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Many invertebrates are capable of renewing great parts of their body, while high-organized animals and humans can regenerate only some organs or their parts. The second rule: The regenerative ability is decreasing with age. The embryo has the capacity to undergo regulative growth when cells or tissues are removed or rearranged. In the adult, regeneration can only partially replace missing parts by growth and remodeling of somatic tissues. For example, while most of the mammals cannot regenerate limbs, many (including young children) can regenerate the ends of their fingers.
Hicklin and Wolpert [16] have linked the two potentials for the formation of head or foot structures with the term of positional value, implying that diffusible extracellular signals would account for axis patterning in Hydra. Coupled to theoretical considerations [17], these data were interpreted in terms of developmental potentials; the formation of head and foot is supposed to result from two pairs of antiparallel morphogenetic activation and inhibition gradients of extracellular signals [18].
Another successful attempt was reported by Rose in 1944 when he produced a small measure of regeneration of the amputated foreleg of the frog (a species that, despite folklore, is a nonregenerator) by dipping the extremity daily in hypertonic saline. Six years later, a similar result was reported by Polezhaev [10] in the same type of animal, by repeatedly needling the stump daily. Person et al. [11] described spontaneous regenerative responses following subtotal forelimb amputation in the young white rat.