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Is ice cream a suitable carrier for probiotics?

Published online by Cambridge University Press:  04 June 2010

D. Wolvers ,
I. Mohede ,
E. Meynen ,
M. Vente-Spreeuwenberg ,
N. Johnson ,
J. Ueckert  and
R. Albers
D. Wolvers
Affiliation:
Unilever Research, Unilever Food and Health Research Institute, Olivier van Noortlaan 120, 3133 AT, Vlaardingen, The Netherlands
I. Mohede
Affiliation:
Unilever Research, Unilever Food and Health Research Institute, Olivier van Noortlaan 120, 3133 AT, Vlaardingen, The Netherlands
E. Meynen
Affiliation:
Unilever Research, Unilever Food and Health Research Institute, Olivier van Noortlaan 120, 3133 AT, Vlaardingen, The Netherlands
M. Vente-Spreeuwenberg
Affiliation:
Unilever Research, Unilever Food and Health Research Institute, Olivier van Noortlaan 120, 3133 AT, Vlaardingen, The Netherlands
N. Johnson
Affiliation:
Unilever Research, Unilever Food and Health Research Institute, Olivier van Noortlaan 120, 3133 AT, Vlaardingen, The Netherlands
J. Ueckert
Affiliation:
Unilever Research, Unilever Food and Health Research Institute, Olivier van Noortlaan 120, 3133 AT, Vlaardingen, The Netherlands
R. Albers
Affiliation:
Unilever Research, Unilever Food and Health Research Institute, Olivier van Noortlaan 120, 3133 AT, Vlaardingen, The Netherlands
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Abstract

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Proceedings of the Nutrition Society , Volume 69 , Issue OCE3: 3rd Immunonutrition Workshop, 21–24 October 2009, Girona, Spain , 2010 , E240
Copyright
Copyright © The Authors 2009

The objective of this study was to investigate the suitability of ice cream (IC) as a carrier for probiotics.

A DBRPC parallel study was performed with healthy 25–55 year old volunteers divided into three groups of 30. During 4 weeks, each group consumed either: (1) a daily IC control product, (2) IC with 1×109 cfu of Bifidobacterium lactis HN019 every day, or (3) IC with 5×109 cfu of B. lactis Bb-12 every other day alternating with control IC. Effects on the intestinal microflora and on phagocytosis, natural killer (NK) cell activity and faecal IgA were investigated.

During the four intervention weeks, the product stability of B. lactis Bb-12 was similar under laboratory controlled and home storage conditions, but loss of probiotic viability was 2–3-fold higher for B. lactis HN019 under home storage conditions.

Consumption of IC with B. lactis Bb-12 every other day resulted in the presence of a significant number of B. lactis in the faeces of study subjects compared to controls (P=0.0003), whereas every day consumption of IC with B. lactis HN019 did not increase numbers of the strain in faeces compared to control subjects (P=0.58). Sixty percent of subjects consuming the B. lactis Bb-12 product had the probiotic in their faeces. This is well within the range described for other product formats. In contrast, only 13% of HN019 consumers had detectable B. lactis in their faeces, whereas 10% of controls showed B. lactis positivity, which is similar to what has been described in the literature.

No shifts were detected in selected genera of the faecal microflora. Besides a very small but significant decrease in NK cell activity after consumption of either test product (P<0.04), no changes in immune markers were observed. The lack of beneficial effects on immune markers can be attributed to the fairly healthy study population and the fact that bifidobacteria are currently more and more positioned around gut and digestive health instead of immune health.

It was concluded that IC can be a suitable carrier for some, but not for all probiotics. B. lactis Bb-12 is compatible with IC delivering detectable amounts of live probiotics through the consumers intestine even in an every-other day consumption pattern.