Vascular protecting agent having salt-absorption inhibitory activity
This invention provides a vascular protecting agent having salt-absorption inhibitory activity with the use of alginate oligosaccharide salt absorbed by the body via degradation to an oligosaccharide, so that a patient can easily and safely ingest such agent on a routine basis. A vascular protecting agent having salt-absorption inhibitory activity comprises, as an active ingredient, alginate oligosaccharide obtained by treating sodium alginate with a Pseudoalteromonas microorganism or a processed product thereof and/or a salt thereof.
1. A method for suppressing thickening of the blood vessel by inhibiting salt-absorption, which comprises administering an alginate oligosaccharide and/or salt thereof to a patient in need thereof, wherein the alginate oligosaccharide and/or salt thereof of formula 1:
wherein in formula 1,
R is a hydrogen atom or a metal ion;
R′ is a structure selected from the group consisting of G; G-G; M-G; G-G-G; G-G-M; G-M-G; G-M-M; M-G-G; M-M-G; and M-M-M, wherein the linkage among D-mannuronic acid (M) and L-guluronic acid (G) is α- or β-1,4-bound.
2. The method according to claim 1 , wherein the alginate oligosaccharide and/or salt thereof is obtained by treating sodium alginate with a Pseudoalteromonas microorganism.
3. The method according to claim 2 , wherein the Pseudoalteromonas microorganism is the Pseudoalteromonas sp. strain No. 1786.
4. A method for suppressing cardiac hypertrophy by protecting a vascular, which comprises administering an alginate oligosaccharide and/or salt thereof to a patient in need thereof, wherein the alginate oligosaccharide and/or salt thereof of formula 1:
wherein in formula 1,
R is a hydrogen atom or a metal ion;
R′ is a structure selected from the group consisting of G; G-G; M-G; G-G-G; G-G-M; G-M-G; G-M-M; M-G-G; M-M-G; and M-M-M, wherein the linkage among D-mannuronic acid (M) and L-guluronic acid (G) is α- or β-1,4-bound.
5. A method for suppressing renal hypertrophy and/or glomerular hardening by protecting a vascular, which comprises administering an alginate oligosaccharide and/or salt thereof to a patient in need thereof, wherein the alginate oligosaccharide and/or salt thereof of formula 1:
wherein in formula 1,
R is a hydrogen atom or a metal ion;
R′ is a structure selected from the group consisting of G; G-G; M-G; G-G-G; G-G-M; G-M-G; G-M-M; M-G-G; M-M-G; and M-M-M, wherein the linkage among D-mannuronic acid (M) and L-guluronic acid (G) is α- or β-1,4-bound.
6. The method according to claim 1 , wherein the alginate oligosaccharide and/or salt thereof is subcutaneously administered.
7. The method according to claim 4 , wherein the alginate oligosaccharide and/or salt thereof is subcutaneously administered.
8. The method according to claim 5 , wherein the alginate oligosaccharide and/or salt thereof is subcutaneously administered.
9. The method according to claim 4 , wherein the alginate oligosaccharide and/or salt thereof is obtained by treating sodium alginate with a Pseudoalteromonas microorganism.
10. The method according to claim 9 , wherein the Pseudoalteromonas microorganism is the Pseudoalteromonas sp. strain No. 1786.
11. The method according to claim 5 , wherein the alginate oligosaccharide and/or salt thereof is obtained by treating sodium alginate with a Pseudoalteromonas microorganism.
12. The method according to claim 11 , wherein the Pseudoalteromonas microorganism is the Pseudoalteromonas sp. strain No. 1786.