A comparative assessment of age‐related nicotinamide adenine dinucleotide phosphate‐diaphorase positivity in the spinal cord and medulla oblongata of pigeons, rats, and mice

Author:

Jia Yunge1ORCID,Li Yinhua2,Hou Wei3,Wei Zichun3,Zhang Tianyi3,Wang Xinghang3,Wang Jie4,Tan Huibing3

Affiliation:

1. Department of Pathology Heji Hospital Affiliated of Changzhi Medical College Changzhi Shanxi China

2. College of Physical Education and Sport Rehabilitation Jinzhou Medical University Jinzhou Liaoning China

3. Department of Anatomy Jinzhou Medical University Jinzhou Liaoning China

4. Department of General Surgery Changzhi People's Hospital Affiliated of Changzhi Medical College Changzhi Shanxi China

Abstract

AbstractNicotinamide adenine dinucleotide phosphate (NADPH)‐diaphorase (N‐d) positive neurons have been extensively studied across various animals, and N‐d neurodegenerative neurites have been detected in some aged animal models. However, detailed knowledge on N‐d positivity and aging‐related alterations in the spinal cord and medulla oblongata of pigeons is limited. In this study, we investigated N‐d positivity and age‐related changes in the pigeon's spinal cord and medulla oblongata and compared them to those in rats and mice. Pigeons, had more N‐d neurons in the dorsal horn, around the central canal, and in the column of Terni in the thoracic and lumbar segments, with scattered neurons found in the ventral horn of the spinal segments. N‐d neurons were also present in the white matter of the spinal cord. Morphometric analysis revealed that the size of N‐d soma in the lumbosacral, cervical, and thoracic regions was substantially altered in aged pigeons compared to young birds. Furthermore, the lumbar to sacral segments underwent significant morphological alterations. The main findings of this study were the presence of age‐related N‐d positive bodies (ANB) in aged pigeons, predominantly in the external cuneate nucleus (CuE) and occasionally in the gracilis and CuEs. ANBs were also identified in the gracile nuclei and spinal cord in the aged rats and mice, whereas in aged rats, ANBs were detected in the CuE spinal nucleus. Immunohistochemistry showed that the age‐related alterations occurred in the cell types and neuropeptides in old animals. The results suggest weak inflammatory response and neuronal dysfunction in the spinal cord in aged pigeons. Our results suggested that the ANB could be a potential aging marker for the central nervous system.

Publisher

Wiley

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