Table 2.
3H‐nicotine binding to nicotine receptors (fmol/mg tissue) in selected brainstem nuclei in SIDS and control groups, adjusted for the effect of postconceptional age (PCA). Abbreviations: NTS = nucleus of the solitary tract; CEN = nucleus centralis medullae oblongata; HG = hypoglossal nucleus; PO = principal inferior olive; DAO = dorsal accessory olive; MAO = medial accessory olive; PBL = parabrachialis lateralis; PoO = nucleus pontis oralis; LC = locus coeruleus; GRPO = griseum pontis; IPN = interpeduncular nucleus; PAG = periaqueductal gray; CUN = nucleus cuneiformis; ICOL = inferior colliculus; RD = raphe dorsalis; RN = red nucleus.
Site | Age‐adjusted mean ± SE (n) | Diagnosis | Slope | P‐value | |
---|---|---|---|---|---|
SIDS | Controls | P‐value | |||
NTS | 7.0 ± 0.6 (22) | 5.7 ± 1.1 (6) | 0.313 | −0.12 | 0.003 |
CEN | 9.2 ± 0.8 (23) | 8.4 ± 1.5 (6) | 0.684 | −0.20 | <0.001 |
HG | 9.0 ± 0.8 (20) | 8.1 ± 1.4 (6) | 0.604 | −0.18 | 0.001 |
PO | 21.6 ± 1.1 (24) | 20.3 ± 2.1 (6) | 0.593 | −0.26 | <0.001 |
DAO | 11.8 ± 0.7 (22) | 11.9 ± 1.4 (6) | 0.956 | −0.19 | <0.001 |
MAO | 14.8 ± 1.0 (22) | 14.5 ± 1.9 (6) | 0.885 | −0.23 | 0.001 |
PBL | 12.3 ± 1.0 (21) | 11.0 ± 1.9 (6) | 0.551 | −0.24 | 0.001 |
PoO | 17.1 ± 1.2 (21) | 13.7 ± 2.3 (6) | 0.195 | −0.28 | 0.001 |
LC | 16.4 ± 1.3 (21) | 13.0 ± 2.3 (6) | 0.212 | −0.27 | 0.002 |
GRPO | 9.8 ± 0.8 (21) | 8.2 ± 1.5 (6) | 0.367 | −0.14 | 0.009 |
IPN | 20.1 ± 1.3 (20) | 15.9 ± 2.4 (6) | 0.144 | −0.25 | 0.006 |
PAG | 13.8 ± 1.2 (18) | 12.8 ± 2.1 (6) | 0.678 | −0.31 | 0.001 |
CUN | 15.3 ± 1.2 (19) | 12.5 ± 2.2 (6) | 0.274 | −0.29 | 0.001 |
ICOL | 10.2 ± 0.9 (18) | 8.5 ± 1.6 (5) | 0.378 | −0.21 | 0.002 |
RD | 15.5 ± 1.2 (17) | 12.6 ± 2.0 (6) | 0.228 | −0.24 | 0.003 |
RN | 17.5 ± 1.6 (19) | 14.5 ± 2.9 (6) | 0.376 | −0.35 | 0.002 |
Values are expressed as means ± SEM adjusted for PCA. No significant differences in 3H‐nicotinic receptor binding were found between the SIDS and control groups. P < 0.05, significant for either (i) diagnosis of SIDS vs. controls or (ii) the effects of PCA.