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. 2018 Jan 25;6:6. doi: 10.3389/fped.2018.00006

Table 1.

Summary for the identification of all neuropathology abnormalities in the sudden infant death syndrome (SIDS) brainstem.

Reference Enzyme, transmitter, or receptor Level of brainstem SIDS cases Results
(17) An immunohistochemical method involving tyrosine hydroxylase Diencephalon, basal ganglia, midbrain, pons, and medulla oblongata 37 In SIDS, changes in basal ganglia can be induced via repeated ischemia or chronic hypoxia but can be associated with developing a neuronal system to the upper cardiorespiratory control
(18) 5-Hydroxytryptamines (5-HT) and 5-hydroxyindoleacetic acid High-performance liquid chromatography and Raphe obscure and PGCL 35 SIDS was related with lower TPH2 and 5-HT levels, consistent with a deficiency of medullary 5-HT disorder
(13) Immunohistochemical expression and substance P (SP) Neuromodulator 20 SP localized in fiber structures, with low to high densities
(19) 3H-nicotine 16 brainstem nuclei 27 In the brainstem alcohol and smoking adversely affect 3 H-nicotinic binding
(20) α7 and β2 Nicotinic acetylcholine receptors (nAChRs) Rostral medulla and pons 46 SIDS infants have a genetic defect acquired in the molecular regulation
(21) γ-Aminobutyric acid Medulla 24 SIDS may essential to include therapeutic agents that target more than one neurotransmitter system
(22) 1A (5HT1AR) Rostral medulla 67 In SIDS cigarette smoke and prone sleeping exposure support serotonergic brainstem system
(23) Serotonergic (5-HT) Respiratory nuclei and medulla 16 An outcome demonstrates that increased neurochemical preliminary evidence that supports boy’s vulnerability to SIDS
(24) Interleukin-2 and cytokine Cardiorespiratory- and sleep/arousal pathophysiology 18 The neuro-molecular disequilibrium results in the delicate molecular balance producing dysfunction in brainstem centers and disturbed homeostasis
(25) Pro-BDNF, rh-BDNF, and TrkB Rostral medulla 67 In the brainstem provides abnormal expression of rh-BDNF, TrkB, and pro-BDNF receptor protein of SIDS and non-SIDS infants
(26) Pontine Kolliker–Fuse nucleus and orexin receptors Raphe nuclei and locus coeruleus 28 KF neurons detection only 20% of SIDS