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Effects of cyclodextrin‐iodopropane complex on methane production, ruminal fermentation and microbes, digestibility and blood metabolites in steers
Author(s) -
MOHAMMED Nazimuddin,
LILA Zeenat Ara,
TATSUOKA Noriko,
HARA Koji,
MIKUNI Katsuhiko,
HARA Kozo,
KANDA Shuhei,
ITABASHI Hisao
Publication year - 2004
Publication title -
animal science journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.606
H-Index - 38
eISSN - 1740-0929
pISSN - 1344-3941
DOI - 10.1111/j.1740-0929.2004.00167.x
Subject(s) - rumen , propionate , methanogenesis , chemistry , fermentation , digestion (alchemy) , zoology , dry matter , hay , urea , nutrient , food science , biochemistry , biology , chromatography , methane , organic chemistry
The effects when adding cyclodextrin‐iodopropane complex (CD‐IP) to a diet, on ruminal fermentation and microbes, digestibility, blood metabolites and methane production, were evaluated using four Holstein steers in a cross‐over design. The steers were fed Sudangrass hay plus concentrate mixture at a ratio 1.5:1, and CD‐IP (1% of dry matter) was given twice daily by mixing with concentrate mixture. Rumen and blood samples were collected at 0, 2, and 5 h after morning dosing. Ruminal pH and numbers of protozoa were unaffected by CD‐IP treatment. Ruminal molar proportion of acetate was decreased ( P  < 0.05), and propionate was increased ( P  < 0.01) at 2 h after CD‐IP dosing. Proportion of butyrate was increased ( P  < 0.05) and ammonia‐N was decreased ( P  < 0.05) at 2 and 5 h after CD‐IP dosing. Adding CD‐IP had no effect on the feed intake and digestion of nutrients. Plasma glucose was increased and urea‐N was decreased ( P  < 0.05) at 2 and 5 h after CD‐IP dosing. Methane production was decreased ( P  < 0.05) by approximately 18% in the treatment steers. Numbers of methanogenic bacteria were decreased ( P  < 0.05), while total viable counts, cellulolytic, sulfate reducing and acetogenic bacteria were unaffected. The present results are the first to show that CD‐IP can partially inhibit in vivo ruminal methanogenesis without adverse effects on digestion of nutrients.

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