between stress and OVX in both STM and LTM test as well as number of Nissl-positive cells in all hippocampal regions. Both E2 and Tualang honey treatments improved both short-term and long-term memory and enhanced the neuronal proliferation of hippocampal CA2, CA3 and DG regions compared to that of untreated stressed OVX rats.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.