TY - JOUR
T1 - Amino acids suppress apoptosis induced by sodium laurate, an absorption enhancer
AU - Takayama, Chie
AU - Mukaizawa, Fuyuki
AU - Fujita, Takuya
AU - Ogawara, Ken-ichi
AU - Higaki, Kazutaka
AU - Kimura, Toshikiro
PY - 2009/12
Y1 - 2009/12
N2 - The formulation containing sodium laurate (C12), an absorption enhancer, and several amino acids such as taurine (Tau) and L-glutamine (L-Gln) is a promising preparation that can safely improve the intestinal absorption of poorly absorbable drugs. The safety for intestinal mucosa is achieved because the amino acids prevent C12 from causing mucosal damages via several mechanisms. In the present study, the possible involvement of apoptosis, programmed cell death, in mucosal damages caused by C12 and cytoprotection by amino acids was examined. C12 induced DNA fragmentation, a typical phenomenon of apoptosis, in rat large-intestinal epithelial cells while the addition of amino acids significantly attenuated it. C12 alone significantly increased the release of cytochrome C, an apoptosis-inducing factor, from mitochondria, which could be via the decrease in the level of Bcl-2, an inhibiting factor of cytochrome C release. The enhancement of cytochrome C release by C12 led to the activation of caspase 9, an initiator enzyme, and the subsequent activation of caspase 3, an effector enzyme. On the other hand, Tau or L-Gln significantly suppressed the release of cytochrome C from mitochondria and attenuated the activities of both caspases, which could be attributed to the maintenance of Bcl-2 expression.
AB - The formulation containing sodium laurate (C12), an absorption enhancer, and several amino acids such as taurine (Tau) and L-glutamine (L-Gln) is a promising preparation that can safely improve the intestinal absorption of poorly absorbable drugs. The safety for intestinal mucosa is achieved because the amino acids prevent C12 from causing mucosal damages via several mechanisms. In the present study, the possible involvement of apoptosis, programmed cell death, in mucosal damages caused by C12 and cytoprotection by amino acids was examined. C12 induced DNA fragmentation, a typical phenomenon of apoptosis, in rat large-intestinal epithelial cells while the addition of amino acids significantly attenuated it. C12 alone significantly increased the release of cytochrome C, an apoptosis-inducing factor, from mitochondria, which could be via the decrease in the level of Bcl-2, an inhibiting factor of cytochrome C release. The enhancement of cytochrome C release by C12 led to the activation of caspase 9, an initiator enzyme, and the subsequent activation of caspase 3, an effector enzyme. On the other hand, Tau or L-Gln significantly suppressed the release of cytochrome C from mitochondria and attenuated the activities of both caspases, which could be attributed to the maintenance of Bcl-2 expression.
KW - Absorption enhancer
KW - Amino acids
KW - Apoptosis
KW - Caspase
KW - Cytochrome C
KW - Excipients
KW - Intestinal absorption
KW - Intestinal epithelia
KW - Sodium laurate
KW - Toxicity
UR - http://www.scopus.com/inward/record.url?scp=71649087231&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=71649087231&partnerID=8YFLogxK
U2 - 10.1002/jps.21757
DO - 10.1002/jps.21757
M3 - Article
C2 - 19630065
AN - SCOPUS:71649087231
SN - 0022-3549
VL - 98
SP - 4629
EP - 4638
JO - Journal of Pharmaceutical Sciences
JF - Journal of Pharmaceutical Sciences
IS - 12
ER -