The effects of neonatal zingerone administration and adolescent alcohol exposure on bone health markers and morphometry in male Sprague–Dawley rats
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Wiley
Abstract
OBJECTIVE: Neonatal interventions influence long-term developmental outcomes, with excessive alcohol consumption impairing metabolism and bone health. Zingerone, a natural antioxidant, may possess health benefits against alcohol-induced oxidative damage and inflammation, promoting bone health. This study investigates the effects of zingerone on markers of bone turnover and morphometry in neonatal rats subjected to alcohol exposure during critical developmental stages.
METHODS: Ten-day-old male Sprague–Dawley rats (N = 35) were randomized and treated with water (C), zingerone (Z) (40 mg/kg), alcohol (A) (1 g/kg) or zingerone–alcohol combination (ZA) for 9 days. During adolescence, rats received either water or a secondary A insult (20% v/v) for 54 days. At termination, ELISA kits were used to measure biomarkers of bone formation (bone-specific alkaline phosphatase, osteocalcin, and procollagen Type I N-terminal propeptide). Bone morphology and morphometry was assessed using microcomputed tomography.
RESULTS: Neonatal zingerone (Z + A; ZA + A) and double alcohol exposure (A + A) significantly increased plasma BALP and P1NP levels (p < 0.05). Tibial length remained unchanged across groups (p > 0.05). Neonatal zingerone with adolescent alcohol (Z + A) significantly reduced tibial mass, bone mass-to-length ratios, and trabecular architecture near the growth plate (p < 0.05). Neonatal and adolescent administration of alcohol (A + A) significantly increased midshaft cortical thickness (p < 0.05).
CONCLUSION: Adolescent alcohol treatment impaired bone function and morphology, neonatal zingerone alone offering limited protection. Coadministration of zingerone with alcohol neonatally produced variable and context-dependent changes with no clear evidence of sustained protection against the effects of alcohol exposure. These findings underscore the importance of optimizing timing, dosage, and combination therapies for bone health. Further studies are warranted to clarify whether zingerone has clinically meaningful bone-protective effects.
Description
DATA AVAILABILITY STATEMENT : The data that support the findings of this study are available from the corresponding author upon reasonable request.
SUPPORTING INFORMATION: FIGURE S1 : Micro-CT workflow. FIGURE S2 : Illustration of the sections (3D VOI and 2D ROI) that were extracted from the tibia long bone samples for the analysis of bone microarchitecture using micro-CT imaging.
SUPPORTING INFORMATION: FIGURE S1 : Micro-CT workflow. FIGURE S2 : Illustration of the sections (3D VOI and 2D ROI) that were extracted from the tibia long bone samples for the analysis of bone microarchitecture using micro-CT imaging.
Keywords
Alcohol consumption, Bone health, Bone microarchitecture, Zingerone, Neonatal zingerone, Sprague–Dawley rats
Sustainable Development Goals
SDG-03: Good health and well-being
Citation
De Vos, B., Asiedu, B., Joubert, A.M., Kasonga, A.E. & Nyakudya, T.T. 2026, ‘The effects of neonatal zingerone administration and adolescent alcohol exposure on bone health markers and morphometry in male Sprague–Dawley rats’, BioMed Research International, vol. 2026, no. 1, art. 70605, pp. 1–10, doi:10.1155/bmri/7060593.
