Multiple effects of theobromine on fetus development and postnatal status of the immune system.

J Chorostowska-Wynimko, E Skopińska-Rózewska, E Sommer, E Rogala, P Skopiński, E Wojtasik
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Abstract

Caffeine and its active derivative, theobromine, are probably the most frequently ingested pharmacologically active substances. Considering their uninhibited transport via the placental barrier as well as immature enzymatic activities and metabolic pathways in embryos and infants resulting in the longer half-life of methyloxanthines and their accumulation, unrestrained uptake of these substances might result in noticeably more pronounced biological effects during pregnancy and the postnatal period. Our previous studies have shown that methyloxanthines are significant inhibitors of angiogenic growth factors production and angiogenesis itself. We have hypothesized that increased uptake of these substances might affect embryonal angiogenesis and, later in the postnatal period, maturation and functional activity of the offspring's immune system. The study was performed on 2-month-old Balb/c mice fed theobromine 2 or 6 mg/day during pregnancy and lactation. On day 18 of pregnancy the number and weight of embryos were assessed as was their tissue angiogenic activity, using the cutaneous angiogenesis assay. In the group of 4-week-old sucklings, body and spleen were weighed together with the trunk, and tail and limb length were measured. Six weeks after birth the splenocytes' mitogen-induced activity and their ability to induce graft-versus-host reaction as well as the humoral response to SRBC antigen were evaluated. Content of theobromine in the embryos' tissue was estimated by high liquid performance chromatography (HPLC). Theobromine feeding resulted in significant inhibition of embryo growth as assessed by their weight and decreased angiogenic activity of their tissue. The theobromine content in embryo tissue from treated groups was higher than in the controls, and the difference was close to significant. In the postnatal period the discrepancies in the treated 4-week-old group's development were also observed in the significantly shorter limbs in comparison to the controls. Moreover in the treated group of 6-week-old sucklings, considerable variations in the immune system's functional activity were registered as far as cellular and immune response were concerned. Respectively, the splenocytes' mitogen-induced proliferative activity was significantly suppressed while the graft-versus-host reaction was up-regulated, and the serum antibodies titer was elevated in correspondence to the observed spleen enlargement. We concluded that a theobromine-enriched diet affects progeny development in both prenatal and postnatal periods. Consequently, particular attention should be paid to the reduction of theobromine consumption, and most probably that of other methyloxanthines, during pregnancy and lactation.

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可可碱对胎儿发育和出生后免疫系统的多重影响。
咖啡因及其活性衍生物可可碱可能是最常被摄入的药理活性物质。考虑到甲基黄嘌呤通过胎盘屏障的不受抑制的运输,以及胚胎和婴儿体内未成熟的酶活性和代谢途径,导致甲基黄嘌呤半衰期更长并积累,这些物质的不受限制的摄取可能导致妊娠期和产后明显更明显的生物效应。我们之前的研究表明,甲基黄嘌呤是血管生成生长因子产生和血管生成本身的重要抑制剂。我们假设这些物质的摄取增加可能会影响胚胎血管生成,并在出生后影响后代免疫系统的成熟和功能活动。研究对象是两个月大的Balb/c小鼠,在妊娠和哺乳期每天喂食2或6毫克可可碱。在妊娠第18天,用皮肤血管生成试验评估胚胎的数量和重量以及组织血管生成活性。4周龄乳牛组称重体、脾及躯干,测量尾、肢长。出生6周后,评估脾细胞诱导丝裂原的活性、诱导移植物抗宿主反应的能力以及对SRBC抗原的体液反应。采用高效液相色谱法测定胚胎组织中可可碱的含量。可可碱喂养对胚胎生长有明显的抑制作用,这是通过它们的体重来评估的,并降低了它们组织的血管生成活性。各处理组胚胎组织中可可碱含量均高于对照组,差异接近显著。在出生后,与对照组相比,4周大组的四肢发育也明显缩短。此外,就细胞和免疫反应而言,在6周龄哺乳动物的治疗组中,免疫系统功能活性发生了相当大的变化。脾细胞有丝分裂原诱导的增殖活性被显著抑制,移植物抗宿主反应被上调,血清抗体滴度随脾脏增大而升高。我们的结论是,富含可可碱的饮食在产前和产后都会影响后代的发育。因此,应特别注意在怀孕和哺乳期减少可可碱的消耗,并很可能减少其他甲基黄嘌呤的消耗。
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